Identification and characterization of nuclear genes involved in photosynthesis in Populus
© Wang et al.; licensee BioMed Central Ltd. 2014
Received: 15 September 2013
Accepted: 17 March 2014
Published: 27 March 2014
The gap between the real and potential photosynthetic rate under field conditions suggests that photosynthesis could potentially be improved. Nuclear genes provide possible targets for improving photosynthetic efficiency. Hence, genome-wide identification and characterization of the nuclear genes affecting photosynthetic traits in woody plants would provide key insights on genetic regulation of photosynthesis and identify candidate processes for improvement of photosynthesis.
Using microarray and bulked segregant analysis strategies, we identified differentially expressed nuclear genes for photosynthesis traits in a segregating population of poplar. We identified 515 differentially expressed genes in this population (FC ≥ 2 or FC ≤ 0.5, P < 0.05), 163 up-regulated and 352 down-regulated. Real-time PCR expression analysis confirmed the microarray data. Singular Enrichment Analysis identified 48 significantly enriched GO terms for molecular functions (28), biological processes (18) and cell components (2). Furthermore, we selected six candidate genes for functional examination by a single-marker association approach, which demonstrated that 20 SNPs in five candidate genes significantly associated with photosynthetic traits, and the phenotypic variance explained by each SNP ranged from 2.3% to 12.6%. This revealed that regulation of photosynthesis by the nuclear genome mainly involves transport, metabolism and response to stimulus functions.
This study provides new genome-scale strategies for the discovery of potential candidate genes affecting photosynthesis in Populus, and for identification of the functions of genes involved in regulation of photosynthesis. This work also suggests that improving photosynthetic efficiency under field conditions will require the consideration of multiple factors, such as stress responses.
Addressing global concerns regarding crop yield and fossil fuel energy will require novel strategies. Photosynthesis harnesses solar energy, produces carbohydrates and biomaterials and sustains the carbon/oxygen cycle; supercharging photosynthesis may help to address these concerns and meet increasing demands for food, fuel, and biomaterials [1, 2]. Improving photosynthesis in annual, herbaceous crops would provide substantial benefits, as more than 90% of crop biomass derives from photosynthetic products . The woody tissues of trees make up roughly 20% of the total terrestrial carbon storage [4, 5], and also derive from photosynthetic products. Therefore, improving photosynthesis in perennial, woody crops would improve carbon fixation, biomaterials production, and biofuels efficiency.
Despite its importance, photosynthesis has inefficiencies: plants typically convert only 2% to 4% of the available solar energy into plant growth . The gap between the real and potential photosynthetic rate under field conditions suggests that photosynthesis could be improved to increase crop yields and improve the economics of biofuel production. However, the complex process of photosynthesis includes many potential target reactions, such as light harvesting, carbon fixation, photophosphorylation and electron transport . Potential ways to improve photosynthesis include directly improving the mechanism of photosynthesis itself , or exploring and analyzing the complexity of photosynthetic regulation in the field to improve photosynthesis from a whole-plant perspective. Studies exploring improvements to the mechanism of photosynthesis have been widely reported [2, 7]. Current proposals to improve photosynthesis mainly include improving the performance of Rubisco , decreasing photorespiration  and adding new biosynthetic pathways to increase the flow of carbon into useful products . However, efforts to improve chloroplast-related processes may be constrained by known and unknown factors. For example, increasing photosynthetic rates by engineering photosynthetic pathways may overburden the capacity of the transport systems inside and outside of the chloroplast . Exploring and analyzing the complexity of photosynthetic regulation in field conditions may identify these constraints and allow researchers to bypass potential difficulties.
The role of the nucleus should command particular attention among the mechanisms regulating photosynthesis. The chloroplast, as the site of photosynthesis, requires adaptive changes in the expression levels of nuclear genes to respond to endogenous and environmental stimuli; a complex signaling network regulates these changes in gene expression [11–13]. Chloroplast and chloroplast-related processes have been studied in detail . The higher plant nuclear genome encodes about 2,090 predicted chloroplast proteins (http://rarge.psc.riken.jp/chloroplast/), and chloroplast metabolism is tightly integrated with the rest of the cell (http://www.grenoble.prabi.fr/at_chloro/) [15, 16]. Hence, the nucleus plays a crucial role in maintaining normal function of the chloroplast [17, 18].
Nuclear genes provide potential targets for improving photosynthetic efficiency. For example, Rubisco, the enzyme that catalyzes the reaction of CO2 into ribulose 1,5-bisphosphate (RuBP), is a prime target for genetic engineering to improve photosynthetic efficiency , but the locations of rbcL in the chloroplast genome and RbcS in the nuclear genome have hindered this approach . Various other biological processes regulated by the nucleus  also may be useful targets for improving photosynthesis, such as plant morphology , photoprotection , and the regulation of photosynthesis by the sophisticated balance of energy  and redox . However, the nuclear genes involved in the regulation of photosynthesis remain poorly understood, especially in trees, despite the importance of nuclear genes in all photosynthesis-related processes. Trees are extremely long-lived and generate woody biomass derived from plant cell wall lignocellulose. So, in trees, the mechanisms of nuclear regulation of photosynthesis may be even more complicated than in herbaceous annuals.
Studies of the regulation of photosynthesis have mainly focused on the influence of environmental factors or the interaction with other biological processes. Most stresses, including biotic , chilling , drought  and salt  stress, repress photosynthesis. Ecosystem respiration is tightly coupled with canopy photosynthesis . Also, transport mechanisms and efficiency influence photosynthetic productivity by relieving product inhibition and contribute to plant vigor by controlling source/sink relationships and biomass partitioning . However, little is known about the role of nuclear genes in photosynthesis. Populus, as a model for long-lived woody perennials , can be used to study the molecular basis of regulation of photosynthesis at the genome scale in woody plants. Based on the high-quality, annotated genome sequence of Populus trichocarpa, emerging research has investigated biological functions in woody plants including wood formation, seasonality, flowering control, dormancy release, senescence, biotic interactions and abiotic stress responses .
