- Research article
- Open Access
A novel RNA binding protein affects rbcL gene expression and is specific to bundle sheath chloroplasts in C4plants
BMC Plant Biology volume 13, Article number: 138 (2013)
Plants that utilize the highly efficient C4 pathway of photosynthesis typically possess kranz-type leaf anatomy that consists of two morphologically and functionally distinct photosynthetic cell types, the bundle sheath (BS) and mesophyll (M) cells. These two cell types differentially express many genes that are required for C4 capability and function. In mature C4 leaves, the plastidic rbcL gene, encoding the large subunit of the primary CO2 fixation enzyme Rubisco, is expressed specifically within BS cells. Numerous studies have demonstrated that BS-specific rbcL gene expression is regulated predominantly at post-transcriptional levels, through the control of translation and mRNA stability. The identification of regulatory factors associated with C4 patterns of rbcL gene expression has been an elusive goal for many years.
RLSB, encoded by the nuclear RLSB gene, is an S1-domain RNA binding protein purified from C4 chloroplasts based on its specific binding to plastid-encoded rbcL mRNA in vitro. Co-localized with LSU to chloroplasts, RLSB is highly conserved across many plant species. Most significantly, RLSB localizes specifically to leaf bundle sheath (BS) cells in C4 plants. Comparative analysis using maize (C4) and Arabidopsis (C3) reveals its tight association with rbcL gene expression in both plants. Reduced RLSB expression (through insertion mutation or RNA silencing, respectively) led to reductions in rbcL mRNA accumulation and LSU production. Additional developmental effects, such as virescent/yellow leaves, were likely associated with decreased photosynthetic function and disruption of associated signaling networks.
Reductions in RLSB expression, due to insertion mutation or gene silencing, are strictly correlated with reductions in rbcL gene expression in both maize and Arabidopsis. In both plants, accumulation of rbcL mRNA as well as synthesis of LSU protein were affected. These findings suggest that specific accumulation and binding of the RLSB binding protein to rbcL mRNA within BS chloroplasts may be one determinant leading to the characteristic cell type-specific localization of Rubisco in C4 plants. Evolutionary modification of RLSB expression, from a C3 “default” state to BS cell-specificity, could represent one mechanism by which rbcL expression has become restricted to only one cell type in C4 plants.
The highly efficient C4 pathway of photosynthetic carbon assimilation is utilized by less than 5% of terrestrial plants, and yet C4 plants account for about a fourth of the earth’s primary productivity [1–4]. The enhanced photosynthetic capabilities of C4 plant species allow them to out-compete more common and less efficient C3 species. This is most evident in areas of high temperature and/or low water availability, conditions under which C4 plants typically thrive. In spite of their much higher productivity, there are only a few C4 plant species utilized as crops for food and biofuel production, the most notable being maize and sugarcane [1–4]. Understanding the specialized developmental, molecular, and biochemical processes responsible for C4 function is a significant focus of photosynthesis and agricultural research. Agricultural benefits include contributing to the development of non-agricultural C4 plants that are more amenable to agricultural usage, understanding mechanisms of plant adaption to extreme arid conditions, and possibly enabling the engineering of C4 characteristics into C3 crop species [1–5]. As a unique developmental system, the specific localization of key photosynthetic enzymes to one cell type, but not in another adjacent cell type within a small localized leaf region, provides a unique opportunity to address molecular mechanisms underlying the selective compartmentalization of gene expression in plants [5, 6].
Characteristics common to all C4 species include utilization of phosphoenolpyruvate carboxylase (PEPCase) as the initial primary CO2 fixation enzyme and production of C4 acids by a first stage of reactions, followed by decarboxylation of C4 acids, and subsequent re-fixation of released CO2 by Rubisco (Calvin cycle) in a second stage. Through the partitioning of Rubisco, C4 plants reduce or eliminate the photosynthetically wasteful reactions of photorespiration, thereby enhancing their CO2 fixation ability [3, 5–9]. C4 plants typically possess kranz-type leaf anatomy consisting of two distinct photosynthetic cell types, bundle sheath (BS) cells and mesophyll (M) cells [3, 5–10]. Although some variations have been identified (such as the less common single cell C4 photosynthesis), in most C4 leaves the BS cells occur as a layer around each leaf vein, with one or more layers of M cells surrounding each ring of BS cells [5–10]. This specialized leaf anatomy provides a structural framework that compartmentalizes the two stages of C4 carbon assimilation. Together these serve as a “CO2 pump” that concentrates CO2 within BS cells, where Rubisco is localized. Photosynthesis in kranz-type C4 leaves requires the cell-type specific expression of genes encoding certain CO2 assimilation enzymes, such as Rubisco in BS cells and PEPCase in M cells [5–7, 11]. This two-cell compartmentalization and associated cell-type specificity in gene expression does not occur in C3 plants, which possess only one photosynthetic cell type, and where the initial CO2 fixation enzyme is ribulose-1,5-bisphosphate carboxylase (Rubisco).
In spite of the clearly defined biological parameters and advantages associated with C4 plants (cell-type specific expression, anatomical and metabolic modifications, increased nitrogen-use efficiency, adaptability to marginal habitats), molecular processes responsible for C3 versus C4 photosynthetic gene expression patterns have remained highly elusive for many years. Previous studies have shown that both transcriptional and post-transcriptional regulation are involved in BS or M cell-specific regulation of C4 genes [5–7, 11, 12]. While there are many trans-acting proteins known to be associated with the expression of plastidic- and nuclear-encoded photosynthetic genes at all regulatory levels in both C3 and C4 plants [5, 6, 12–17], most of these are not directly implicated in determining BS versus M cell-specific gene expression. Some of the few transcription factors shown to be associated with C4 development are members of the Golden 2-like (GLK) gene family [5, 11, 12]. One member of this family, Golden2 (G2) is a transcriptional regulator that functions primarily within BS cells and affects the overall development of these cells in maize leaves. A paralog of this gene, Glk1, is abundantly expressed in M cells, where it also regulates overall photosynthetic development. Recently, it was demonstrated that a transcription factor encoded by the Scarecrow (Scr) gene is associated with the normal development of kranz leaf anatomy, affecting the morphology and plastid content of maize leaf BS cells . While each of these transcription factors has significant effects on BS or M cell development, direct regulation of C4 photosynthetic gene expression within their respective cell types has not been demonstrated [5, 11, 12, 18]. In fact, to date no trans-acting factors have been directly associated with the BS versus M cell-specific regulation of any individual C4 gene.
As the principle enzyme of photosynthetic carbon fixation, Rubisco is central to the viability, growth, and productivity of all plants. Understanding regulatory processes responsible for the production of Rubisco specifically within the leaf BS cells of C4 plants, and how these processes differ from the “default” C3-type form, is highly significant for understanding the molecular basis of this specialized photosynthetic pathway [5, 7, 11, 12]. Rubisco is located within the chloroplasts of all plants, and is composed of eight large (LSU, 51–58 kDa) and eight small (SSU; 12–18 kDa) subunits [7, 19, 20]. The rbcL gene encoding the LSU is transcribed and translated within the chloroplasts. The SSU, encoded by a nuclear RbcS gene family, is translated on cytoplasmic ribosomes as a 20-kDa precursor that is targeted to the plastids. The rbcL and RbcS transcripts and corresponding proteins are highly abundant and coordinately regulated; the two subunits accumulate in stoichiometric amounts within the plastids [5–7, 19, 20]. Rubisco gene expression in C4 and C3 plants is influenced by many factors, including light, development, cell type, photosynthetic activity, and even pathogen infection [5–7]. In addition to transcriptional control, many aspects of rbcL and RbcS expression have been shown to be controlled through mRNA processing (degradation or stabilization of transcripts) and regulation of translation. Significantly, many studies have demonstrated that in several dicot and monocot C4 species, including amaranth, flaveria, cleome, and maize, post-transcriptional control plays a key role in determining the BS cell-specific expression of genes encoding both Rubisco subunits [5, 7]. Post-transcriptional control of cell-type specificity for rbcL and RbcS in C4 plants is very stringent; even when these genes are ectopically over-expressed in maize, Rubisco accumulation remains highly specific to BS cells .
Plastid- and nuclear-encoded mRNAs possess specific cis-acting sequences that mediate their post-transcriptional regulation [6, 13–17, 22]. Cis-acting control regions can occur within the 5′ UTR, the 3′ UTR, or even the coding region of an mRNA. For plastid-encoded mRNAs, where post-transcriptional regulation is the primary regulatory determinant, nuclear-encoded proteins usually interact specifically with 5′ or 3′ UTR sequences to regulate one or more aspects of mRNA metabolism. There are a very large number of nuclear-encoded RNA binding proteins in plastids, reflecting the very large number of complex RNA metabolic processes that occur for each of the 100 or so plastid-encoded transcripts [14, 16, 17]. RNA modifications can include processing of 5′ and 3′ termini, intron splicing, proofreading and editing, as well as regulation of translation and stability. Several classes of RNA binding proteins have been identified and characterized in chloroplasts, many of which are highly specific for unique sequences contained within different plastid-encoded mRNAs [14, 16, 17, 23, 24]. Among these, the most predominant are the pentatricopeptide repeat (PPR) family of RNA binding proteins, with about 450 members in higher plants [16, 17, 25]. One PPR protein has been shown to define 5′- processing of rbcL mRNA .
This current study contributes a new member to the list of plastid-targeted RNA binding proteins that affect gene expression in chloroplasts, in this case through its selective interaction with rbcL mRNA. The RBCL RNA S1-BINDING DOMAIN protein (RLSB) was isolated from chloroplasts of a C4 plant by affinity-purification based on its ability to bind rbcL mRNA in vitro. This protein, encoded by the RLSB gene, is present and highly conserved among a wide variety of plant species, contains a conserved S1 RNA binding domain, and a plastid transit sequence. We show here that RLSB affects rbcL gene expression within BS chloroplasts of C4 maize (Zea mays), as well in C3Arabidopsis (Arabidopsis thaliana) chloroplasts. Mutation or silencing of RLSB led to clearly observable changes in levels of rbcL mRNA and LSU protein accumulation, with many associated developmental effects. This is the first cell-type specific regulatory factor to be implicated in the regulation of an individual photosynthetic gene in a C4 plant, its accumulation correlating tightly with the BS-specific expression of the plastidic rbcL gene that it regulates. This strong correlation suggests that modifications of RLSB gene expression from the “default” C3 pattern to C4-type BS cell-specificity, and associated cell-type specific localization of rbcL expression, might represent one evolutionary process enabling C4 expression patterns in plants that utilize this specialized pathway for photosynthetic carbon assimilation.
Isolation of an rbcL mRNA binding protein from chloroplasts of a C4plant
Our earlier studies identified four sites of highly specific RNA-protein interactions at the 5′ region of rbcL mRNA in plastid extracts from the C4 dicot amaranth . These were found only in light-grown plants, when Rubisco synthesis occurred, and not in etiolated plants, when Rubisco synthesis did not occur. We hypothesized that RNA-protein interactions such as these might be involved in regulating BS cell-specific rbcL gene expression, as well as light-mediated regulation, in the leaves of C4 plants. Two types of RNA “bait” molecules were used for affinity purification of chloroplast proteins that specifically interact with rbcL 5′ RNAs ; an in vitro-transcribed RNA corresponding to rbcL 5′ RNA of the C4 dicot amaranth, a region previously shown to interact with plastidic proteins in vivo (beginning at the 5′ end of the processed rbcL mRNA at −66 and extending to +60 in the coding region), and a control 7Z-AS RNA, a yeast viral 3′ UTR of similar size and AU content [26, 27]. These transcripts were biotin-tagged at the 3′ end to allow binding of the RNA to streptavidin magnetic beads (Figure 1A). The 5′ RNA-biotin-streptavidin beads were incubated with plastid extracts prepared from leaves of the C4 plant amaranth, using preparatory and binding conditions previously optimized for these leaves . The bead-bound RNA-protein complexes were washed and isolated by magnetic separation. Figure 1B shows affinity purified plastid proteins after incubation with rbcL or control RNAs, separated and visualized by SDS-PAGE.
At least six distinct affinity-purified proteins were specifically captured with rbcL 5′ RNA, and not with the control viral RNA, ranging in size from 30–70 kDa (Figure 1B). Analysis of tryptic peptide sequences using Maldi-Tof mass spectrometry (Custom Biologics, Toronto, CA) indicated that one of the purified proteins (p44, red arrow in Figure 1B) had similarity to proteins in the database containing a plastid transit sequence and a conserved S1 RNA binding domain (Figure 1C, Additional file 1: Figure S1). Taken together, these characteristics identified p44 as a potential rbcL-mRNA binding protein in chloroplasts. This protein, now designated as RLSB, was selected for further analysis. The sequence and characteristics of the Arabidopsis ortholog are indicated in Figure 1C.
Highly similar orthologs of the RLSB protein were identified in more than 15 plant species including dicots, monocots, C3 and C4 species. This includes Bienertia sinuspersici (Gerald Edwards, personal communication), a dicot plant species that utilizes a unique single-cell form of C4 photosynthesis . Comparative alignments of representative protein sequences are shown in Additional file 1: Figure S1 and Additional file 2: Figure S2. Overall similarities among the plant species examined range from 60% for maize-Arabidopsis, to 70% for maize-rice, and 90% for maize-sorghum. All of these proteins have putative plastid-targeting sequences. RLSB appears to be encoded from a single copy gene in all of the species examined.