In the present study, we used a segregating population of poplars with different net photosynthetic rates (Pn), to identify and characterize nuclear genes involved in photosynthesis in trees, by combining microarray techniques and bulked segregant analysis (BSA). To our knowledge, this is the first systematic, genome-wide investigation of differentially expressed genes in pools of progeny with different photosynthetic rates in Populus. We identified 515 differentially expressed genes in this population according to the fold change (FC) of gene expression (FC ≥ 2 or FC ≤ 0.5, P < 0.05). Also, we outlined a putative gene network in the Populus nuclear genome for regulation of photosynthesis. Furthermore, the differentially expressed genes identified here may be suitable targets for biotechnological manipulation to improve photosynthesis.
Phenotypic variation and correlation
For this study, we used a linkage mapping population of 1200 F1 progeny, from the cross of two elite poplar parents, the female hybrid clone “YX01” (P. alba × P. glandulossa) and the male clone “LM50” (P. tomentosa). We first characterized the variation in photosynthetic characteristics, including Pn, stomatal conductance (Cond), intercellular CO2 concentration (Ci) and transpiration rate (Trmmol), in this population. The photosynthetic characteristics Pn, Cond, Ci, and Trmmol of the 1200 F1 individuals had a continuous distribution indicating that all measured traits were quantitatively inherited and each trait showed significant differences in the population (Additional file 1: Figure S1). Means of the four photosynthetic characteristics were: 13.360 ± 0.116 (mean ± SE) μmol · m−2 · s−1 (Pn), 0.225 ± 0.003 mol · m−2 · s−1 (Cond), 243.203 ± 2.026 μmol · mol−1(Ci), and 4.571 ± 0.047 g · m−2 · h−1 (Trmmol) and their coefficients of variation (CV) ranged from 27.755% to 49.333%. The CV of Pn and Ci were similar, at 28.915% and 27.755%, respectively (Additional file 2: Table S1). We also measured three growth traits and four wood property traits. CVs of growth traits including tree height (H), diameter at chest height (D) and stem volume (V) were 25.403%, 29.464% and 78.630% respectively. For D, we define “chest height” as 1.3 meters above the ground. Wood traits showed lower CVs; for example, the CV of holocellulose content was the smallest, at just 1.941%. Descriptive statistics of the trait distributions are presented in Additional file 2: Table S1. The broad sense heritability (h2) was estimated for each trait (Additional file 3: Table S2) ranged from 65.76% to 99.97%. Pn had the highest h2 value, followed by Cond, V, D, Trmmol, H, Ci, Lignin content, microfiber angle and α-cellulose content. The h2 of holocellulose content was lowest. Higher h2 values were observed in photosynthetic characteristics and growth traits (D, H, V).
Phenotypic (above the diagonal) and genetic (below the diagonal) correlations for photosynthetic characteristics and wood traits in the linkage mapping population (n = 300)
Identification of differentially expressed genes
To find nuclear genes involved in photosynthesis, we compared the gene expression profiles of pools constructed by bulked segregant analysis (BSA) . Specifically, we identified plants with very high and very low photosynthetic rate (Pn). Plants with high or low Pn were pooled and compared. Microarray-based comparison of the FC of gene expression between the pools with high and low photosynthetic efficiency showed that only 0.84% of all probes (515 out of 61,313) showed a significant difference (FC ≥ 2 or FC ≤ 0.5, P < 0.05). Of these, 162 probes were up-regulated (see Additional file 4) and 353 were down-regulated (see Additional file 5) in plants with high Pn, compared to the plants with low Pn. The fact that most of the significantly differentially expressed genes were repressed in plants with high Pn (68.54%) may be explained because plants under field conditions rarely realize their maximum photosynthetic potential . Of the differentially expressed genes, 74 were annotated as having no known function (unknown proteins, hypothetical proteins, etc.) and of these, 30 (40.54%) were up-regulated (see Additional file 4), suggesting that they were bona fide candidates for novel, up-regulated photosynthesis genes.
Verification of the differentially expressed genes identified by microarray
GO analysis and co-expression patterns
Gene ontology enrichment analysis of the differentially expressed genes
Number in input list
Number in BG/Ref
chitin metabolic process
chitin catabolic process
aminoglycan catabolic process
aminoglycan metabolic process
carbohydrate metabolic process
polysaccharide metabolic process
cell wall macromolecule metabolic process
cell wall macromolecule catabolic process
cell wall organization or biogenesis
polysaccharide catabolic process
primary metabolic process
negative regulation of molecular function
negative regulation of catalytic activity
macromolecule metabolic process
carbohydrate catabolic process
hydrolase activity, hydrolyzing O-glycosyl compounds
enzyme inhibitor activity
hydrolase activity, acting on glycosyl bonds
enzyme regulator activity
sequence-specific DNA binding
endopeptidase inhibitor activity
peptidase inhibitor activity
protein tyrosine kinase activity
iron ion binding
identical protein binding
serine-type peptidase activity
serine hydrolase activity
metal ion binding
transcription factor activity
external encapsulating structure
Categories of differentially expressed genes involved in photosynthesis
The differentially expressed genes involved in photosynthesis were enriched in some groups including genes coordinating with organelles, and genes related to: the plant cell wall, response to stimulus, transport and redox. We also looked for organellar proteins and found 72 differentially expressed genes that encode proteins with known Arabidopsis homologs that localize in the chloroplast and/or mitochondrion (see Additional file 9). Gene expression ratios for the putative organellar proteins varied from 0.080- to 0.498- and 2.023- to 8.047-fold. A representation of the differentially expressed genes is shown in Additional file 10: Figure S2A. Of these, 80.95% of mitochondrion-located genes were down-regulated (Additional file 10: Figure S2B). This reveals that regulatory functions may be coordinated between nuclei and organelles in photosynthesis. We also identified 82 differentially expressed genes involved in cell wall functions (see Additional file 11). The SEA analysis in all different expression genes showed that cell wall macromolecule catabolic process (GO:0016998), cell wall macromolecule metabolic process (GO:0044036) and cell wall organization or biogenesis (GO:0071554) were significantly enriched GO terms (Table 2). However, the up- and down-regulated genes showed different related biological processes; most of the up-regulated genes related to plant cell wall growth and most of the down-regulated genes related to response for stimulus (Additional file 12: Figure S3, Additional file 11).