RLSB is specific to BS cells in C4leaves
The binding affinity of RLSB to rbcL mRNA in extracts from C4 chloroplasts presented the possibility that this binding activity might be associated with rbcL regulation within BS cells. If RLSB is in fact closely associated with active rbcL gene expression, then it would be expected that this RNA binding protein, like Rubisco, would also show specificity to BS chloroplasts in the mature leaves of Kranz-type C4 plant species. Immunolocalization analysis was performed with three C4 species shown in Figure 2; the dicot Flaveria bidentis (Figure 2 column 1; 3A, 3B, 3C), the monocot maize (Figure 2 column 2; 3D, 3E, 3F) and the monocot Setaria viridis (Figure 2 column 3, 3G, 3H, 3I). In the leaves of each of these C4 species, RLSB (Figure 2 top row: 3A, 3D, 3G) co-localized with Rubisco LSU (Figure 2 middle row; 3B, 3E, 3H) specifically within chloroplasts of the leaf BS cells. The sections used for Figure 2 were all taken from mature leaves (midway between the base and tip) of the indicated plant species, reacted with the primary and secondary antisera indicated, and captured using confocal imaging. Note that in F. bidentis, the RLSB/LSU containing chloroplasts were at the centripetal position within the BS cells (adjacent to the vascular centers), as is characteristic for this C4 dicot . In maize and S. viridis, the BS chloroplasts were at the centrifugal portion (away from the vascular center), as expected for these C4 monocots . Very low levels of 564–577 nm emission were also observed in M cell chloroplasts of sections reacted with RLSB antisera; from this imaging we cannot determine if this was due to very low levels of RLSB accumulating in these cells, or perhaps to background reactions of the affinity-purified RLSB antisera. RLSB does not appear to be an abundant protein, and sensitivity for detection needed to be increased, relative to LSU, for its fluorescent detection. As a control, the MP cell-specific enzyme PEPCase was localized specifically to the cytoplasm of leaf M cells of all three C4 species (Figure 2 bottom row; 3C, 3F, 3I).
To confirm that RLSB does not accumulate in the C4 M cells, mechanical separation of BS and M cells from wild type maize B73 was performed using the leaf rolling method . This yielded a highly purified population of M cells, as well as a population that was enriched for BS cells but also contained M cells (B/m). Immunoblot analysis clearly demonstrated that RLSB, together with LSU, was present in soluble protein extracts prepared from the B/m cells, but were not detectable in extracts from the purified M cells (Figure 2, panels on the right). As a control, PEPCase was very abundant in the purified M extracts, and was also present, at slightly reduced levels, in the B/m cell extracts. It should be noted that the B/m extracts were isolated immediately after rolling out the M cells, without any additional purification steps. We have observed that RLSB degrades rapidly once the leaves have been disrupted; thus this cell population was not subjected to any further purification, leaving a significant amount of M cells remaining in the B/m extracts. The “rolled out” M cell population itself was free of contaminating BS cells, as determined by the lack of LSU in these protein extracts. These findings, together with the immunolocalization analysis, confirm that RLSB is highly specific to BS cells in the leaves of maize and other C4 plants.
Specificity of RLSB binding and effects of rlsb-insertion mutation in the C4monocot maize
Although RLSB was first identified from chloroplast extracts of the C4 dicot Amaranth, it’s very strong conservation across many different plant species made it feasible to employ the model C4 plant maize (Zea mays) for functional characterization. The numerous genetic and database resources available for maize allowed for mutational, developmental, and molecular analysis of RLSB in a plant with a well-defined genetic background. Some of the resources utilized for this study include those described in [30–33], as well as the Maize Photosynthetic Mutant (PML, http://pml.uoregon.edu/photosyntheticml.html), and The Plant Proteome Database (PPDB; proteomics data for the maize RLSB ortholog can be viewed at http://ppdb.tc.cornell.edu/dbsearch/gene.aspx?id=674610).
In vitro affinity purification of RLSB from C4 chloroplast extracts provided initial evidence for its selective interaction with rbcL mRNA. To determine if RLSB binds specifically to rbcL mRNA in vivo, we used RNA immunopurification with RLSB antisera and quantitative real-time PCR (RIP/qRT-PCR) (Figure 3). Recent studies have demonstrated the enhanced reliability and quantitative accuracy of this approach for analyzing specific protein-RNA associations, with a higher degree of enrichment, lower background, and greater dynamic range than previously used methods such as RIP-Chip (for example [34, 35]). RLSB was immunoprecipated from chloroplast extracts prepared from leaves of wild type maize line B73 . RNA was purified from the pellet fractions, and qRT-PCR was performed using primers for rbcL and, for comparison, the representative plastid-encoded transcripts psaB, psbA, petD, psaC, atpA, and atpB, as indicated in Figure 3. As controls, RIP/qRT-PCR reactions were performed using antisera against cytoplasmic PEPCase, and with no added antisera. All of the qRT-PCR reactions were standardized relative to plastid-encoded rpl2 mRNA (encodes ribosomal protein Rpl2).
Strong selective association of rbcL mRNA with RLSB was observed in the maize chloroplast extracts (Figure 3). Of the seven plastid-encoded mRNAs examined, only sequences corresponding to rbcL mRNA showed high levels of amplification from the anti-RLSB pellet fraction (4.2 fold above background, as determined from the no-added antibody control reactions). Three plastid-encoded mRNAs (psaB, petD, psaC) showed no amplification above background from the immunopurified RLSB pellets. Three other plastid-encoded transcripts (psbA, atpA, and atpB) showed only very slight levels of amplification (0.2 – 0.3 fold above the averaged background value). None of these sequences, including rbcL, were amplified from control PEPCase immunopurifications, or when no antisera was used (Figure 3). It is clear from this analysis that rbcL mRNA showed significantly greater interaction with RLSB than any of the other representative plastidic mRNAs tested. These findings confirm that the plastid-localized RLSB protein does in fact bind to plastid-encoded rbcL mRNA in vivo, with significant specificity for rbcL mRNA in wild type maize plastids.
The biological significance of RLSB interactions with rbcL mRNA in maize was investigated by making use of Mu transposon insertion mutations within the maize genomic RLSB ortholog. The genomic sequence of the maize RLSB ortholog was initially identified (within maize Genomic BAC AC211368.4) using a cDNA sequence accession #BT035293.1 (partial sequence; the full length cDNA is accession #JX650053, Additional file 1: Figure S1 and Additional file 2: Figure S2). This gene (GRMZM2G087628) is approximately 3540 nucleotides in length, with seven introns (Additional file 3: Figure S3). Mu insertions into this gene were identified by screening the maize Photosynthetic Mutant Library (PML) at the University of Oregon (http://pml.uoregon.edu/photosyntheticml.html), using primer sets specific for RLSB and the Mu transposon borders (see Methods). Two independent lines were isolated and designated as rlsb-1 and rlsb-2. Genomic mapping from both ends of the Mu transposon indicates that each line contains a single insert within the RLSB gene, located within the first exon; these occur at positions just 37 nt apart. The insertion in rlsb-1 is nearly adjacent to the 5′ splice site of intron 1, positioned 8 nt upstream of the first 5′ intron junction. The insertion in rlsb-2 is positioned 45 nucleotides upstream of the first splice junction (red stars in Additional file 3: Figure S3). Both Mu insertions occur within a protein coding exon, and would affect the mature RLSB protein within its N-terminal portion, just after the predicted cleavage site for the plastid transit sequence. When homozygous, the phenotype of each line is identical; the leaves start out as virescent-yellow, and gradually begin to green from the tip to the base as they grow and develop (Additional file 4: Figure S4, Top panels). The mutants grow more slowly than wild type, so that leaf development is delayed approximately one day. Genetic crosses demonstrate that the two mutants do not complement; most of the experiments presented here were done using rlsb-1/rlsb-2 double mutants.
An analysis of these maize insertion mutants must be undertaken within the framework of the maize leaf developmental gradient. A maize leaf originates and grows outward primarily from an intercalary meristem located at the base of the leaf [36, 37]. This leads to the development of a linear gradient of cells occurring along the entire length of a growing maize leaf, with younger cells occurring at the lower (basal) regions, and older cells at the outer (towards the tip) regions. Rubisco mRNA and protein accumulation increase along this maize leaf gradient, with the transcripts appearing slightly ahead of their corresponding proteins [5, 7]. In illuminated maize leaves, Rubisco mRNAs and subunit proteins are specifically localized to BS precursors at their first occurrence, and remain specific to BS cells across the entire developmental gradient.
The phenotype of these RLSB insertion mutants indicates that rlsb-1 and rlsb-2 affect early photosynthetic development, as observed in lower regions of the maize leaf (Additional file 4: Figure S4, Top Panels). An overview of total protein accumulation (soluble plus membrane) demonstrated that the overall protein profiles were mostly similar for both RLSB insertion mutant (rlsb-1/rlsb-2) and non-insertion mutant (RLSB/RLSB) leaves in the lower leaf regions (lower 1/3 of the leaf, earlier developmental stage), although there were clearly differences in levels for a few proteins bands (Figure 4A). Some of these were decreased in lower regions of the mutant leaves, while others were increased (indicated in Figure 4A). Most notably, protein bands migrating at the position of the Rubisco LSU and SSU were significantly reduced in lower regions of the rlsb-1/rlsb-2 leaves, relative to RLSB/RLSB. At the leaf upper regions (upper 1/4 of the leaf, more advanced developmental stage), levels of the Rubisco protein bands were elevated, so that identical amounts were present in this portion of the mutant and non-mutant leaves. Similarly, in rlsb-1/rlsb-2 leaves, protein bands that were altered in lower regions were present at normal RLSB/RLSB levels in the upper regions. Thus, at this level of analysis, insertion mutants of RSLB had different effects on protein accumulation in the lower versus the upper portion of the maize leaf.
Reductions in Rubisco LSU levels in lower regions of the rlsb-1/rlsb-2 leaves were more clearly discernible when soluble proteins were analyzed separately (Figure 4B). As with total proteins (Figure 4A), soluble protein profiles were mostly similar for rlsb-1/rlsb-2 mutant and RLSB/RLSB leaves. We detected at least 3 prominent soluble proteins, in addition to the dramatically reduced LSU, that were clearly reduced in lower leaf regions of the mutant plants. Several differences in protein composition were also observed for membrane-bound proteins in the lower leaf regions of mutant plants (not shown). These differences in accumulation of the LSU and other proteins between RLSB mutant and non-mutant plants were not observed at the leaf upper regions (not shown). In plants heterozygous for the rlsb mutation (RLSB/rlsb-1, RLSB/rlsb-2), accumulation of LSU (and the other indicated proteins) was not affected in either leaf region; the protein profiles for these plants were identical to RLSB/RLSB (Figure 4B), demonstrating that the insertion mutant is recessive.
Reductions in LSU protein accumulation were accompanied by reduced in vivo synthesis of the LSU protein in the lower region of the mutant leaves, but not in the upper region (Figure 4C, top and middle panels). Incubation of leaf disks from rlsb-1/rlsb-2 and RSLB/RSLB plants with 35S-met/cys labeling solution for one hour, followed by isolation of soluble proteins and separation of equalized protein samples by SDS-PAGE, showed greatly reduced in vivo synthesis of the LSU protein in lower regions of the mutant leaves (Figure 4C, top panel). While significant differences in synthesis were found for the LSU protein in the lower regions, the majority of proteins observable in the labeled extracts showed no differences between rlsb-1/rlsb-2 and RLSB/RLSB. This mostly selective reduction in LSU synthesis was not observed in the upper regions. Immunoprecipitation of LSU protein confirmed that LSU synthesis was significantly reduced in the lower regions, but not the upper regions, of the rlsb-1/rlsb-2 mutant maize leaves (Figure 4C, middle panel). As demonstrated by immunoblot analysis using RLSB antisera (Figure 4C, bottom panels), greatly reduced levels of in vivo LSU synthesis in lower regions of the rlsb-1/rlsb-2 leaves correlated very closely with reduced levels of RLSB protein accumulation at these same regions. Comparatively, the upper regions of the rlsb-1/rlsb-2 leaves, and both regions of RLSB/RLSB leaves, all showed much higher levels of RLSB protein accumulation, corresponding with their higher levels of LSU synthesis.
The combined data of Figure 4 indicate that the accumulation and synthesis of Rubisco LSU protein was delayed, and not completely eliminated, in the rlsb-1/rlsb-2 maize leaves. The loss or reduction of the RLSB mRNA binding protein was accompanied by reduced production of the Rubisco LSU protein, as well as the other observable effects, only during early leaf development in the lower leaf region. As developmental age advanced along the maize leaf gradient, the effects of this mutation appear to be attenuated, so that in the more developmentally advanced outer leaf regions, LSU synthesis and accumulation reached normal levels.
Immunoblot analysis confirmed the reduced accumulation of both Rubisco LSU protein and RLSB proteins in lower regions of the rlsb-1/rlsb-2 maize leaves. Relative to the same region of RLSB/RLSB leaves, LSU was reduced approximately 12–15 fold in the rlsb-1/rlsb-2 plants (Figure 5A, top panel, based on phosphorimager software analysis). RLSB was not detectable in the rlsb-1/rlsb-2 leaf lower regions using these same conditions (Figure 5A, middle panel). A digitally enhanced image of the middle panel of Figure 5A demonstrates that RLSB did in fact accumulate in the lower leaf regions of rlsb-1/rlsb-2 mutants, but at greatly reduced levels (Additional file 5: Figure S5, top panel). In fact, this longer exposure reveals that one of the rlsb-1/rlsb-2 mutants had slightly higher levels of RLSB, relative to a different rlsb-1/rlsb-2 mutant (compare the second and fourth lanes of Additional file 5: Figure S5, top panel). This was correlated closely with slightly higher levels of LSU for this same plant (compare the second and fourth lanes of Figure 5A, top panel).