Transporters perform many important physiological functions, including the transport and distribution of photosynthetic assimilates. Hence, it was no surprise that genes related to transport were identified. We detected 45 differentially expressed genes (8.74% in all identified genes) related to transport (see Additional file 14). Gene families of these differentially expressed genes included ABC (ATP-Binding cassette), MFS (major facilitator superfamily protein), MIP (major intrinsic protein), OPT (oligopeptide transport), SLAH (S-type anion channel), PIN and other families. Most of the down-regulated genes encoded proteins predicted to locate in the membrane and conduct energy-related transport. This suggested that genes related to transport also affect photosynthetic rate. Photosynthesis has a high risk for producing photo-oxidative damage and generates redox intermediates with strong redox potentials (see Additional file 15). GO term enrichment analysis revealed that the biological process ‘oxidation reduction’ (GO:0055114, P = 0.0015) was also significantly enriched (Table 2). Four genes encoding glutathione transferase, one encoding glutathione and one encoding glutathione-dependent formaldehyde dehydrogenase were detected and all were slightly repressed in plants with high Pn, from 0.24- to 0.45-fold (see Additional file 15). Also, three NADH dehydrogenases, two NADH/Ubiquinone/plastoquinones (complex I) and two NADPH oxidases were repressed (see Additional file 15). This suggested that the regulation of redox plays a crucial role in photosynthesis.
Polymorphic SNP loci associated with traits affecting photosynthesis
Significant SNP marker-trait associations tested in the population (n = 300) after a correction for multiple testing [false discovery rate FDR ≤ 0.10]
Phenotypic variation (%)
Leu to Pro
Ala to Pro
Ala to Val
Glu to Gln
Met* to Val
Ala to Pro
Ala to Val
Glu to Gln
Met* to Val
Glu to Gln
Ala to Val
Met* to Val
Regulatory network of nuclear genes involved in photosynthesis
Our study identified 515 nuclear genes involved in photosynthesis in Populus under field conditions. Based on our analysis of these differentially expressed genes, we constructed a gene network (Figure 5), which revealed the role of nuclear genes involved in photosynthesis under field conditions in Populus. The major processes identified by these genes include response to stimulus, metabolism, and transport. This study provides new genome-scale strategies for the discovery of potential candidate genes affecting photosynthesis in Populus, and also for identification of gene functions involved in the regulation of photosynthesis.
Genes coordinating with organelles
Enzymatic and photosynthetic complexes within chloroplasts contain subunits encoded by the nuclear and plastid genomes , and chloroplasts and mitochondria interact with the nucleus. Hence, we compared our study with previous studies to find genes involved in coordinating nuclear functions with organelles (chloroplast and/or mitochondrion) at the genome scale under field conditions. We detected 72 differentially expressed genes encoding putative organellar proteins (Additional file 10: Figure S2A). The largest groups of differentially expressed genes included genes involved in metabolism (18.31%, e.g. NADP+-isocitrate dehydrogenase, sulfotransferase 2A), photosynthesis (23.94%, e.g. chlorophyllase, PsbP-like protein 1) and genes with unknown function (19.72%) (Additional file 9). Of these, 80.95% of mitochondrion-located genes were down-regulated (Additional file 10: Figure S2B) including acyl activating enzyme (FC = 0.106), enoyl-CoA hydratase/isomerase (FC = 0.432), and cytochrome P450 (FC = 0.120). Most of these genes play particularly important roles in different metabolic processes, including energy metabolism or downstream molecular functions affecting metabolic processes. For example, enoyl-CoA hydratase/isomerase indicates an effect on the β-oxidation pathway, which might change carbon flux (in the form of acetyl-CoA) entering the tricarboxylic acid cycle . The large cytochrome P450 of plant metabolic enzymes catalyze a huge variety of oxidation reactions in microbes and higher organisms . Mitochondrial oxidative metabolism modulates the coordination between different components of photosynthetic carbon assimilation in chloroplasts, such as generation and use of assimilatory power (ATP and NADPH), induction of photosynthesis, maintenance of metabolites and the light activation of Calvin cycle enzymes [40, 41]. The above considerations indicate that the mitochondrion plays an important role in photosynthesis.
As expected, we detected nuclear genes involved construction or development of chloroplasts (e.g., senescence-inducible chloroplast stay-green protein, PsbP-like protein) (see Additional file 9). For example, the gene encoding ATP-dependent Clp protease regulatory subunit, an essential housekeeping enzyme in chloroplasts , was down-regulated by 0.45-fold. PsbP-like protein is an extrinsic subunit of eukaryotic photosystem II (PSII) and participates in the normal function of photosynthetic water oxidation; the up-regulation of this gene (2.14-fold) revealed that nuclear genes control photosynthesis by affecting the structure or development of chloroplasts.
We found that co-ordination between the nucleus and chloroplast was a crucial but small part of the nuclear regulation of photosynthesis. We did not identify significant GO terms involving chloroplast-related processes. After comparing our results to a previous study, we identified just 20 genes (e.g., chloroplast precursor, potassium channel KAT3, and phosphate-responsive 1 family protein) in the analysis of 101 nuclear transcriptomes, which revealed 23 distinct regulons and their relationship in coordination of nuclear and plastid gene expression  (Additional file 19: Table S8). However, genes related to other complex biological processes were identified in our study. Hence, we consider the regulation of photosynthesis in trees should be viewed on a whole-plant scale.
The role of the cell wall in photosynthesis
We identified 82 differentially expressed genes involved in cell wall functions (Additional file 11). Although a similar number of genes were up- (39) and down-regulated (43) (Additional file 12: Figure S3), the constitution of related biological processes clearly differed. Most of the up-regulated genes were related to plant cell wall growth, such as expansins (FC = 2.009 to 5.536) and xyloglucan endotransglycosylase (FC = 2.192 to 11.412). Conversely, most of the down-regulated genes were related to response for stimulus, such as chitinase (FC = 0.148 to 0.422) and pathogenesis-related protein (FC = 0.046). This revealed that photosynthesis may be positively correlated with growth and negatively correlated with stress.
As expected, we detected genes related to carbohydrate active enzymes (CAZYmes), which function in the formation and modification of the carbohydrate matrix of wood cell walls, including genes encoding cellulose synthase-like (CSLs), pectin methyl esterases (PMEs), xyloglucan endo-transglucosylases and hydrolases (XETs and XEHs), and expansins . These proteins play crucial roles in assimilating the products of photosynthesis into sugars and starch, in synthesizing cell wall biopolymers and in creating various glycosylated compounds . Most of the carbohydrate-related genes (75%) were slightly up-regulated, by 2.01- to 11.41-fold, indicating that high photosynthetic rate was related to carbohydrate activity. Of these, CSLs (FC = 2.69- to 2.70-fold), which are good candidates for the synthases forming the β-D-glycan backbone of hemicelluloses such as xyloglucan, xylan, mannan and other β-D-glycans in the cell wall, were up-regulated . PMEs, which were among the up and down-regulated genes, have major roles in pectin remodeling . These genes influence cell wall remodeling, which may largely contribute to internal carbon recycling and thus ultimately affect photosynthesis .
XET specifically cuts the backbone of xyloglucan and re-forms a glycosidic bond with the free end of another xyloglucan chain . We found that the gene encoding XET was up-regulated by up to 11.41-fold in the poplars with higher photosynthetic efficiency. As the most abundant hemicellulose in the primary cell wall in many dicotyledonous plants, xyloglucan has a backbone of β1 → 4-linked glucose residues. This may be affected by sugar signaling pathways, as sucrose is the major photosynthetic product and affects growth and metabolism . This also supports the present result that four SNP markers from a xyloglucan endotransglycosylase precursor (XET16A) showed a significant association with four photosynthetic characteristics (Table 3). Of these, a significant SNP (XET-SNP3) detected in the 5′ UTR may affect many post-transcriptional regulatory pathways. The T-C mutation in XET-SNP5 causes a leucine to proline amino acid substitution and the G-C mutation at XET-SNP6 causes an alanine to proline substitution. These findings suggest that XET may function downstream of photosynthesis and play an important role in the balance of glucose. In Populus, at least 16 XTH genes, likely encoding XETs, were expressed in developing xylem, indicating that the amount of nascent xyloglucan relative to XET was an important determinant of whether XET strengthens or loosens the cell wall . This supports the idea that this gene is involved in photosynthesis in Populus.
We found that of the genes down-regulated in plants with high photosynthetic efficiency were related to stress responses, such as PI (proteinase inhibitor), chitinase  and pathogenesis-related protein , and the fold change of these genes was as low as 0.03 (PR-6 proteinase inhibitor). Of these, PI-SNP1, a noncoding marker within a gene from the PR-6 proteinase inhibitor family constituting a sub-class of serine PIs with characteristics of potato/tomato type I PIs , was the only single-marker association with a growth trait (H) in single marker analysis (Table 3). Plants stringently govern PI activity to achieve cellular homeostasis. We suppose that PI activity relates to tree height through its effect on the water-stress response. Current hypotheses for tree height limitation focus on increasing water transport constraints in taller trees and the resulting reductions in leaf photosynthesis . Also, PIs were up-regulated under water stress both in soybean  and maize .
Photosynthesis and hormone
Plant hormones, a group of chemically diverse small molecules, direct processes ranging from growth and development to biotic and abiotic stress responses. In this study, the stimulus response category related to hormone responses included SAUR (small auxin up-regulated RNA), AUX (auxin response gene family), GASA (gibberellin-regulated protein), GID (gibberellin receptor) and some genes responding to other hormones (Additional file 13). The genes showed clear differences between up- and down-regulated gene sets. For instance, all the GIDs were down-regulated and the vast majority of SAUR, AUX and GASA genes, which function in different processes throughout plant growth and development , were up-regulated. For example, SAURs function as primary auxin response genes hypothesized to be involved in auxin signaling pathways. They were up-regulated by 2.32- to 3.98-fold. Genes encoding auxin efflux carrier family proteins were also up-regulated, suggesting that photosynthetic activity might increase auxin content to affect development . The effect of GA on photosynthesis has been controversial [60–63]. In our study, a gene encoding GASA was up-regulated by 4.03-fold. The SNP marker in GASA showed a significant association with two photosynthetic traits (Table 3). Phenotypic variance for Cond and Pn explained by the GASA-SNP3 marker was up to 12.6% and 8.0%, respectively. Our result supports the idea that photosynthesis was at least indirectly GA-responsive, an idea further supported by a study in which GA3 treatment increased photosynthetic activity .
Photosynthesis and stress
Environmental factors limit photosynthesis, so plants rarely realize their maximum photosynthetic potential under field conditions . Hence, it was not surprising that we found genes related to stress in this study. Stress-related genes likely play roles in protecting photosynthetic functions, metabolizing the factors that inhibit photosynthesis [25, 29] and maintaining cell homeostasis. For example, we found that peroxiredoxin was down-regulated by 0.02-fold in the poplars with high photosynthetic efficiency (Additional file 15). It encodes peroxiredoxin Q, which decomposes peroxides and plays a role in the protection of the photosynthetic apparatus . Also glutathione-transferase (GST) (down-regulated by 0.24- to 0.45-fold) is induced by diverse environmental stimuli, with increased GST levels used to maintain cell redox homeostasis and protect organisms from oxidative stress, which can seriously affect leaf photosynthetic machinery . Also, we found that nuclear genes affect endogenous and environmental stimuli and regulate key proteins responding to stress. We detected 14 WRKY transcription factors, important functional components for plant stress responses, as being down-regulated. WRKYs relate to tolerance to wounding, heat, cold, NaCl, sugar, drought, oxidative stress and others  (see Additional file 20).