Analysis of mRNA levels using qRT-PCR indicated in RLSB/RLSB maize leaves, rbcL mRNA was present at much higher levels than RSLB mRNA (Figure 5B). In fact, rbcL transcripts were more than 150-fold more abundant (note the difference Y-axis scales in Figure 5B). This difference in relative levels of the two mRNAs may not reflect respective levels of protein accumulation in the RLSB/RLSB maize leaves, since both RLSB and LSU were easily detected with similar exposure levels of the immunoblots. In lower portions of the rlsb-1/rlsb-2 mutant maize leaves, both rbcL and RLSB transcript levels were correspondingly reduced (3.5-4.5 fold, respectively) relative to the same region of RLSB/RLSB leaves (Figure 5B). Thus, insertion mutagenesis of RLSB reduced but did not completely eliminate RLSB and rbcL expression, allowing for low but still detectable levels of both mRNAs to accumulate in lower rlsb-1/rlsb-2 leaf regions. The fact that mRNA levels for both transcripts were reduced in approximate coordination further supports a regulatory connection between RLSB and levels of rbcL gene expression, involving regulation at the level of rbcL mRNA accumulation. Furthermore, it is notable that the reduced levels of RLSB and rbcL transcripts in the lower leaf regions of rlsb-1/rlsb-2 plants were not reflective of actual RLSB and LSU protein accumulation. Most significantly, LSU protein levels were reduced more dramatically than rbcL mRNA in lower regions of the rlsb-1/rlsb-2 mutant leaves (12–15 fold versus approximately 4-fold, respectively), suggesting that utilization of the rbcL mRNA for translation was also affected by reduced RLSB.
While RLSB shows strong selectivity in binding to rbcL mRNA, the effects of the rlsb-1/rlsb-2 mutation extend beyond this single plastid gene. In addition to LSU, lower leaf regions of the double mutants showed significant reductions in the accumulation of several representative plastid- and nuclear-encoded proteins (Figure 6). Also similar to LSU, the reductions described below occurred only in the lower leaf regions of rlsb-1/rlsb-2 plants; in the upper leaf regions, levels had recovered to those of RLSB/RLSB leaves (data not shown). Decreased RLSB in lower regions of the rlsb-1/rlsb-2 leaves was associated with reductions of five other representative plastid-encoded proteins (Figure 6, left panel). PsaB, PsaC, PsbA, and CF1αβ all showed rlsb-1/rlsb-2 mutation-associated reductions that were similar to or greater than LSU (compare Figures 5A and 6). Although there was a trend for some chloroplast-encoded transcripts to have reduced accumulation in the rlsb-1/rlsb-2 lower leaf regions (Additional file 6: Figure S6A), these reductions were not as dramatic as the protein reductions observed. The most significant reduction occurred for petD (three-four fold); reductions in psaB, psaC, and atpB, while statistically significant, were less than two fold. Transcripts for psbA, atpA and rpl2 showed no significant reductions. Thus, within the chloroplast itself, reductions in RLSB levels were accompanied by consistent drop in levels of many photosynthetic proteins, with variable reductions in levels of different plastid-encoded mRNAs. Plastid-encoded ribosomal RNAs also showed a slight, but not statistically significant, reduction in accumulation in the affected rlsb-1/rlsb-2 leaf regions (Additional file 6: Figures S6B and S6C). Severe reductions in protein accumulation such as these, together with moderate reductions in the accumulation of some mRNAs, might be consistent with a more global effect on plastic translation, as described for maize ribosome assembly mutants . However, the lack of any significant effect on ribosomal rRNAs, as would occur be in the case of a general translation mutation, makes it highly unlikely that RLSB would be a member of this class of basic translational regulators. In addition, it is important to consider that, while RLSB is specific to BS cells, all of the other plastid-encoded proteins that were affected would normally accumulate in both BS and M cells, with the photosystem II-associated PsbA protein in fact being most abundant in M plastids [5, 11, 39]. It therefore also highly unlikely that the reduced levels of PsbA, PsaB, PsaC, and CFαβ in the rlsb-1/rlsb-2 lower leaf regions could be a direct result of reduced RLSB accumulation, since this protein is not present in M cell chloroplasts in any case.
Most interestingly, the rlsb-1/rlsb-2 mutation affected two representative nuclear-encoded proteins as well. The C4 photosynthetic NADP-ME-dependent malic enzyme (NADP-ME, nuclear-encoded, plastid targeted) was significantly reduced (below detectable levels). Similarly, the non-C4 NAD-dependent malic enzyme (NAD-ME, nuclear encoded, targeted to mitochondria) was also greatly reduced (below detectable levels) in lower regions of the rlsb-1/rlsb-2 mutants (Figure 6). In contrast, levels of an RNA binding protein known as CP28 (nuclear-encoded plastid targeted protein [16, 40] were not at all affected in the rlsb-1/rlsb-2 and RLSB/RLSB plants. Similarly, the C4 photosynthetic PEPCase (nuclear encoded, cytoplasmic) was not affected in any region of the rlsb-1/rlsb-2 leaves. The contrasting effects of the rlsb-1/rlsb-2 mutation on two different nuclear-encoded plastid targeted proteins, Cp28 and NADP-ME, is particularly striking. If this were a direct result of reduced RLSB, or an indirect process inhibiting their import/accumulation due to reduced chloroplast function, then both proteins should have been similarly impacted. Similarly, reductions in a plastidic RNA binding protein would not be expected to directly affect the accumulation of a metabolic protein targeted to the mitochondria.
The multiple levels of analysis presented here provide strong evidence that in maize leaves, reduced accumulation of the rbcL mRNA binding protein RLSB leads to corresponding reductions in rbcL mRNA accumulation and LSU synthesis within BS chloroplasts. These findings support a direct effect on post-transcriptional rbcL gene expression, with an impact on both mRNA stability and translation. Indirect effects resulting from reduced RLSB and rbcL expression in the double mutants extend to proteins that are encoded, synthesized, and accumulate within other cell types and other cell compartments.
RLSB localization and basic “default” function in C3plants
RLSB is highly conserved across a broad range of C4 as well as C3 plant species (Additional file 1: Figure S1, Additional file 2: Figure S2). In consideration of this very strong conservation, we hypothesized that RLSB shares a common rbcL regulatory role in all plants, and may have been recruited from a more basic role in C3 species (“default” rbcL regulatory patterns) to function as a cell-specificity determinant in C4 plants (more specialized C4rbcL regulatory patterns). Arabidopsis, with its extensive genetic, molecular biology, and genomic resources (, http://www.arabidopsis.org), provides an ideal model system for comparative RLSB functional analysis in a plant that utilizes the C3 pathway of CO2 assimilation [5–7].
Photosynthesis in C3 plants occurs primarily within leaf mesophyll cells. This general classification of photosynthetic cells makes up the interior of the leaf (between the upper and lower epidermis, excluding vascular cells) and includes the palisade and spongy parenchyma [42, 43]. In leaf sections of Arabidopsis, confocal fluorescent imaging, superimposed on a DIC image, clearly establishes the co-localization of RLSB and LSU proteins within mesophyll cell chloroplasts (Figure 7). A lower magnification overview of similar immunolocalizations indicted that both chloroplast proteins were distributed throughout Arabidopsis leaf mesophyll cell population, with no cell-type preferential or distributional accumulation patterns detected within this population (Additional file 7: Figure S7).
To determine if RLSB is associated with rbcL expression in a C3 plant, a 447 bp inverted repeat fragment of the Arabidopsis RLSB ortholog was expressed and used to induce RLSB silencing in Arabidopsis. Seed from floral-dipped plants were germinated and grown on MS media containing Kanamycin with 3% sucrose. To maintain viability, Kanamycin-resistant plants, which showed very slow growth, were transferred two weeks after germination to MS media containing 8% sucrose without further Kanamycin selection. Six confirmed rlsb-silenced plants were selected for further analysis; all produced nearly identical data. The data sets shown in Figure 8 were obtained from two of these plants that were found by initial protein analysis to have either the least (rlsb-silenced 1) or most severe (rlsb-silenced 2) reductions in LSU accumulation among the six.
Plants expressing the rlsb-silencing construct were easily discernable by their altered morphologies. These included severely reduced shoot growth, altered shoot morphology (there was no typical leaf rosette organization), and purple coloration of the leaves (Figure 8A). The silenced plants did not survive after transfer to soil, and were maintained on the high-sucrose media continuously. The silenced plants rarely produced bolts or flowers, and did not survive longer than 30 days. Seed from control (non-transformed) Col0 plants, germinated and grown using the same 3% and 8% sucrose-media and growth conditions, but without the initial Kanamycin selection, did not show any of these silencing phenotypes (Additional file 4: Figure S4, bottom panels). The size of the rlsb-silenced plants varied between the lines, showing size reductions in overall shoot growth of approximately one-third to one-fourth by 6 to 8 weeks after germination, when compared to Col0 grown on the same media under the same sterile conditions. Root growth on the transgenic plants was also impeded, but to a lesser extent.
Observations of total soluble protein accumulation revealed striking reductions in levels of protein bands corresponding to the Rubisco LSU and SSU in the rlsb-silenced plants (Figure 8B). There were also a few easily observable changes in several unidentified proteins that either increased or decreased in the silenced plants, relative to the controls (Figure 8B). Aside from these, overall patterns of protein accumulation were mostly similar in silenced and wild type Col0 plants. To better understand the levels, range, and specificity of proteins affected by silencing of RLSB, immunoblot analysis was used to check for any possible changes in a range of representative proteins.
Using antisera against LSU and RLSB, dramatic and corresponding reductions in the accumulation both proteins were observed in the rlsb-silenced plants, relative to wild type Col0 (Figure 8C, first and second panels). Levels of LSU protein accumulation varied somewhat between different silenced plants (compare the second and third lanes of Panel 7C), but were always considerably lower than in wild type (25–50 fold for rlsb-silenced 1 and 2, respectively, based on digital imaging analysis). Longer exposures of the immunoblot in the top panel showed that very low levels of LSU protein did in fact accumulate in the silenced plants (Additional file 5: Figure S5, bottom panel). Although RLSB protein was not detected in any of the silenced plants, very low levels of accumulation cannot be ruled out. Detection of this protein by immunoblot required longer exposures even in wild type Arabidopsis (the blot in the second panel of Figure 8C required longer exposure time than the other panels), possibly due to lower steady-state levels of accumulation/stability, or reduced sensitivity of RLSB antibody, relative to LSU.
Analysis of mRNA levels using qRT-PCR indicated that in wild type Col0 plants, rbcL mRNA was considerably more abundant than RLSB mRNA (55-fold more abundant, note the difference in y-axis scales in Figure 8D). Although such dramatic differences in transcript levels may not be reflective of final protein accumulation, the data of Figure 8C and 8D do indicate that the RLSB may be produced or accumulate at lower levels than LSU in plastids of wild type Arabidopsis. In comparing changes in relative levels of rbcL and RLSB transcripts in wild type and rlsb-silenced plants, it is apparent that silencing led to greatly and correspondingly reduced levels of accumulation for both transcripts (Figure 8D). In the silenced plants, both mRNAs showed correlating ratios of reduction, with approximately 25–50 fold lower levels (rlsb-silenced 1 and 2, respectively), relative to wild type for both rbcL and RLSB. The fact that both of these transcripts were detectable, even at greatly reduced levels, indicates that RLSB expression was not completely silenced. The finding that rbcL mRNA and LSU protein levels were reduced in close coordination with levels of silencing for RLSB provides support for our hypothesis that this S1-RNA binding protein affects rbcL gene expression, at least in part, at the levels of translation and mRNA accumulation.
Of four other representative plastid-encoded proteins examined in the rlsb-silenced Arabidopsis, chloroplast coupling factor 1 (CF1αβ alpha and beta subunits) showed an intermediate silencing-associated reduction in accumulation (less than that of LSU, approximately 10 – 12 fold), while PsaC and PsbA levels were mostly unaffected (Figure 8C). As expected, immunoblots confirmed that the nuclear-encoded, plastid targeted SSU was also greatly reduced in the silenced lines; this methodology did not detect any SSU protein in the silenced plants. Another nuclear-encoded, plastid-targeted protein, the Cp28 RNA binding protein [16, 40], was not affected by silencing of RLSB. Two nuclear-encoded cytoplasmic proteins, PEPCase and NAD-dependent malic enzyme (NAD-ME), showed no reductions in the silenced plants (Figure 8C). In fact, NAD-ME showed a slight increase in abundance (approximately 3-fold) relative to control plants.
Taken together, the data shown in Figure 8 indicate that RLSB gene expression was greatly reduced, but not completely eliminated, due to incomplete gene silencing in these Arabidopsis lines. This resulted in a corresponding reduction in levels of rbcL mRNA and LSU protein, providing strong evidence that the nuclear-encoded RLSB protein is necessary for normal levels of rbcL gene expression in the chloroplasts of this C3 plant.
Confirming evidence that RLSB affects rbcL expression was obtained from studies that were initiated using Arabidopsis lines containing a T-DNA insertion within the At1g71720 locus that encodes the RLSB protein in this plant. The data shown in Additional file 8: Figure S8 summarizes findings from one of these lines (SALK_015722, identified through The Arabidopsis Information Resource TAIR and obtained through Arabidopsis Biological Resource Center (ABRC; http://abrc.osu.edu) . The T-DNA insert in this line is within the region encoding the S1 RNA binding domain, which would be expected to eliminate the binding ability and function of this protein. Plants homozygous for the T-DNA insert in this line were never recovered. All of the heterozygote siblings from line SALK_015722 showed reduced accumulation of rbcL-encoded Rubisco LSU protein (Additional file 8: Figure S8A), when compared to Col0 plants, or sibling plants that segregated out the insert (Additional file 8: Figure S8B). Note that in these At1g71720 insertion mutants, levels of LSU were not reduced as dramatically as in the rlsb-silenced plants (approximately 5-fold, as opposed to 25–50 fold in the rlsb-silenced plants). Also unlike the rlsb-silenced Arabidopsis, levels of rbcL mRNA were not reduced in any of these lines (Additional file 8: Figure S8C), suggesting that in this case, translation of rbcL mRNA, but not mRNA stability, was impeded. It should be noted that these lines did not stably maintain the T-DNA insert, so plants heterozygous for the insert in the At1g71720 locus were recovered only rarely, and then not at all after four self-pollinated generations. For this reason, these T-DNA insertion lines were not extensively analyzed, and our focus shifted to the rlsb-silenced lines for the more detailed analyses of RLSB function in Arabidopsis as presented in Figure 8.
The RLSB binding protein in maize and other plants
Findings presented here indicate that RLSB is a nuclear-encoded S1-domain RNA binding protein that interacts with plastid-encoded rbcL mRNA, thereby activating or enhancing rbcL gene expression. RLSB was purified from chloroplasts based on its specific binding to the 5’ region of rbcL mRNA in vitro. The purified protein is highly conserved among a wide variety of monocot and dicot C3 and C4 plant species, and contains a predicted plastid transit sequence. It is localized to chloroplasts in both the C3 dicot Arabidopsis and the C4 monocot maize. Most significantly, in the leaves of all three C4 species examined, it co-localized with Rubisco only within BS cell chloroplasts, corresponding with the specific cellular compartmentalization of Rubisco in C4 leaves.
RLSB is an S1 binding domain protein in the same category as the ribosomal protein S1, from which this class is named . Other than its conserved binding domain, RLSB is a unique chloroplast protein; it shows very little overall identity with known examples of plastidic ribosomal S1 proteins, including those from spinach (AAA34045.1), cucumber (ABK55725.1), rice (ABF95618.1) or Chlamydomonas (CAE51165.1). Stretches of amino acids spanning the S1 RNA binding domain display 33% - 73% maximum identity with gaps, depending on the species comparisons. However, outside of this conserved domain there are no extensive regions of significant similarity between the plastidic RLSB and ribosomal S1 proteins. RLSB orthologs in Arabidopsis, maize, and other plant species used for our comparisons (Additional file 1: Figure S1, Additional file 2: Figure S2) appear to be unique members of the S1 class of RNA binding proteins, distinct from other known proteins of this class, and from other known plastidic RNA binding proteins.
The S1 binding domain that distinguishes this protein is found in a large number of RNA binding proteins . The S1 binding domain structure is very similar to that of cold shock proteins, and appears to be derived from a very ancient class of nucleic acid binding proteins. While these proteins are known to be widespread among a variety of organisms, there is very little known about the function of proteins that contain this domain. In higher plants, some non-ribosomal proteins known to possess S1 domains include the plastidic polynucleotide phosphorylase , RNase E/G-type endoribonuclease , and exosome subunit AtRrp4p . Examples of other known S1-domain proteins include transcription factor NusA and polynucleotide phosphorylase in bacteria [48, 49], and a nucleic acid binding protein of unknown function in humans .
Analysis by immunolocalization as well as mechanical cell-separation demonstrated the BS-specific localization of RLSB in leaves of the C4 plant maize. Maize proteomic data localizes RLSB to the chloroplast nucleoid, where transcription is coupled to post-transcriptional RNA processing and translation ; http://ppdb.tc.cornell.edu/dbsearch/gene.aspx?id=674610. This is a very comprehensive database, however it does not provide information about the occurrence of RLSB in separated BS or M cells. This information is provided for other C4 proteins (for example, see Rubisco LSU, http://ppdb.tc.cornell.edu/dbsearch/gene.aspx?id=652357). Protocols for separating BS and M cells have been shown to affect the accumulation of some BS and M proteins in C4 plants (for example, ), and it is possible that RLSB was not present when the separated BS and M extracts were used for proteomic analysis. The absence of RLSB from the separated cell populations might be related to our observation that this protein does not appear to be stable in the disrupted BS cells after separation by leaf rolling. This is why the BS-enriched strands were used immediately for protein isolation, without further purification of the BS strands after the M cell “roll out” (Figure 2).
This current study is focused on RLSB protein, and not its mRNA. Still, it is important to mention that our experimental findings of BS specificity for RLSB protein in maize might not appear to be in agreement with data contained in two recent maize transcriptome databases (30, 33), which have analyzed mRNA populations in separated BS and M cells. For example, using the B73 C3/C4 transcriptome web browser tool (http://c3c4.tc.cornell.edu/search.aspx) of Li et al.  for RLSB (GRMZM2G087628) mRNA, only a portion of the transcript sequence is indicated as being present in both the laser capture microdissection (LCM) leaf tip (mesophyll) and LCM leaf tip (bundle sheath) graphs from that database. The first four exon sequences from the 5′ portion (more than half of the full-length mRNA sequence) are missing from these two graphs; only 3′ exon sequences are indicated as being present in the two separated cell types. This might imply an anomaly for RLSB mRNA in the separated cell populations. In contrast, transcriptome graphs from leaf tip and leaf base (cells not LCM separated, combined transcripts from both cell types) show all eight exon sequences present. In stronger contradiction to our RLSB protein data, the transcriptome database of Chang et al.  (based on enzymatic digestion-mechanical separation instead of LCM) actually indicates that GRMZM2G087628 transcript sequences are significantly more abundant in M cells than in BS cells (>13 fold). These databases are both very comprehensive and useful tools for analysis of C4 gene expression. However, for reasons stated above, it is possible that the integrity/cell specificity for this particular mRNA was not maintained during the cell separation protocols utilized for those databases, leading to conflicting findings. Alternatively, post-transcriptional control of RLSB mRNA processing, stability, or translation could be involved in determining cell-type specificity for the RLSB protein, as has been found for genes encoding Rubisco and many other C4 proteins [5–7, 11]. An analysis of RLSB mRNA transcription, accumulation, and stability in BS and M cells is currently under investigation and will be included in a separate study.
In Arabidopsis, the eFP browser (http://bbc.botany.utoronto.ca/efp/cgi-bin/efpWeb.cgi) shows a strong correlation in the timing of expression of mRNA accumulation, primarily in photosynthetic (green) plant tissues, for RLSB (At1g71720) (http://www.bar.utoronto.ca/efp/cgi-bin/efpWeb.cgi?dataSource=Developmental_Map&modeInput=Absolute&primaryGene=At1g71720%20&secondaryGene=None&modeMask_low=None&modeMask_stddev=None) and rbcL (Atcg00490) (http://www.bar.utoronto.ca/efp/cgi-bin/efpWeb.cgi?dataSource=Developmental_Map&modeInput=Absolute&primaryGene=Atcg00490%20&secondaryGene=None&modeMask_low=None&modeMask_stddev=None), providing additional correlative evidence for RLSB and rbcL interaction. The online expression profiles indicate that in Arabidopsis, an exception to the RLSB and rbcL correlation occurs in dry seed, where transcripts for RLSB, but not rbcL, occur in abundant amounts. Rubisco mRNAs and enzymatic activity have been found to occur transiently during very early seed development, dropping off at later stages [53, 54]. During seed development in Brassica napus, Rubisco activity, independent of the calvin cycle, has been shown to enhance carbon acquisition, which promotes the formation of seed oil . In addition, mRNA accumulation and translation of the LSU and SSU proteins can occur very soon after germination [5, 8, 56–58]. Thus, there is a potential role for RLSB during seed development, and possibly for enabling the rapid onset of early Rubisco synthesis during germination.
RLSB binding activity, and rbcL gene expression in maize and Arabidopsis
RLSB was isolated based on its ability to bind rbcL 5′ RNA but not a control RNA in vitro, indicating at least some specificity for the Rubisco chloroplast transcript. Further analysis by RIP/qRT-PCR extended these initial findings by demonstrating prominent selective binding of RLSB to rbcL mRNA, but not other plastid-encoded transcripts, in vivo. The in vivo assay also revealed the possibility of much weaker interactions with psbA, atpA, and atpB mRNAs, all of which accumulate in both BS and M plastids of maize leaves, with psbA actually being far more abundant in M plastids [39, 59]. The fact that RLSB was not detectable in maize M cells would suggest that this greatly reduced binding activity to mRNAs other than rbcL might not be biologically significant, likely caused by background binding within the chloroplast lysates. The data presented here cannot rule out the possibility that RLSB may in fact have additional target RNAs within BS chloroplasts that were not identified because they were not included in this assay. Higher plant chloroplast genomes can encode over two hundred protein-encoding and non-coding mRNAs [6, 60, 61]. A genomics-based search for additional mRNA targets in maize and Arabidopsis plastids is required to definitively identify the full range of RLSB binding specificity, and is currently in progress. However, the finding that RLSB interacted preferentially with rbcL mRNA, and only weakly or not at all with any of the other six plastid-encoded mRNAs examined, indicates a very high degree of binding selectivity.
In maize, the developmentally early lower regions of rlsb-1/rlsb-2 leaves displayed greatly lowered RLSB protein accumulation, together with reductions in levels of rbcL mRNA, as well as in the accumulation and synthesis of the LSU protein. All of these mutation-associated changes (rbcL mRNA, LSU accumulation and synthesis) correlated very closely in these same lower leaf regions. These parameters all recovered to normal non-mutant levels in the developmentally advanced outer regions. Thus, in maize rlsb-1/rlsb-2 mutants, RLSB production, and associated LSU synthesis/accumulation, were delayed (but not eliminated) along the maize leaf developmental gradient. In comparison, rlsb-silencing in the C3Arabidopsis plant led to greatly reduced levels of RLSB mRNA and its encoded protein throughout the entire length of the leaf, relative to wild type Col0. Throughout the same silenced leaves, strongly correlating reductions in rbcL mRNA and LSU protein also occurred.
When comparing the effects of reduced RLSB expression in the silenced Arabidopsis and transposon-mutagenized maize, some similarities and significant differences become apparent. In both the C3 and the C4 experimental plant systems, reductions in levels of RLSB and rbcL mRNA, as well as their encoded proteins, occurred in approximate coordination (Figures 5 and 8). Such findings support a common regulatory connection between RLSB and levels of rbcL gene expression in both plants. As in RLSB/RLSB maize, Col0 Arabidopsis leaves had more abundant levels of rbcL mRNA than RSLB mRNA (Figures 5B and 8D, note the difference Y-axis scales). However, in Arabidopsis this difference was less pronounced (25–50 fold, relative to more than 150-fold in maize). In maize, insertion mutagenesis did not completely eliminate RLSB expression, allowing for reduced but detectable levels of rbcL expression in lower rlsb-1/rlsb-2 leaf regions. Silencing of RLSB in Arabidopsis resulted in much more dramatic effects than in the maize mutants, but very low levels of RLSB and rbcL expression were still detectable in these plants.
Lowered RLSB expression in both plants led to corresponding coordinated effects on levels of rbcL mRNA accumulation, LSU synthesis (in maize), and LSU accumulation. Lowered levels of rbcL mRNA in RLSB-silenced Arabidopsis and rlsb-1/rlsb-2 maize mutants suggest that RLSB is required for the stabilization of these transcripts. However, the finding that LSU synthesis and accumulation were reduced much more dramatically than rbcL mRNA in rlsb-1/rlsb-2 lower leaf regions (approximately 4-fold for mRNA, 15 fold for protein), and reduced LSU accumulation was not accompanied by lower rbcL mRNA in the Arabidopsis At1g71720-insertion heterozygotes, suggests a role in translation as well. Similar to the data of Figure 5B, an earlier study also found that rbcL mRNA accumulation in maize was reduced approximately four-fold in response to a decrease in translation . In fact, many studies have confirmed a close relationship between the processes of transcript stabilization and translation in chloroplasts, with both processes regulated by RNA binding proteins [5, 16, 17, 24, 62]. Taken together with the in vitro and in vivo binding data, evidence presented here clearly implicate RLSB as a key determinant of rbcL gene expression in the chloroplasts of all photosynthetic leaf types in C3Arabidopsis, and exclusively in the BS chloroplasts of C4 maize. The tight correlative changes associated with lowered RLSB expression (confirmed by multiple levels of analysis) are strongly indicative of a regulatory link between RLSB and rbcL gene expression, with RNA binding possibly implementing an effect at the level of RNA metabolism (rbcL mRNA translation and stability).
A significant difference between the two plant systems was apparent when comparing the effects of reduced RLSB on proteins other than LSU (Figures 6 and 8E). Although there were no effects on nuclear-encoded PEPCase or CP28 in either plant, effects on other representative plastid- and nuclear-encoded proteins differed considerably. In contrast to maize, reduced RLSB in Arabidopsis was not associated with any changes in the accumulation of the plastid-encoded PsaC or PsbA (components of PSI and PSII, respectively), while reductions in CF1αβ were considerably less pronounced. The nuclear-encoded NAD-ME actually increased in the rlbs-silenced Arabidopsis, as opposed to the strong decrease observed in the maize mutants. It might be expected that any direct effects of reducing this highly conserved S1 binding protein would be consistent between the C3 and C4 plants, with shared reductions in LSU being distinctly prominent. However, with regards to effects on other proteins, variations between two photosynthetic systems proteins were clearly evident.