SEA analysis showed an enrichment of terms involving chitinase, such as chitin catabolic process (GO:0006032), chitin metabolic process (GO:0006030), chitinase activity (GO:0004568) and chitin binding (GO:0008061) (Table 2). Chitinase protects plants against fungal pathogens by degrading chitin, a major component of the cell walls of many fungi (see Additional file 11). Fragments from chitin and chitosan have elicitor activities leading to a variety of defense responses in host plants in response to microbial infection , including induction of pathogen-related proteins and PI, which were also identified in this study.
Most genes involved in stress response were down-regulated, such as PI, chitinase, peroxidase, heat shock protein  and pathogenesis-related protein. For example, all six genes encoding peroxidase, a plant-specific oxidoreductase affecting responses to environmental stimuli , were repressed, down to 0.01-fold. Also, peroxiredoxins play important roles in plant development, environmental adaptation, and disease resistance , and this gene was repressed too. This result could be considered from two aspects. First, low photosynthetic rate led to less production of sugar and energy, resulting in a decline in plant adaptability . Second, plants with good environmental adaptability could grow and thus had a high photosynthetic rate. All the above results suggest that nuclear regulation of the response for stress is an important part of photosynthesis. This suggests that improving plant stress tolerance may enhance photosynthetic efficiency in field conditions.
Photosynthesis and metabolism
The relationship between metabolism and photosynthesis is complex, involving photosynthate production (e.g., carbohydrates, proteins, amino acids etc.), energy and nutrition. Cell wall carbohydrate metabolic processes were highlighted in this study. This suggests that nuclear genes may affect photosynthesis by regulating polysaccharides in the cell wall for a possible source of sugar. For example, the identified cell wall-bound β-glucosidase was repressed (FC = 0.07-fold) in high photosynthetic rate pools (see Additional file 11). It breaks down polysaccharides to soluble sugars when photosynthesis declines. Also, reduced photosynthesis results in enhancement of β-glucosidase activity .
Energy metabolism was also detected in our study. The complex network of plant energy metabolism involves photosynthesis, photorespiration, nitrogen and sulfur reduction, and other molecules . Our study identified genes affecting ATP/NADPH, such as ADP-ribose pyrophosphatase, NADH dehydrogenase, NADH/Ubiquinone/plastoquinone (complex I), and NADPH oxidase (see Additional file 15). Most of these genes also play roles in redox. The gene encoding ADP-ribose pyrophosphatase (up-regulated by 2.40-fold), conferred enhanced tolerance to oxidative stress in Arabidopsis plants, resulting from maintenance of NAD + and ATP levels by nucleotide recycling from free ADP-ribose molecules . Also, plant extracellular ATP results in the activation of plasma membrane NADPH oxidases, causing the production of reactive oxygen species . In addition, NAD(P)H dehydrogenases are related to respiratory complex I, and mediate photosystem I cyclic electron flow. Hence, we consider that energy metabolism is an aspect of the nuclear regulation of photosynthesis.
Photosynthesis and transport proteins
Transporters perform many important physiological functions, including the transport and distribution of photosynthetic assimilates. However, our study did not detect the well-known sucrose transporters, such as sucrose uptake transporters (SUTs) . This result may be caused by annotation of differentially expressed genes, which should be improved in future work. For example, MFS, a typical representative of secondary transporters and the largest known superfamily of secondary carriers found in the biosphere , was detected in our study (FC = 0.32 to 0.46). Plant sucrose transporters belong to this superfamily and can mediate carbohydrate transport across cell membranes . ABC transporters, arguably the most important family of ATP-driving transporters in biology, have been implicated in a broad range of processes, including polar auxin transport, disease resistance, and stomatal function . In a study of Butyrivibrio proteoclasticus, 12 ABC transport system substrate-binding proteins were predicted to function as carbohydrate transporters .
Transport proteins are embedded in the membrane to enable the passage of metabolites and thereby connect metabolic networks beyond organelle boundaries . Transporters may affect photosynthetic rate via metabolite transport, hormone signaling and sustaining cell homeostasis. The transport proteins we detected include phosphate transporter (FC = 0.12), PIN1-like auxin transport protein (FC = 5.37) and potassium channel KAT3 (FC = 0.31) (see Additional file 14). Transport proteins are important for achieving high rates of photosynthetic carbon assimilation [10, 82]. Also, in hormone signaling, PIN transporters (up-regulated by 5.37-, 2.97-fold) play important roles in directional auxin distribution within tissues . Recent studies have suggested that the HAK family transporters (down-regulated by 0.21-fold) are potentially involved in K+ homeostasis and osmotic regulation in plants . Also, transport plays an important role in maintaining cellular homeostasis for adaptation to environmental stress . For example, the OPT family consists of electrochemical potential–driven transporters . AtOPT6 can mediate uptake of glutathione derivatives and metal complexes, indicating that it may also be involved in redox homeostasis .
Here we report the genome-wide identification and characterization of nuclear genes involved in photosynthesis. This study detected 515 differentially expressed genes in a segregating linkage population of poplar (FC ≥ 2 or FC ≤ 0.5, P < 0.05). Our study suggests that improving photosynthetic efficiency should consider different regulatory levels, rather than just the primary reactions of carbon assimilation under field conditions. Our study also reflects a general picture of regulation of photosynthesis from the nucleus in a normal environment. This study will be a part of further analysis using systems biology, a multidisciplinary science that uses large data sets to generate hypotheses about a dynamic system and has been effectively used to study signaling networks . Identification and characterization of nuclear genes involved in photosynthesis in Populus provides new insights in the molecular mechanisms that regulate photosynthesis in field and information that may enable efforts to improve photosynthetic efficiency in trees.
Plant materials and growth condition
A total of 1200 F1 progeny, which were randomly selected from the F1 hybrid population of 5000, were used in this study. The population was established by controlled crossing between two elite poplar parents, the female hybrid clone “YX01” (P. alba × P. glandulossa) and the male clone “LM50” (P. tomentosa), two species of the section Populus. The progeny were grown in Xiao Tangshan horticulture fields of Beijing Forestry University, Beijing, China (40°2′N, 115°50′E), using a randomized complete block design with three replications in 2008.