Other effects of reduced RLSBexpression
In maize, reduced and delayed RLSB and LSU production in rlsb-1/rlsb-2 lower leaf regions was associated with strong decreases in the accumulation of several additional plastid- and nuclear-encoded proteins. Reductions in levels of the nuclear-encoded SSU protein were expected, since the expression, synthesis, and assembly of the two Rubisco subunits are tightly coordinated [7, 20, 63]. It was, however, surprising to observe such strong reductions in other representative plastid- and nuclear-encoded proteins. Like LSU, these all increased to normal levels in outer regions of the leaf. Developmental increases in rbcL and RLSB expression were also associated with basipetal recovery of the virescent phenotype in rlsb-1/rlsb-2 leaves. Multiple effects similar to those in the rlsb-1/rlsb-2 mutants have been associated with other maize mutations that affect general regulators of plastidic gene expression, such as cps and hcf. However, there are several characteristics and observations that distinguish the rlsb mutants from the general regulator mutants. First and most importantly, findings presented here clearly demonstrate that RLSB is strictly confined to chloroplasts within the maize leaf BS cells. However, most of the affected plastid-encoded proteins actually accumulate equally, or even more abundantly, within M cell chloroplasts of wild type maize leaves [39, 59]. A general regulator that is specifically localized within BS chloroplasts could not directly affect translation of mRNAs in M chloroplasts. Second, while severe reductions in PsaC and PsbA were associated with decreased RLSB expression and LSU production in the lower leaf regions of rlsb-1/rlsb-2 maize mutants, these same proteins were not affected at all in the rlsb-silenced Arabidopsis, even in the presence of much more severe RLSB and LSU decreases. A highly conserved general regulator of ribosome assembly would be expected to have the same function and produce analogous effects in both plants. Third, there was no significant decrease in plastid ribosomal RNA levels observed for the rlsb-1/rlsb-2 mutants, indicating that, unlike the cps and hcf mutants, ribosome accumulation was not affected. Fourth, in contrast to the cps and hcf mutants that affect only translation, the rlsb-1/rlsb-2 mutants showed variation in accumulation levels for several plastid mRNAs as well. Fifth, unlike the general plastidic regulators, the effects of rlsb-1/rlsb-2 mutants were not confined to the chloroplasts; levels of two nuclear-encoded proteins were also significantly reduced, including the NADP-ME that was not affected in cps or hcf mutants . It is clear that RLSB shows selective binding to rbcL mRNA in affinity purification and in RIP/qRT-PCR analysis; binding to other plastid-encoded transcripts, including those with severely reduced protein accumulation in lower rlsb-1/rlsb-2 leaf regions, was minimal or did not occur. These distinguishing characteristics, together with the BS-specific localization of RLSB, its selective binding to rbcL mRNA and clear effects on LSU production, confirm the distinct identity of this protein, functionally separating it from the previously identified plastid ribosome assembly mutants of maize.
All of the recovered rlsb-silenced Arabidopsis had multiple developmental abnormalities, including dark purple leaves, reduced leaf size, and impaired root development. They did not produce bolts or flowers, and died after 30 days. These effects were not observed on non-transformed plants grown without selection on the same medium under the same conditions (Additional file 4: Figure S4, bottom panels). These effects were also not observed in any of the heterozygous At1g71720-insertion plants, which showed much less severe reductions in LSU accumulation. While anthocyanin production is known to increase when Arabidopsis plants are grown in the presence of high sucrose [64, 65], leaves of the rlsb-silenced plants had much darker pigmentation than leaves of non-transformed plants grown on the same high-sucrose media. The very high levels of purple pigmentation is an indicator of a stress response . It is clear that in this C3 plant species, severely lowered levels of RLSB not only leads to greatly reduced production and accumulation of Rubisco, but also affects many other aspects of growth and development.
The more severe reduction in RSLB expression in rlsb-silenced Arabidopsis correlated with a much greater effect on LSU mRNA and protein accumulation than in rlsb-1/rlsb-2 maize leaves. Based on the sampling of proteins shown in Figure 8, it appears that the greatly reduced RLSB expression did not result in a strong general cessation/decrease of proteins other than LSU and its associated SSU in this C3 plant. Like increased anthocyanin, increases in the nuclear-encoded mitochondrial enzyme NAD-ME are often occur in response to plant stress [5, 66, 67], in this case possibly brought about by growth/developmental challenges in the silenced Arabidopsis.
Several studies have also demonstrated that plants with reduced Rubisco are recoverable and viable [63, 68–72]. In some cases these plants can have their growth enhanced by supplementing atmospheric CO2, or for the rlsb-silenced Arabidopsis described here, by adding additional carbon source to the media to facilitate more heterotrophic growth. In contrast to the multiple associated effects reported here for the rlsb-1/rlsb-2 mutants, a recent study with a different maize mutant showed that greatly reduced Rubisco accumulation, caused by a defect in the assembly factor RAF1, did not show any effects on other plastid-encoded proteins . It may be important to consider that separate analysis of lower and upper leaf regions were not reported in that study, and the developmental stages analyzed might not be directly comparable to those used here. However, the finding that greatly reduced Rubisco within the raf1 mutant leaves had no observable effect on any other plastid-encoded proteins represents a clear difference from the effects observed in lower regions of the rlsb-1/rlsb-2 leaves. It could be relevant that RLSB impacts the earliest step of LSU synthesis, whereas RAF1 affects Rubisco accumulation at the much later step of Rubisco assembly/degradation.
At this stage, we can only speculate about mechanisms by which reduced RLSB expression in maize would have such a dramatic effect on the production of several plastid- and nuclear-encoded proteins other than LSU and SSU, especially with regards to genes not encoded within BS chloroplasts. A broad-range coordinated impact on multiple photosynthetic genes is certainly not unique to the rlsb-1/rlsb-2 effects presented here. Numerous studies have demonstrated that photosynthetic metabolism affects plastid gene expression at the levels of transcription, translation, as well as assembly/stabilization of PSI, PSII and PET complexes [6, 17, 73, 74]; many photosynthesis-associated nuclear genes are affected as well [6, 73–76]. A few notable examples of widespread regulation of photosynthetic genes, mediated through transcriptional or post-transcriptional regulation, occur during high light stress , photomorphogeneis , and stress-induced mRNA decay . Photosynthetic signaling-regulatory networks occur within and outside of chloroplasts, involving close interactions between cells and different cellular compartments. These networks extend to mitochondria, where NAD-ME is localized [75, 80–82]. Lower levels of Rubisco and the resulting impact on carbon fixation would redirect photosynthetic electron transfer, leading to the generation of redox signals such as reactive oxygen species, hydrogen peroxide (H2O2) and O2 itself [73, 74, 77, 83, 84]. Other processes known to regulate photosynthetic genes, such as the rate of CO2 fixation, carbon metabolism, photosynthetic intermediates, and sucrose accumulation [5, 6, 80, 82, 85, 86] could all be impacted by reduced Rubisco production in rlsb-1/rlsb-2 maize mutants and rlsb-silenced Arabidopsis. In consideration of these effectors, it is perhaps not too surprising that inhibition of LSU synthesis early in the development of the C4 maize leaf might signal suppressive effects on the expression of other genes related to photosynthetic function or metabolism, even in other cell types and cellular compartments. Affected genes in the rlsb-1/rlsb-2 mutants include redox and sink-responsive light-reaction genes in BS and M cells, the nuclear-encoded plastid-targeted decarboxylating NADP-ME in BS cells, and the mitochondrial NAD-ME. While little is known about the regulation of metabolic (non-photosynthetic) NAD-ME in NADP-ME-type C4 plants such as maize , it is clear that this protein, which is encoded, translated, and functions outside of the chloroplasts, was also greatly reduced in the rlsb-1/rlsb-2 mutants. Also unclear is why associated effects on some proteins were severe in the C4 leaves of maize, but for the most part did not occur in the C3 leaves of Arabidopsis. Differences in the severity of RLSB-associated effects in maize and Arabidopsis could be related to the more complex, multi-compartmental regulatory interactions required for energy-intensive C4 differentiation, abundant gene expression/protein accumulation, and enhanced photosynthetic capacity [5, 11, 82].
For all of the experiments described above, we never recovered any rlsb-silenced lines of Arabidopsis, homozygous Arabidopsis At1g71720 T-DNA insertion mutants, or any rlsb-1/rlsb-2 maize lines, in which RLSB or LSU had been completely eliminated. Incomplete silencing, heterozygosity, and partial suppression of mutator activity all appear to have allowed for low levels of RLSB expression in each of the experimental systems used here. We expect that complete absence of RLSB would result in a complete absence of LSU production, severely reducing seed or seedling viability.
The progressive base to tip variation in phenotype (virescent to green phenotype, increases in synthesis and accumulation of LSU and other proteins) observed in rlsb-1/rlsb-2 leaves is not unique. A recovery to wild type phenotype also occurred at the leaf tip of the transposon-based bundle sheath defective (bsd1, an ortholog of G2) maize mutants . It is likely that the much lower levels RLSB and LSU produced within rlsb-1/rlsb-2 lower leaf regions, relative to the same region of RLSB/RLSB leaves, caused a delay but not a cessation of full photosynthetic development for these leaves. Significantly lowered production would be expected to cause a slower buildup of both proteins in the less advanced lower region, relative to the much more rapid accumulation that would normally occur in the same region of wild type leaves. In this scenario, reduced RLSB and LSU production would slow their rates of accumulation along the length of the maize leaf developmental gradient. Eventually, levels of accumulation would “catch up” to normal RLSB/RLSB levels, but much further up along the developmental gradient. The more gradual increase along the length of the gradient would eventually allow both protein to reach wild type levels, but only in the older developmentally advanced upper regions of rlsb-1/rlsb-2 maize leaves.
It is known that transposon insertion within a gene does not always lead to the complete elimination of the gene’s activity . In the case of Mu, there are several potential causes for partial suppression of mutator activity. Although somatic excision could lead to recovery of expression , there was no detectable excision from the RLSB gene at the leaf base, or more significantly, at the leaf tip (not shown). There are also potential epigenetic effects from insertions near promoters or introns [88–90]. Both the rlsb-1 and rlsb-2 insertions were within the first exon, 8 and 45 nucleotides, respectively, of the first 5’ splice junction. This localization presents a likely mechanism, which is the use of an in-frame 5’ donor site within the Mu transposon. Use of the Mu donor site can cause alternative splicing [88, 89, 91]. In this case, removal of transposon sequence from some rlsb-1 or rlsb-2 transcripts might have caused minor changes (such as a small deletion) within mRNA sequences encoding the RLSB N-terminal region, leading to reduce production, accumulation, and/or functionality. Additional studies will be required to determine exactly how these Mu insertions affect RLSB function in these mutant plants.
To understand the elusive molecular processes that mediate BS or MP cell-specific gene expression in C4 plants, and how such processes might have developed from pre-existing C3 forms, it is essential that gene-specific trans-acting regulatory factors with properties unique to this photosynthetic pathway be identified [5, 7, 11, 12]. In C4 leaves, such factors would be expected to show localization or activity that is specific to only one of the two specialized photosynthetic leaf cell-types. It is likely any trans-acting factors responsible for the highly specific C4 expression patterns would not have originated de-novo, but would actually occur and be functionally present in a “default” expression mode in C3 plants [5, 7, 11]. The modification of RLSB binding activity to BS cell-specificity in C4 plants would not require any changes to the rbcL gene itself. In fact, regulatory regions of these plastidic genes are highly conserved across C3 and C4 plant species . The strict correlation between RLSB and rbcL gene expression, occurring at several levels as determined by multiple levels of analysis, suggests that BS-specific accumulation of the RLSB binding protein to rbcL mRNA may be one determinant leading to the BS-specific localization of Rubisco that is characteristic of kranz-type C4 plants.
The mechanism(s) by which RLSB post-transcriptionally activates or enhances rbcL gene expression in C3 and C4 plants is under investigation. Plastidic mRNA binding proteins often function in association with other proteins; in fact, the rbcL mRNA-based affinity purification of several proteins along with RLSB provides evidence that this protein may function as part of a larger protein complex. How this and any associated proteins had their expression modified to become BS specific during the evolution of C4 capability will involve “going back a step” from our traditional levels of analysis, focusing on the cell-type specific regulatory gene (RLSB), instead of the cell-type specific gene (rbcL) at the end of a proposed and possibly extensive regulatory chain. Previous studies of C4 gene expression have revealed a complex regulatory system, involving multiple levels of transcriptional, post-transcriptional, and post-translational control, all integrated together to achieve full C4 photosynthetic capacity. There is no evidence for a “global regulator” of C4 expression; genes encoding different photosynthetic enzymes show unique patterns of expression indicative of independent regulation . RLSB, as a regulator of rbcL gene expression, provides a new insight into how one component of this extensive photosynthetic regulatory system might have been modified from an original C3 “default” function to perform the same function, but in a more specialized fashion, in C4 plants.
RLSB was isolated from chloroplasts of a C4 plant by affinity-purification based on its ability to bind rbcL mRNA in vitro. This protein, encoded by the nuclear RLSB gene, contains an S1 nucleic acid binding domain and is highly conserved among a wide variety of C4 and C3 plant species. RLSB contains a plastid transit sequence, and co-localizes with LSU to chloroplasts. Most significantly, it accumulates specifically within the BS chloroplasts of maize and other C4 plants. In maize chloroplasts, RLSB showed selective binding to rbcL mRNA, but not to other representative plastid-encoded transcripts. In maize RLSB insertion mutants, RLSB accumulation was reduced along the leaf developmental gradient, with lowest levels at the leaf base, and increasing levels toward the leaf apex. Delayed/reduced RLSB accumulation led to corresponding reductions in rbcL mRNA accumulation as well as synthesis/accumulation of LSU protein, indicating regulatory functions at the levels of mRNA stability and translation. Other developmental effects included virescent/yellow leaves and reductions in several additional proteins (including some PSI and PSII components) that locate to other cellular compartments and cell types of C4 leaves. Effects such as these were likely associated with decreased photosynthetic function and disruption of associated signaling networks. Reduction of RLSB production in Arabidopsis by RNA silencing or insertion mutation revealed that, as in C4 maize, RLSB affects rbcL gene expression at the levels of mRNA and protein accumulation in the chloroplasts of this C3 plant. While reduced RLSB in both maize and Arabidopsis lead to corresponding decreases in rbcL mRNA and LSU protein, secondary effects (reductions for other proteins) in Arabidopsis were not as severe as in maize. The strict co-localization to Rubisco containing chloroplast and tight correlation with rbcL gene expression suggests RLSB may play an essential role in determining photosynthetic gene expression in all plants, and possibly contribute to BS-specific localization of Rubisco in C4 plants.