Measurement of photosynthetic characteristics and quantitative traits
Photosynthetic characteristics were measured from fully expanded leaves using the LI-6400 portable photosynthesis system (Li-Cor Inc., Lincoln, NE, USA) at 9:00–11:00 on sunny days from July 20th to August 8th, 2010. Growing conditions during the experimental time window are shown in Additional file 21: Table S9. Three functional leaves, the fourth to sixth counting from the individual stem head of all of the individuals, were measured with three replications for each leaf. Values of photosynthetic parameters, such as Pn, Cond and Ci, were automatically recorded when Pn showed no systematic decrease or increase (± 0.1). Besides, seven quantitative traits including H, D (1.3 m above the ground), V, MFA and holocellulose, α-cellulose, and lignin contents were measured in all three replicates of the 1,200 clones in the hybrid population described by Du et al. (2013) . Broad-sense heritability was calculated as in Singh et al. (1993) .
Bulk segregant analysis and RNA extraction
According to the average value of each individual for 1200 progeny, fifty individuals with values distributed in the extreme area were measured again to ensure the stable phenotypic variance in photosynthetic characteristics. Among them, fifteen individuals with high (Pn > 21.000 μmol•m−2•s−1) and fifteen individuals of low photosynthetic rate (Pn < 11.000 μmol•m−2•s−1) were selected to construct gene pools by BSA according to Michelmore et al. (1991) , to produce two pooled samples with genetically dissimilar photosynthetic rates. All leaf samples were immediately placed into liquid nitrogen in the field and stored at −80°C until used for isolating RNA. Samples were segregated into two groups (high and low) and five individuals were pooled, producing three biological repeats for each group. These high Pn groups were named High1, High2, High3. And low Pn groups were named Low1, Low2, Low3. A simple t-test using the Statistic Package for Social Science (SPSS) among these pools showed a significant difference between high and low photosynthetic rate groups (Additional file 22: Table S10) (P ≤ 0.01). Total RNA was extracted using the Plant Qiagen RNAeasy kit (Qiagen China, Shanghai) according to the manufacturer’s instructions. RNA extractions of 5 individuals were mixed in each replicate to equal quantities (2 mg) for later microarray analysis. All the RNA samples (individual and mixed) were examined by Agilent 2100 Bioanalyzer (Agilent Technologies, USA) according to the manufacturer’s instructions, and no evidence of degradation was noted. The RNA samples were reverse transcribed into cDNA using the SuperScript First-Strand Synthesis system and the supplied polythymine primers (Invitrogen). In total, six gene pools were constructed, representing samples with three high and three low photosynthetic rates, respectively.
Array hybridization and washes were performed using the GeneChip Hybridization, Wash and Stain Kit (cat. #900720; Affymetrix, Santa Clara, CA) in a Hybridization Oven 645 (cat. #00-0331-220 V; Affymetrix) and Fluidics Station 450 (cat. #00-0079; Affymetrix) following the manufacturer’s instructions. The array contains 61,251 poplar probe sets (including seven rRNA probe sets), 12 poplar control probe sets, and 62 reporter probe sets. Slides were scanned by GeneChip Scanner 3000 (cat. #00-00212; Affymetrix) and Command Console Software 3.1 (Affymetrix) with default settings. Raw data were normalized via the MAS 5.0 algorithm, Gene Spring Software 11.0 (Agilent Technologies). Due to the high technical consistency and reliability of microarrays, technical replications of hybridizations were not performed. cRNA labeling and hybridization to the Poplar Genome Array were performed by the ShanghaiBio Corporation in China. The expression data of all samples were uploaded to the Gene Expression Omnibus (http://www.ncbi.nlm.nih.gov/geo/) with accession number GSE47105.
Quantitative real-time PCR validation of expression profiles
Quantitative PCR was performed on a DNA Engine Opticon 2 machine (MJ Research) using the LightCycler-FastStar DNA master SYBR Green I kit (Roche). The PCR program was described in Zhang et al. . The melting curve was used to check the specificity of the amplified fragments. All reactions were carried out in triplicate for biological repeats, and the real-time data were analyzed using the Opticon Monitor Analysis Software 3.1 tool. Specific primer sets were designed for each gene using Primer Express 3.0 software (Applied Biosystems) (Additional file 6: Table S3). The efficiency of the primer sets was calculated by performing real-time PCR on several dilutions of first-strand cDNAs. Efficiencies of the different primer sets were similar. The specificity of each primer set was checked by sequencing PCR products. The results obtained for the different samples were standardized to the levels of Actin.
Biological interpretation and cluster analysis
Gene annotations were obtained from GenBank (http://www.ncbi.nlm.nih.gov/genbank/), JGI (http://www.phytozome.net/poplar), PopGenie v2.0 (http://popgenie.org/flashbulktools) and TAIR (http://www.arabidopsis.org/). CateGOrizer (http://www.animalgenome.org/tools/catego/) was used for GO Term classification. We categorized differentially expressed genes by their Gene Ontology class using SEA, which was performed on AgriGO (http://bioinfo.cau.edu.cn/agriGO/) to identify the significantly enriched biological processes, cellular components and molecular functions. Complete-linkage hierarchical clustering was done using SAS for the expression pattern of specific genes at the SBS server of Ebioservice (http://www.ebioservice.com/).
DNA extraction, SNP discovery, genotyping and single-marker analysis
Total genomic DNA was isolated from young leaves using a DNeasy Plant Mini Kit (Qiagen China, Shanghai) following the manufacturer’s protocol. To determine the SNP loci segregating in the F1 population of “YX01” × “LM50”, the genomic sequences of six candidate genes, i.e. XET, Dabb, GASA, SAUR, CGSS, and PI, were identified from the parents. The primer sets of these candidate genes used for the amplification were designed based on the P. trichocarpa genome sequence. In total, 96 sequences of candidate genes (6 genes × 8 YX01, 6 genes × 8 LM50) were obtained by sequencing the female hybrid clone “YX01” (P. alba × P. glandulossa) and the male clone “LM50” (P. tomentosa). After re-sequencing, Sequencher v.4.0 and BioEdit were used for sequence alignment and manual editing was used to confirm sequence quality and remove primer sequences. Diploid sequences were disambiguated into haplotypes using Phase v. 2.1 using 10,000 iterations of the Bayesian MCMC chain (Stephens and Scheet 2005). Subsequently, SNP discovery was performed with MEGA 4.0. The sequence data from this article has been deposited in the GenBank Data Library under the accession Nos. JX431909-JX431932. In total, 300 individuals of 1200 progeny were randomly selected for genotyping and single-marker analysis. 158 common SNPs (Minor Allele Frequency > 0.10) were genotyped in this association population by using locked nucleic acid technology . Single-marker analysis based on the SNP markers and 11 traits was performed in the F1 hybrid population using single factor ANOVA. Percent phenotypic variance explained by the most significant marker was calculated, and the positive FDR with 104 permutations was used to perform a correction for multiple testing in QVALUE (Storey and Tibshirani 2003) .
This work was supported by grants from the State Key Basic Research Program of China (No. 2012CB114506), the 111 Project (No. B13007), and the Project of the National Natural Science Foundation of China (No. 31170622, 30872042). We also would like to thank Dr. Yuhua Cui (Michigan State University), Dr. Yuepeng Song (Beijing Forest University) and Yafei Lv (Beijing Forest University) for helpful suggestions for data analysis.
- Whitney SM, Houtz RL, Alonso H: Advancing our understanding and capacity to engineer nature’s CO2-sequestering enzyme, rubisco. Plant Physiol. 2011, 155: 27-35. 10.1104/pp.110.164814.PubMed CentralView ArticlePubMedGoogle Scholar
- Evans JR, Caemmerer SV: Enhancing photosynthesis. Plant Physiol. 2011, 155: 19-10.1104/pp.110.900402.PubMed CentralView ArticlePubMedGoogle Scholar
- Makino A: Photosynthesis, grain yield, and nitrogen utilization in rice and wheat. Plant Physiol. 2011, 155: 125-129. 10.1104/pp.110.165076.PubMed CentralView ArticlePubMedGoogle Scholar
- Schlesinger WH, Lichter J: Limited carbon storage in soil and litter of experimental forest plots under increased atmospheric CO2. Nature. 2001, 411: 466-469. 10.1038/35078060.View ArticlePubMedGoogle Scholar
- Li L, Lu S, Chiang V: A genomic and molecular view of wood formation. Crit Rev in Plant Sci. 2006, 25: 213-233.View ArticleGoogle Scholar
- Kirschbaum MUF: Does enhanced photosynthesis enhance growth? Lessons learned from CO2 enrichment studies. Plant Physiol. 2011, 155: 117-124. 10.1104/pp.110.166819.PubMed CentralView ArticlePubMedGoogle Scholar
- Murchie EH, Pinto M, Horton P: Agriculture and the new challenges for photosynthesis research. New Phytol. 2009, 181: 352-552.View ArticleGoogle Scholar
- Peterhansel C, Maurino VG: Photorespiration redesigned. Plant Physiol. 2011, 155: 49-55. 10.1104/pp.110.165019.PubMed CentralView ArticlePubMedGoogle Scholar
- Gowik U, Westhoff P: The path from C3 to C4 photosynthesis. Plant Physiol. 2011, 155: 56-63. 10.1104/pp.110.165308.PubMed CentralView ArticlePubMedGoogle Scholar
- Bräutigam A, Weber APM: Do metabolite transport processes limit photosynthesis?. Plant Physiol. 2011, 155: 43-48. 10.1104/pp.110.164970.PubMed CentralView ArticlePubMedGoogle Scholar
- Pesaresi P, Schneider A, Kleine T, Leister D: Interorganellar communication. Curr Opin Plant Biol. 2007, 10: 600-606. 10.1016/j.pbi.2007.07.007.View ArticlePubMedGoogle Scholar
- 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.View ArticlePubMedGoogle Scholar
- Woodson JD, Chory J: Coordination of gene expression between organellar and nuclear genomes. Nat Rev Genet. 2008, 9: 383-395. 10.1038/nrg2348.View ArticlePubMedGoogle Scholar
- Hohmann-Marriott MF, Blankenship RE: Evolution of photosynthesis. Annu Rev Plant Biol. 2011, 62: 515-548. 10.1146/annurev-arplant-042110-103811.View ArticlePubMedGoogle Scholar
- Ferro M, Brugière S, Salvi D, Seigneurin-Berny D, Court M, Moyet L, Ramus C, Miras S, Mellal M, Le Gall S, Kieffer-Jaquinod S, Bruley C, Garin J, Joyard J, Masselon C, Rolland N: AT_CHLORO, a comprehensive chloroplast proteome database with subplastidial localization and curated information on envelope proteins. Mol Cell Proteomics. 2010, 9: 1063-1084. 10.1074/mcp.M900325-MCP200.PubMed CentralView ArticlePubMedGoogle Scholar
- Bruley C, Dupierris V, Salvi D, Rolland N, Ferro M: AT_CHLORO: a chloroplast protein database dedicated to sub-plastidial localization. Front Plant Sci. 2012, 3: 1-8.View ArticleGoogle Scholar
- Richly E, Dietzmann A, Biehl A, Kurth J, Laloi C, Apel K, Salamini F, Leister D: Covariations in the nucleus chloroplast transcriptome reveal a regulatory master-switch. EMBO reports. 2003, 4: 491-498. 10.1038/sj.embor.embor828.PubMed CentralView ArticlePubMedGoogle Scholar
- Jung HS, Chory J: Signaling between chloroplasts and nucleus: can a systems biology approach bring clarity to a complex and highly regulated pathway?. Plant Physiol. 2010, 152: 453-459. 10.1104/pp.109.149070.PubMed CentralView ArticlePubMedGoogle Scholar
- Parry MAJ, Madgwick PJ, Carvalho JFC, Andralojc PJ: Prospects for increasing photosynthesis by overcoming the limitations of rubisco. J Agric Sci. 2007, 145: 31-43. 10.1017/S0021859606006666.View ArticleGoogle Scholar
- Nishimura K, Ogawa T, Ashida H, Yokota A: Molecular mechanisms of rubisco biosynthesis in higher plants. Plant Biotechnol. 2008, 25: 285-290. 10.5511/plantbiotechnology.25.285.View ArticleGoogle Scholar
- Mao YS, Zhang B, Spector DL: Biogenesis and function of nuclear bodies. Trends Genet. 2011, 27: 295-306. 10.1016/j.tig.2011.05.006.PubMed CentralView ArticlePubMedGoogle Scholar