Plant material and growth conditions
Amaranthus hypochondriacus var RI03, Flaveria bidentis, Setaria viridis, and Arabidopsis plants were grown in artificial soil in a greenhouse, or in a growth chamber in soil or on media (see below) using growth conditions described previously [56, 67, 93]. Maize (Zea mays) lines containing the rlsb-insertion (rlsb-1/rlsb-2, rlsb-1/+ and rlsb-2/+), and sibling lines lacking the rlsb Mu insert (RLSB/RLSB), as well as wild type maize line B73  were grown in artificial soil in a growth chamber (14 h/d illumination at 170–200 mmol photons m-2 s-1, with 22°C day 19°C night temps).
RNA affinity purification of RLSB protein from chloroplasts extracts
Extracts for RNA binding were prepared from purified amaranth chloroplasts as described . Extracts used for purification were approximately 1 – 2 mg protein per ml, as determined using a Bradford protein assay (Bio-Rad).
In vitro transcriptions and acrylamide gel purification of RNAs corresponding to the 5′ region of the amaranth rbcL mRNA (beginning at the −66 processed end of mature rbcL transcript, and ending at the +60 position) and control 7z-AS RNA (a 130 nt 3’ UTR from a yeast viral RNA ), were performed using DNA templates and methods described previously . The rbcL 5’ and control RNA was labeled with biotin at its 3’ end using Biotin hydrozide (EZ link Biotin-LC-hydrozide, Thermo Scientific) according to manufactures protocols (http://piercenet.com/instructions/2160124.pdf). The 3′-biotinylated RNA was ethanol precipitated twice, resuspended in RNAse-free H2O, and stored at −80°C.
For each RNA affinity purification, 50 μl of streptavidin magnetic beads (New England Biolabs) were used. Beads were separated from supernatants using a magnetic stand (New England Biolabs). The beads were first washed twice with binding buffer (40 mM KCl, 10 mM MgCl2, 3 mM dithiothreitol, 0.05 mM EDTA, 8.5% (v/v) glycerol, 10 mM HEPES, pH 7.9, and at least 0.5 mg/μl of tRNA as a nonspecific competitor), and then incubated with either 2 ml biotinylated 5′rbcL or biotinylated 7z-AS RNA (approximatey 25 picomoles per ml) for 10 minutes. The RNA coated beads were then washed twice with binding buffer.
Extracts for binding reactions were adjusted to 1X binding buffer and 0.5 μg/μl tRNA, and pretreated with buffer-washed beads (200 μl of plastid extract to 50 μl beads) prior to use in binding reactions (beads used for this pretreatment were discarded). Pre-treated extract (80 μl) was then added to each 50 μl aliquot of RNA coated beads, and the binding reactions were incubated at room temperature for 15 minutes. The beads were then washed twice with binding buffer. Washed beads were treated with 2 μl of RNAse cocktail (Ambion) for 15 minutes at room temperature, and loaded onto a 22 cm long 10% SDS-PAGE gel. Bands of interest visualized by silver staining were cut from the gel and subjected to trypsin digestion and Maldi-Tof mass spectrometry (Custom Biologics, Toronto, CA).
Antisera against conserved peptide sequences within the Arabidopsis RLSB protein were produced in rabbits using the peptide sequences shown in Figure 1C (Proteintech Group, Inc., Chicago, IL, http://www.ptglab.com). This antisera was affinity purified using the 149 aa peptide that is shown in Figure 1C, using an UltraLink iodoacetyl micropeptide coupling kit (Thermo Scientific). The 149 aa peptide itself, containing a T7 tag, was expressed in E. coli using the pET-17b expression vector, and purified using a T7∙Tag Affinity Purification kit (Novagen).
Antibodies against the Rubisco large subunit (LSU), PEPCase, and NAD-ME have been described [66, 94, 95]. Antisera against the plastid proteins PsaB, PsaC, PsbA, and AtpB were obtained from Agrisera (Vännäs, Sweden, http://www.agrisera.com). Antisera against Cp28, CF1αβ (this antisera reacts to both the alpha and beta subunits), and NADP-ME were the generous gifts of Masahiro Sugiura (Nagoya University, Nagoya Japan), Julian Hibbard (University of Cambridge, UK), and Richard Leegood (University of Sheffield, UK), respectively.
Immunolocalizations were performed using paraffin-embedded leaf sections, as described [94, 95]. Arabidopsis leaf sections were taken from fully expanded leaves of Col0 plants, midway between the apex and base. Leaf sections of maize line B73 were taken from first or second 10 – 14 cm long leaves, approximately midway between the apex and the base. Sections from Flaveria bidentis, Setaria viridis, and Arabidopsis plants were taken from young leaves between one third to one half full expansion, approximately midway between the apex and base. Sections were reacted with the primary antisera indicated in the Figures, and then secondary antisera conjugated with R-phycoerythrin or Alexafluor 546 (Molecular Probes/Life Technologies, Carlsbad, California). Epifluorescence images were captured using a DM IRE2 inverted compound microscope (Leica Microsystems, Wetzlar, Germany) equipped with fluorescent and brightfield imaging systems, and a Retiga Exi cooled CCD camera (Q Imaging, Burnaby, BC, CA). Confocal images were captured using an LSM710-InTune Confocal (inverted) Microscope System with Zen Imaging software (Carl Zeiss MicroImaging), using a 20X or 40X objective; Alexafluor 546 excitation was done using a 529 nm laser line, and fluorescence was collected at 564–577 nm.
Silencing of RLSB in Arabidopsis
Primers corresponding to a 447-nt region of the Arabidopsis RLSB ortholog (Figure 1, Additional file 9, accession #JX843767) (a region unique to RLSB to eliminate off-target silencing) was inserted as an inverted repeat into the pHannibal silencing vector, and then mobilized into the pART27 binary vector . Six-week-old Arabidopsis Col-0 plants were transformed using floral dip . Agrobacterium treated seeds were surface-sterilized using vapor-phase sterilization, and germinated on solid MS medium with 3% sucrose. Germination and the first 14 d of growth occurred under 16-h illumination at 22°C in Petri dishes containing kanamycin (100 mg/L), after which resistant seedlings were transferred to and sterilely maintained in PlantCon tissue culture containers (MP Biomedicals) on MS medium with 8% sucrose, without selection. Potential rlsb-silenced lines were harvested and assessed (using PCR to check for correct inserts and qRT-PCR to confirm reduced RLSB mRNA levels) at 6–8 weeks. Six of the confirmed rlsb-silenced plants were selected for further analysis; data from two of these plants (designated rlsb-silenced 1 and 2) are shown in Figure 8, panel D. As controls, non-transformed seed from wild type Col0 plants were germinated and grown, and transferred using the same media and growth conditions, except without initial Kanamycin selection (Additional file 4: Figure S4, bottom panels).
Mutant maize lines
Mu insertions in the maize RLSB gene (rlbs1 and rlbs2) were identified in a maize line with active Mutator (Mu) transposons by screening with oligonucleotides based on the maize ortholog of RLSB (accession #JX650053) and both borders of the Mu insert (Additional file 3: Figure S3 and Additional file 9). The mutation is inherited as a single, recessive Mendelian trait. It’s effects were visualized in seedlings with virescent 1st, 2nd, and 3rd leaves, which gradually green starting at the tip and progressing in the basepetal direction (Additional file 4: Figure S4, top panels). No virescence was observed in wild type plants grown under the same conditions. Unless noted, leaf material from the mutant plants was isolated from 6 – 8 cm 2nd or 3rd leaves.
Protein accumulation and synthesis
Soluble or membrane-bound protein extracts were prepared as described [57, 67, 95]. Total maize leaf protein extracts were prepared according to the methods of . A mechanically separated and purified population of M cell, and a population of BS/m (BS enriched) cells, were prepared from 15 cm third leaves of maize B73 using the leaf rolling method of ; soluble proteins were extracted from each population. For each experiment, equal amounts of protein were loaded into lanes of an SDS-PAGE gel, electrophoresed, and either silver-stained or transferred to Protran nitrocellulose (Whatman) or Immobilon polyvinylidene fluoride (PVDF) membranes (EMD Millipore) for immunoblotting. Antibody reactions were detected using an ABC luminol reagent system (Amersham), and visualized using a Storm phosphorimager and ImageQuant software (GE Healthcare).
In vivo protein synthesis was determined by radioactively labeling 10 mm maize leaf disks placed into a solution containing 100 μCi of [35S]Met/Cys express labeling mix (PerkinElmer NEN Radiochemicals) in 400 μL of water. After one hour, proteins were extracted from equal wet weight of material. Tricarboxylic acid (TCA) precipitation of proteins from each extract , together with equal amounts (wet weight) of starting leaf material, confirmed equalized loading of samples. Protein extracts were used directly for analysis of total protein synthesis by SDS-PAGE, or immunoprecipitated from equal amounts of labeled protein extracts as described [56, 95].
RNA isolation and real-time quantitative PCR
RNA was isolated from Arabidopsis and maize leaves using an RNeasy Plant Mini Kit (Qiagen) according to manufactures protocols. cDNA synthesis was performed using an iScript cDNA synthesis kit (Bio-Rad) using oligo(dT) and random primers included in the kit. Real time quantative PCR (qRT-PCR) was performed using SYBR Green Supermix (Bio-Rad) on a MyiQ™2 Two Color Real-Time PCR Detection System (Bio-Rad), using primers for plastid- or nuclear-encoded mRNAs (Additional file 9) as indicated in the Figures. Quantitative expression data was normalized to Arabidopsis or maize actin, rpl2, rpl20 or rps3, as indicated in the Figures. Relative quantification in expression of the target gene relative to that of a control transcript was measured by using the 2-ΔΔCt calculations. Statistical significance was calculated using Student’s T-test. For each bar shown in the graphs, P values were less than 0.05.
RNA immunopurification with real-time quantitative PCR
Extracts for RIP/qRT-PCR were prepared from purified maize chloroplasts (containing both BS and MP plastids) as described  (http://pml.uoregon.edu/RIP-chip%20Protocol.pdf). 1 ml aliquots from one prepared lysate were used for each of the three immunopurification reactions described below. Each aliquot was first cleared by centrifugation at 12,000 rpm, then treated with 100 μl of Staph A cells (Pansorbin, Calbiochem), washed with CoIP buffer (20 mM Tris–HCl, pH 7.5, 150 mM NaCl 1 mM EDTA0.5% NP-405 μg/ml aprotinin for 10 minutes on ice. Three pretreated lysate aliquots were used for three types of IP reactions, using antisera against RLSB, and as controls, PEPCase and a mock reaction with no added antibody. The lysates were incubated with 15 μl of antibody (or control buffer) with rotation at 4°C overnight. The antigen-antibody complexes, and the no-antibody control reaction, were precipitated using 100 μl Staph A cells pre-treated and washed as described . RNPs were disrupted by adding 25 μl 10% SDS and 10 μl 200 mM EDTA to 225 μl of the final re-suspension. 1 μl GlycoBlue (Ambion) was added to aid in recovery and visualization of small amounts of RNA. RNAs were extracted from disrupted pellets and supernatants using phenol-chloroform-isoamyl alcohol, and ethanol precipitated. The purified RNA samples were used for qRT-PCR as described above with primers for the maize chloroplast-encoded mRNAs (Additional file 9) as indicated in Figure 3, and Additional file 6: Figure S6. All data shown represent at least two repeat reactions of three independent experiments.
Large subunit of Rubisco
NAD dependent malic enzyme
NADP dependent malic enzyme
rbcL RNA S1-binding domain protein
Small subunit of Rubisco.
Raghavendra AS, Sage RF: Introduction. C4 Photosynthesis and Related CO2 Concentrating Mechanisms. Advances in Photosynthesis and Respiration, Volume 32. Edited by: Raghavendra AS, Sage RF. The Netherlands: Springer Dordrecht; 2011:17-25.
Sage RF, Zhu X-G: Exploiting the engine of C4 photosynthesis. J Exp Bot. 2011, 62: 2989-3000. 10.1093/jxb/err179.
Sage RF, Sage TL, Kocacinar F: Photorespiration and the evolution of C4 photosynthesis. Ann Rev Plant Biol. 2012, 63: 19-47. 10.1146/annurev-arplant-042811-105511.
Jones MB: C4 species as energy crops. C4 Photosynthesis and Related CO2 Concentrating Mechanisms. Advances in Photosynthesis and Respiration, Volume 32. Edited by: Raghavendra AS, Sage RF. The Netherlands: Springer Dordrecht; 2011:379-397.
Berry JO, Zielinski AM, Patel M: Gene expression in mesophyll and bundle sheath cells of C4 plants. C4 Photosynthesis and Related CO2 Concentrating Mechanisms. Advances in Photosynthesis and Respiration, Volume 32. Edited by: Raghavendra AS, Sage RF. The Netherlands: Springer Dordrecht; 2011:221-256.
Berry JO, Yerramsetty P, Zielinski AM, Mure C: Photosynthetic gene expression in higher plants. Photosyn Res. 2013, doi:10.1007/s11120-013-9880-8
Patel M, Berry JO: Rubisco gene expression in C4 plants. J Exp Bot. 2008, 59: 1625-1634.
von Caemmerer S, Furbank RT: The C4 pathway: an efficient CO2 pump. Photosyn Res. 2003, 77: 191-207. 10.1023/A:1025830019591.
Hatch MD: C4 photosynthesis: a unique blend of modified biochemistry, anatomy, and ultrastructure. Biochem Biophys Acta. 1987, 895: 81-106. 10.1016/S0304-4173(87)80009-5.
Edwards GE, Voznesenskaya EV: C4 photosynthesis: Kranz forms and single-cell C4 in terretrial plants. C4 Photosynthesis and Related CO2 Concentrating Mechanisms. Advances in Photosynthesis and Respiration, Volume 32. Edited by: Raghavendra AS, Sage RF. The Netherlands: Springer Dordrecht; 2011:29-61.
Hibberd JM, Covshoff S: The regulation of gene expression required for C4 photosynthesis. Ann Rev Plant Biol. 2010, 61: 181-207. 10.1146/annurev-arplant-042809-112238.
Langdale J: C4 Cycles: past, present, and future research on C4 photosynthesis. Plant Cell. 2011, 23: 3879-3892. 10.1105/tpc.111.092098.
Tyagi AK, Gaur T: Light regulation of nuclear photosynthetic genes in higher plants. Crit Rev Plant Sci. 2003, 22: 417-452.
Raynaud C, Loisela C, Wostrikoff K, Kuras R, Girard-Bascou J, Wollman FA, Choquet Y: Evidence for regulatory function of nucleus-encoded factors on mRNA stabilization and translation in the chloroplast. Proc Natl Acad Sci U S A. 2007, 104: 9093-9098. 10.1073/pnas.0703162104.
Johnson X, Wostrikoff K, Finazzi G, Kuras R, Schwarz C, Bujaldon S, Nickelsen J, Stern DB, Wollman F-A, Vallon O: MRL1, a conserved pentatricopeptide repeat protein, is required for stabilization of rbcL mRNA in Chlamydomonas and Arabidopsis. Plant Cell. 2010, 22: 234-248. 10.1105/tpc.109.066266.
Tillich M, Beick S, Schmitz-Linneweber C: Chloroplast RNA-binding proteins: repair and regulation of chloroplast transcripts. RNA Biol. 2010, 7: 172-178. 10.4161/rna.7.2.11090.
Barkan A: Expression of plastid genes: organelle-specific elaborations on a prokaryotic scaffold. Plant Physiol. 2011, 155: 1520-1532. 10.1104/pp.110.171231.
Slewinski TL, Anderson AA, Zhang C, Turgeon R: Scarecrow plays a role in establishing kranz anatomy in maize leaves. Plant Cell Physiol. 2013, 53: 2030-2037.
Gutteridge S, Gatenby AA: Rubisco synthesis, assembly, mechanism, and regulation. Plant Cell. 1995, 7: 809-819.
Rodermel S: Subunit control of Rubisco biosynthesis - a relic of an endosymbiotic past?. Photosyn Res. 1999, 59: 105-123. 10.1023/A:1006122619851.
Wostrikoff K, Clark A, Sato S, Clemente T, Stern D: Ectopic expression of rubisco subunits in maize mesophyll cells does not overcome barriers to cell type-specific accumulation. Plant Physiol. 2012, 160: 419-432. 10.1104/pp.112.195677.
Brown NJ, Newell CA, Stanley S, Chen JE, Perrin AJ, Kajala K, Hibberd JM: Independent and parallel recruitment of pre-existing mechanisms underlying C4 photosynthesis. Science. 2011, 331: 1436-1439. 10.1126/science.1201248.
Manuell A, Beligni MV, Yamaguchi K, Mayfield SP: Regulation of chloroplast translation: interactions of RNA elements, RNA-binding proteins and the plastid ribosome. Biochem Soc Trans. 2004, 32: 601-605. 10.1042/BST0320601.
Stern DB, Goldschmidt-Clermont M, Hanson MR: Chloroplast RNA metabolism. Annu Rev Plant Biol. 2010, 61: 125-155. 10.1146/annurev-arplant-042809-112242.
Schmitz-Linneweber C, Small I: Pentatricopeptide repeat proteins: a socket set for organelle gene expression. Trends Plant Sci. 2008, 13: 663-670. 10.1016/j.tplants.2008.10.001.
McCormac DJ, Litz H, Wang J, Gollnick PD, Berry JO: Light-associated and processing-dependent protein binding to the 5′ UTR of rbcL mRNA in the chloroplasts of a C4 plant. J Biol Chem. 2001, 276: 3476-3483. 10.1074/jbc.M009236200.
Yao W, Muqtadir K, Bruenn JA: Packaging in a yeast double-stranded RNA virus. J Virol. 1995, 69: 1917-1919.
Maai E, Miyake H, Taniguchi M: Differential positioning of chloroplasts in C4 mesophyll and bundle sheath cells. Plant Signal Behav. 2011, 6: 111-113.
Covshoff S, Furbank RT, Leegood RC, Hibberd JM: Leaf rolling allows quantification of mRNA abundance in mesophyll cells of sorghum. J Exp Bot. 2012, 64: 807-813.
Li P, Ponnala L, Gandotra N, Wang L, Si Y, Tausta SL, Kebrom TH, Provart N, Patel R, Myers CR, Reidel EJ, Turgeion R, Liu P, Sun Q, Nelson T, Brutnell TP: The developmental dynamics of the maize leaf transcriptome. Nature Genet. 2010, 42: 1060-1067. 10.1038/ng.703.
Majeran W, Friso G, Ponnala L, Connolly B, Huang M, Reidel E, Zhang C, Asakura Y, Bhuiyan NH, Sun Q, Turgeon R, Wijk KJ: Structural and metabolic transitions of C4 leaf development and differentiation defined by microscopy and quantitative proteomics in maize. Plant Cell. 2010, 22: 3509-3542. 10.1105/tpc.110.079764.
Schnable PS, Ware D, Fulton RS, Stein JC, Wei F, Pasternak S, et al: The B73 maize genome: complexity, diversity, and dynamics. Science. 2009, 326: 1112-1115. 10.1126/science.1178534.
Chang YM, Liu WY, Shih AC, Shen MN, Lu CH, Lu MY, Yang HW, Wang TY, Chen SC, Chen SM, Li WH, Ku MS: Characterizing regulatory and functional differentiation between maize mesophyll and bundle sheath cells by transcriptomic analysis. Plant Physiol. 2002, 160: 165-177.
Khalil AM, Guttman M, Huarte M, Garber M, Raj A, Morales DR, Thomas K, Presser A, Bernstein BE, van Oudenaarden A, Regev A, Lander ES, Rinn JL: Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression. Proc Natl Acad Sci U S A. 2009, 106: 11667-11672. 10.1073/pnas.0904715106.
Selth LA, Gilbert C, Svejstrup JQ: RNA immunoprecipitation to determine RNA-protein associations in vivo. Cold Spring Harb Protoc. 2009, pdb.prot5234-doi:10.1101/pdb.prot5234
Steeves TA, Sussex IM: Patterns in Plant Development. Cambridge: Cambridge University Press; 1989.
Sylvester AW, Cande WZ, Freeling M: Division and differentiation during normal and liguleless-1 maize leaf development. Development. 1990, 110: 985-1000.
Barkan A: Nuclear mutants of maize with defects in chloroplast polysome assembly have altered chloroplast RNA metabolism. Plant Cell. 1993, 5: 389-402.
Sheen J-Y, Bogorad L: Differential expression of genes for photosystem II components encoded by the plastid genome in bundle sheath and mesophyll cells of maize. Plant Physiol. 1988, 86: 1020-1026. 10.1104/pp.86.4.1020.
Li Y, Sugiura M: Three distinct ribonucleoproteins from tobacco chloroplasts: each contains a unique amino terminal acidic domain and two ribonucleoprotein consensus motifs. EMBO J. 1990, 9: 3059-3066.
Rhee SY, Beavis W, Berardini TZ, Chen G, Dixon D, Doyle A, Garcia-Hernandez M, Huala E, Lander G, Montoya M, Miller N, Mueller LA, Mundodi S, Reiser L, Tacklind J, Weems DC, Wu Y, Xu I, Yoo D, Yoon J, Zhang P: The Arabidopsis information resource (TAIR): a model organism database providing a centralized, curated gateway to Arabidopsis biology, research materials and community. Nuc Acids Res. 2003, 31: 224-228. 10.1093/nar/gkg076.
Hetherington SE, Smillie RM, Davies WJ: Photosynthetic activities of vegetative and fruiting tissues of tomato. J Exp Bot. 1999, 49: 1173-1181.
Pyke K: Mesophyll. eLS. 2012, doi:10.1002/9780470015902.a0002081.pub2
Bycroft M, Hubbard TJP, Proctor M, Freund SMV, Murzin AG: The solution structure of the S1 RNA binding domain: A member of an ancient nucleic acid–binding fold. Cell. 1997, 88: 235-242. 10.1016/S0092-8674(00)81844-9.
Yehudai-Resheff S, Portnoy V, Yogev S, Adir N, Schuster G: Domain analysis of the chloroplast polynucleotide phosphorylase reveals discrete functions in RNA degradation, polyadenylation, and sequence homology with exosome proteins. Plant Cell. 2003, 15: 2003-2019. 10.1105/tpc.013326.
Schein A, Sheffy-Leven S, Glaser F, Schuster G: The RNase E/G-type endoribonuclease of higher plants is located in the chloroplast and cleaves RNA similarly to the E. coli enzyme. RNA. 2008, 2008 (14): 1057-1068.
Chekanova JA, Dutko JA, Mian IS, Belostotsky DA: Arabidopsis thaliana exosome subunit AtRrp4p is a hydrolytic 3′–>5′ exonuclease containing S1 and KH RNA-binding domains. Nucl Acids Res. 2002, 30: 695-700. 10.1093/nar/30.3.695.
Worbs M, Bourenkov GP, Bartunik HD, Huber R, Wahl MC: An extended RNA binding surface through arrayed S1 and KH domains in transcription factor NusA. Mol Cell. 2011, 7: 1177-1189.
Stickney LM, Hankins JS, Miao X, Mackie GA: Function of the conserved S1 and KH domains in polynucleotide phosphorylase. J Bacteriol. 2005, 187: 7214-7221. 10.1128/JB.187.21.7214-7221.2005.
Eklund EA, Lee S, Skalnik DG: Cloning of a cDNA encoding a human DNA-binding protein similar to ribosomal protein S1. Gene. 1995, 155: 231-235. 10.1016/0378-1119(94)00898-3.
Majeran W, Friso G, Asakura Y, Qu X, Huang M, Ponnala L, Watkins KP, Barkan A, van Wijk KJ: Nucleoid-enriched proteomes in developing plastids and chloroplasts from maize leaves: a new conceptual framework for nucleoid functions. Plant Physiol. 2012, 158: 156-189. 10.1104/pp.111.188474.
Romanowska E, Drożak A: Comparative analysis of biochemical properties of mesophyll and bundle sheath chloroplasts from various subtypes of C4 plants grown at moderate irradiance. Acta Bioch Pol. 2006, 53: 709-719.
Simcox PD, Garland W, Deluca V, Canvin DT, Dennis DT: Respiratory pathways and fat synthesis in the developing castor-oil seed. Can J Bot. 1979, 57: 1008-1014. 10.1139/b79-125.
Ruuska SA, Girke T, Benning C, Ohlrogge JB: Contrapuntal networks of gene expression during Arabidopsis seed filling. Plant Cell. 2002, 14: 1191-1206. 10.1105/tpc.000877.
Schwender J, Goffman F, Ohlrogge JB, Shachar-Hill Y: Rubisco without the Calvin cycle improves the carbon efficiency of developing green seeds. Nature. 2004, 432: 779-782. 10.1038/nature03145.
Berry JO, Nikolau BJ, Carr JP, Klessig DF: Transcriptional and post-transcriptional regulation of ribulose 1,5-bisphosphate carboxylase gene expression in light- and dark-grown amaranth cotyledons. Mol Cell Biol. 1985, 5: 2238-2246.
Yamamoto N, Mukai Y, Matsuoka M, Kano-Murakami Y, Tanaka Y, Oshashi Y, Ozeki Y, Odani K: Light-independent expression of cab and rbcS genes in dark-grown pine seedlings. Plant Physiol. 1991, 95: 379-383. 10.1104/pp.95.2.379.
Maeda Y, Minamikawa T, Xu B-M: Metabolic activities in germinated ancient lotus seeds. J Exp Bot. 1996, 47: 577-582. 10.1093/jxb/47.4.577.
Romanowska E, Kargul J, Powikrowska M, Finazzi G, Nield J, Drozak A, Pokorska B: Structural organization of photosynthetic apparatus in agranal chloroplasts of maize. J Biol Chem. 2008, 283: 26037-26046. 10.1074/jbc.M803711200.
Kleine T, Maier UG, Leister D: DNA transfer from organelles to the nucleus: the idiosyncratic genetics of endosymbiosis. Annu Rev Plant Biol. 2009, 60: 115-138. 10.1146/annurev.arplant.043008.092119.
Zhelyazkova P, Sharma CM, Förstner KU, Liere K, Vogel J, Börner T: The primary transcriptome of barley chloroplasts: numerous noncoding RNAs and the dominating role of the plastid-encoded RNA polymerase. Plant Cell. 2012, 2012 (24): 123-136.
Mullet JE, Klein RR: Transcription and RNA stability are important determinants of higher plant chloroplast RNA levels. EMB0 J. 1987, 6: 1571-1579.
Whitney SM, Andrews TJ: The gene for the ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) small subunit relocated to the plastid genome of tobacco directs the synthesis of small subunits that assemble into Rubisco. Plant Cell. 2001, 13: 193-205.
Chalker-Scott L: Environmental significance of anthocyanins in plant stress responses. Photochem Photobiol. 1999, 70: 1-9. 10.1111/j.1751-1097.1999.tb01944.x.
Solfanelli C, Poggi A, Loreti E, Alpi A, Perata P: Sucrose-specific induction of the anthocyanin biosynthetic pathway in Arabidopsis. Plant Physiol. 2006, 140: 637-646. 10.1104/pp.105.072579.
Long JJ, Berry JO: Tissue-specific and light-mediated expression of the C4 photosynthetic NAD-dependent malic enzyme of amaranth mitochondria. Plant Physiol. 1996, 112: 473-482.
Bowman SM, Drzewiecki KD, Mojica E-R, Zielinski AM, Siegel A, Aga DA, Berry JO: Toxicity and reductions in intracellular calcium levels following?uptake of a tetracycline antibiotic in Arabidopsis. Environ Sci&Technol. 2011, 45: 8958-8964. 10.1021/es200863j.
Rodermel SR, Abbott MS, Bogorad L: Nuclear-organelle interactions: nuclear antisense gene inhibits ribulose bisphosphate carboxylase enzyme levels in transformed tobacco plants. Cell. 1988, 55: 673-681. 10.1016/0092-8674(88)90226-7.
Whitney SM, von Caemmerer S, Hudson GS, Andrews TJ: Directed mutation of the rubisco large subunit of tobacco influences photorespiration and growth. Plant Physiol. 1999, 121: 579-588. 10.1104/pp.121.2.579.
Dhingra A, Portis AR, Daniell H: Enhanced translation of a chloroplast-expressed RbcS gene restores small subunit levels and photosynthesis in nuclear RbcS antisense plants. Proc Natl Acad Sci U S A. 2004, 101: 6315-6320. 10.1073/pnas.0400981101.
Ichikawa K, Miyake C, Iwano M, Sekine M, Shinmyo A, Kato K: Ribulose 1,5-bisphosphate carboxylase/oxygenase large subunit translation is regulated in a small subunit-independent manner in the expanded leaves of tobacco. Plant Cell Physiol. 2008, 49: 214-225.
Feiz L, Williams-Carrier R, Wostrikoff K, Belcher S, Barkan A, Stern DB: Ribulose-1,5-bis-phosphate carboxylase/oxygenase accumulation factor1 is required for holoenzyme assembly in maize. Plant Cell. 2012, 24: 3435-3466. 10.1105/tpc.112.102012.
Foyer CH, Neukermans J, Queval G, Noctor G, Harbinson J: Photosynthetic control of electron transport and the regulation of gene expression. J Exp Bot. 2012, 63: 1637-1661. 10.1093/jxb/ers013.
Barnes D, Mayfield SP: Redox control of posttranscriptional processes in the chloroplast. Antiox Redox Sig. 2003, 5: 89-94. 10.1089/152308603321223577.
Raghavendra AS: Padmasre: beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation. Trends Plant Sci. 2003, 8: 546-553. 10.1016/j.tplants.2003.09.015.
Puthiyaveetil S, Ibrahim IM, Allen JF: Oxidation–reduction signalling components in regulatory pathways of state transitions and photosystem stoichiometry adjustment in chloroplasts. Plant Cell Environ. 2012, 35: 347-359. 10.1111/j.1365-3040.2011.02349.x.
Rossel JB, Wilson IW, Pogson BJ: Global changes in gene expression in response to high light in Arabidopsis. Plant Physiol. 2002, 130: 1109-1120. 10.1104/pp.005595.
Liu M-J, Wu S-H, Chen H-M, Wu S-H: Widespread translational control contributes to the regulation of Arabidopsis photomorphogenesis. Mol Sys Biol. 2012, 8: 566-
Park SH, Chung PJ, Juntawong P, Bailey-Serres J, Kim YS, Jung H, Bang SW, Kim YK, Do Choi Y, Kim JK: Posttranscriptional control of photosynthetic mRNA decay under stress conditions requires 3′ and 5′ untranslated regions and correlates with differential polysome association in rice. Plant Physiol. 2012, 159: 1111-1124. 10.1104/pp.112.194928.
Paul MJ, Foyer CH: Sink regulation of photosynthesis. J Exp Bot. 2001, 52: 1383-1400. 10.1093/jexbot/52.360.1383.
Maier A, Zell MB, Maurino VG: Malate decarboxylases: evolution and roles of NAD(P)-ME isoforms in species performing C4 and C3 photosynthesis. J Exp Bot. 2010, 62: 3061-3069.
Weissmann S, Brutnell TP: Engineering C4 photosynthetic regulatory networks. Curr Opin Biotechnol. 2012, 23: 298-304. 10.1016/j.copbio.2011.12.018.
Lee KP, Kim C, Landgraf F, Apel K: EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana. Proc Natl Acad Sci U S A. 2007, 104: 10270-10275. 10.1073/pnas.0702061104.
Slesak I, Libik M, Karpinska B, Karpinski S, Miszalski Z: The role of hydrogen peroxide in regulation of plant metabolism and cellular signaling in response to environmental stresses. Acta Biochim Pol. 2007, 54: 39-50.
Piippo M, Allahverdiyeva Y, Paakkarinen V, Suoranta UM, Battchikova N, Aro EM: Chloroplast-mediated regulation of nuclear genes in Arabidopsis thaliana in the absence of light stress. Physiol Genom. 2006, 25: 142-152. 10.1152/physiolgenomics.00256.2005.
Acevedo-Hernandez GJ, Leon P, Herrera-Estrella LR: Sugar and ABA responsiveness of a minimal RBCS light-responsive unit is mediated by direct binding of ABI4. Plant J. 2005, 43: 506-519. 10.1111/j.1365-313X.2005.02468.x.
Langdale JA, Kidner CA: Bundle sheath defective, a mutation that disrupts cellular differentiation in maize leaves. Development. 1994, 120: 673-681.
May BP, Martienssen RA: Transposon mutagenesis in the study of plant development. Crit Rev Plant Sci. 2003, 22: 1-35. 10.1080/713610849.
Lisch D: Mutator transposons. Trends Plant Sci. 2002, 11: 498-504.
Barkan A, Martienssen RA: Inactivation of maize transposon Mu suppresses a mutant phenotype by activating an outward-reading promoter near the end of Mu1. Proc Natl Acad Sci U S A. 1991, 88: 3502-3506. 10.1073/pnas.88.8.3502.
Ortiz DF, Strommer JN: The Mu1 maize transposable element induces tissue-specific aberrant splicing and polyadenylation in two Adh1 mutants. Mol Cell Biol. 1990, 10: 2090-2095.
Hudson GS, Mahon JD, Anderson PA, Gibbs MJ, Badger MR, Andrews T, Whitfeld PR: Comparisons of rbcL genes for the large subunit of ribulose-bisphosphate carboxylase from closely related C3 and C4 plant species. J Biol Chem. 1990, 265: 808-814.
Patel M, Corey AC, Yin L-Y, Ali S, Taylor WC, Berry JO: Untranslated regions from C4 amaranth AhRbcS1 mRNAs confer translational enhancement and preferential bundle sheath cell expression in transgenic C4Flaveria bidentis. Plant Physiol. 2004, 136: 3550-3561. 10.1104/pp.104.051508.
Wang J-L, Klessig DF, Berry JO: Regulation of C4 gene expression in developing amaranth leaves. Plant Cell. 1992, 4: 173-184.
McCormac DJ, Boinski JJ, Ramsperger VC, Berry JO: C4 Gene expression in photosynthetic and non-photosynthetic leaf regions of Amaranthus tricolor. Plant Physiol. 1997, 114: 801-815.
Wesley SV, Helliwell CA, Smith NA, Wang NB, Rouse DT, Liu Q, Gooding PS, Singh SP, Abbott D, Stoutjesdijk PA, Robinson SP, Gleave AP, Green AG, Waterhouse PM: Construct design for efficient, effective and high-throughput gene silencing in plants. Plant J. 2001, 27: 581-590. 10.1046/j.1365-313X.2001.01105.x.
Bent A: Arabidopsis thaliana floral dip transformation method. Methods Mol Biol. 2006, 343: 87-103.
Barkan A: Approaches to investigating nuclear genes that function in chloroplast biogenesis in land plants. Meth Enzymol. 1998, 297: 38-57.
Barkan A: Genome-wide analysis of RNA-protein interactions in plants. Meth Mol Biol. 2009, 553: 13-37. 10.1007/978-1-60327-563-7_2.
We are grateful to Masahiro Sugiura, Julian Hibbard, and Richard Leegood for their generous gifts of antisera. We thank Jim Stamos for preparation of the Figures, Alan Siegel for Confocal Microscopy support, Dennis Pietras for plant care, and Margaret Hollingsworth for critical reading of the manuscript. We thank Victor Albert for the use of his facilities and instrumentation for qRT-PCR. This work was supported by USDA/NRI Grant 2008–01070 and NSF grant MCB 0544234 to J.O.B. The Zeiss LSM 710 “In Tune” Confocal Microscope used for imaging of the immunolocalizations was purchased through NSF Major Research Instrumentation grant DBI 0923133. AMZ was supported by a graduate fellowship through the Interdisciplinary Science and Engineering Partnership (ISEP), an NSF Math Science Partnership program, #DUE 1102998. We thank Tiffany Kroeger and Susan Belcher at the maize Photosynthetic Mutant Library (PML, University of Oregon, supported by NSF grant #I0S-0922560 to Alice Barkan) for identifying and providing the maize mutants, and Alice Barkan for useful discussion and advice in the use and analysis of the mutants.
The authors declare that they have no competing interests.
SMB, MP, and JOB designed and oversaw the research. SMB, MP, PY, CMM, AMZ, and JOB performed the research. CM and JAB performed bioinformatics analysis, including database searches and sequence alignments. SMB, MP, PY, CMM, AMZ, and JOB wrote the article. All authors read and approved the final manuscript.
Shaun M Bowman, Minesh Patel, Pradeep Yerramsetty contributed equally to this work.
Electronic supplementary material
Additional file 3: Figure S3: Genomic sequence of maize RBCL RNA S1-BINDING DOMAIN PROTIEN (RLSB) gene (GRMZM2G087628, from Maize Genomic BAC AC211368.4), with Mu inserts. Green = Exon coding regions, Blue = introns, Black = non-coding or non-transcribed sequences, *1 = rblmsb1 insert; *2 = rblmsb2 insert. ATG and TAA are in bold and underlined. (PDF 37 KB)
Additional file 6: Figure S6: Accumulation of plastid-encoded mRNA and rRNA in lower leaf regions from RLSB/RLSB and rlsb-1/rlsb-2 maize seedlings. A. Accumulation of several plastid-encoded mRNAs. B. Accumulation of plastid-encoded rRNAs. C. Formaldehyde-agarose gel, transferred to nitrocellulose and stained with methylene blue, showing cytoplasmic and chloroplast rRNAs in two RLSB/RLSB plants and three rlsb-1/rlsb-2 mutant plants. 28S and 18S are cytoplasmic rRNAs. 16S rRNA and the 23S* cleavage product of 23S rRNA are chloroplastic. For qRT-PCR shown in A and B, quantification of transcript levels was standardized to actin mRNA. Data is averaged for two RLSB/RLSB plants and four rlsb-1/rlsb-2 siblings, with three repeats run for each of the plant samples. Note differences in scale for panels A and B, due to the much greater abundance of rRNA relative to the mRNAs. Statistical significance was calculated using Student’s t-test. For each bar, P values were less than 0.05. (PDF 227 KB)
Additional file 7: Figure S7: Low magnification immunolocalization image of RLSB and Rubisco LSU proteins in leaf sections of the C3 plant Arabidopsis. A. Arabidopsis leaf section reacted with RLSB primary antiserum. B. Arabidopsis leaf sections reacted with LSU primary antiserum. C. Arabidopsis leaf section showing autofluorescence of plastids (imaged enhanced) from a section reacted with secondary antibody alone. D. DIC image of the images shown in A and C, with chloroplasts indicated. cp, chloroplasts. Arabidopsis leaf sections were incubated with the indicated primary antiserum, and then with R-phycoerythrin (A, B) conjugated secondary antibody. Images were captured using a 20X objective of a Leica DMIRE2 inverted fluorescent microscope, bar = 100 μM. (PDF 884 KB)
Additional file 8: Figure S8: Rubisco protein and mRNA accumulation in rlsb T-DNA insertion heterozygotes, non-mutant siblings, and wild type Col0 Arabidopsis. A. Western analysis. Total protein from heterozygous SALK_015722 containing a T-DNA insert in one copy of the RLSB locus, and wild type non-insert containing plants reacted with LSU antisera (top panels). Equal amounts of protein were loaded in each lane. As a control, the blot was re-probed with actin antisera (bottom panels). B. Segregating wild type siblings lacking T-DNA inserts showed no LSU reduction. C. qRT-PCR analysis of rbcL mRNA in wild type and SALK_015722 heterozygotes. For each plant, random primers produced cDNA from mRNA; these were then incubated with primers for Arabidopsis rbcL mRNAs, or for plastid-encoded rps3 and rpl20 (standardization controls). For each bar, P values were less than 0.05. D. Genomic PCR analysis of T-DNA insert in At1g71720 locus. Ethidium-bromide stained agarose gel showing representative PCR amplifications using total DNA isolated from the indicated plants. The three primers added to each PCR reaction were: LP (At1g71720 sequence upstream of insert site) = TCGATTGCTGATTTTGATTCC; RP (At1g71720 sequence downstream of insert site) = TTCCTTCCCCTTTTTCATGTC; LBB1 (left border of T-DNA) = GCGTGGACCGCTTGCTGCAACT (Reverse AGTTGCAGCAAGCGGTCCACGC). Sequencing confirmed the identity of the amplified fragments. A 261 nucleotide band corresponding to wild type At1g71720 was amplified from LP and RP primers if there was no insert; A 128 nt band was amplified from LP and LBB1 if the locus contained an insert. Lane 1 = wt Col0 (normal LSU levels), showing a band of 261 nt. Lane 2 = heterozygote AT SALK 017226 (reduced LSU), showing two amplified bands of 261 and 128 nt. Lane 3 = AT SALK 017226 segregate (sibling plant with normal LSU levels and no T-DNA insert), showing a single amplified band at 261 nt. (PDF 287 KB)
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Bowman, S.M., Patel, M., Yerramsetty, P. et al. A novel RNA binding protein affects rbcL gene expression and is specific to bundle sheath chloroplasts in C4plants. BMC Plant Biol 13, 138 (2013). https://doi.org/10.1186/1471-2229-13-138
- C4 photosynthesis
- S1-domain RNA binding protein
- rbcL gene expression
- Cell-type specificity
- Post transcriptional control
- C4 maize