- Terashima I, Hanba YT, Tholen D, Niinemets Ü: Leaf functional anatomy in relation to photosynthesis. Plant Physiol. 2011, 155: 108-116. 10.1104/pp.110.165472.PubMed CentralView ArticlePubMedGoogle Scholar
- Murchie EH, Niyogi KK: Manipulation of photoprotection to improve plant photosynthesis. Plant Physiol. 2011, 155: 86-92. 10.1104/pp.110.168831.PubMed CentralView ArticlePubMedGoogle Scholar
- Kramer DM, Evans JR: The importance of energy balance in improving photosynthetic productivity. Plant Physiol. 2011, 155: 70-78. 10.1104/pp.110.166652.PubMed CentralView ArticlePubMedGoogle Scholar
- Foyer CH, Shigeoka S: Understanding oxidative stress and antioxidant functions to enhance photosynthesis. Plant Physiol. 2011, 155: 93-100. 10.1104/pp.110.166181.PubMed CentralView ArticlePubMedGoogle Scholar
- Bilgin DD, Zavala JA, Zhu J, Clough SJ, Donald R, DeLucia EH: Biotic stress globally downregulates photosynthesis genes. Plant Cell Environ. 2010, 33: 1597-1613. 10.1111/j.1365-3040.2010.02167.x.View ArticlePubMedGoogle Scholar
- Song Y, Chen Q, Ci D, Zhang D: Transcriptome profiling reveals differential transcript abundance in response to chilling stress in Populus simonii. Plant Cell Rep. 2013, 32: 1407-1425. 10.1007/s00299-013-1454-x.View ArticlePubMedGoogle Scholar
- Pereira MVJS, Gazarini LC, David TS, David JS, Rodrigues A, Maroco J, Chaves MM: Drought-induced photosynthetic inhibition and autumn recovery in two Mediterranean oak species (Quercus ilex and Quercus suber). Tree Physiol. 2010, 30: 946-956. 10.1093/treephys/tpq044.View ArticlePubMedGoogle Scholar
- Chaves MM, Flexas J, Pinheiro C: Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot. 2009, 103: 551-560.PubMed CentralView ArticlePubMedGoogle Scholar
- Magnani F, Mencuccini M, Borghetti M, Berbigier P, Berninger F, Delzon S, Grelle A, Hari P, Javis PG, Andrew PK, Kowalski S, Lankreijer H, Law BE, Lindroth A, Loustau D, Manca G, Moncrieff HB, Rayment M, Tedeschi V, Valentini R, Grace J: The human footprint in the carbon cycle of temperate and boreal forests. Nature. 2007, 447: 849-851. 10.1038/nature05847.View ArticleGoogle Scholar
- Ayre BG: Membrane-transport systems for sucrose in relation to whole-plant carbon partitioning. Mol Plant. 2011, 4: 377-394. 10.1093/mp/ssr014.View ArticlePubMedGoogle Scholar
- Jansson S, Douglas CJ: Populus: a model system for plant biology. Annu Rev Plant Biol. 2007, 58: 435-458. 10.1146/annurev.arplant.58.032806.103956.View ArticlePubMedGoogle Scholar
- Tuskan GA, DiFazio S, Jansson S, Bohlmann J, Grigoriev I, Hellsten U, Putnam N, Ralph S, Rombauts S, Salamov S, Schein J, Sterck L, Aerts A, Bhalerao RR, Bhalerao RP, Blaudez D, Boerjan W, Brun A, Brunner A, Busov V, Campbell M, Carlson J, Chalot M, Chapman J, Chen GL, Cooper D, Coutinho PM, Couturier J, Covert S, Cronk Q, et al: The genome of black cottonwood, Populus trichocarpa (Torr. & Gray). Science. 2006, 313: 1596-1604. 10.1126/science.1128691.View ArticlePubMedGoogle Scholar
- Strauss SH, Martin FM: Poplar genomics comes of age. New Phytol. 2004, 164: 1-4. 10.1111/j.1469-8137.2004.01179.x.View ArticleGoogle Scholar
- Michelmore RW, Paran I, Kesseli RV: Identification of markers linked to disease-resistance genes by bulked segregant analysis: A rapid method to detect markers in specific genomic regions by using segregating populations. Proc Natl Acad SciUSA. 1991, 88: 9828-9832. 10.1073/pnas.88.21.9828.View ArticleGoogle Scholar
- Thimm O, Bläsing O, Gibon Y, Nagel A, Meyer S, Krüger P, Selbig J, Müller LA, Rhee SY, Stitt M: MapMan: a user-driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes. Plant J. 2004, 37: 914-939. 10.1111/j.1365-313X.2004.02016.x.View ArticlePubMedGoogle Scholar
- Neale DB, Savolainen O: Association genetics of complex traits in conifers. Trends Plant Sci. 2004, 9: 325-330. 10.1016/j.tplants.2004.05.006.View ArticlePubMedGoogle Scholar
- Misra P, Pandey A, Tiwari M, Chandrashekar K, Sidhu OP, Asif MH, Chakrabarty D, Singh PK, Trivedi PK, Nath P, Tuli R: Modulation of transcriptome and metabolome of tobacco by Arabidopsis transcription factor, AtMYB12, leads to insect resistance. Plant Physiol. 2010, 152: 2258-2268. 10.1104/pp.109.150979.PubMed CentralView ArticlePubMedGoogle Scholar
- Geisler K, Hughes RK, Sainsbury F, Lomonossoff GP, Rejzek M, Fairhurst S, Olsen CK, Motawia MS, Melton RE, Hemmings AM, Bak S, Osbourn A: Biochemical analysis of a multifunctional cytochrome P450 (CYP51) enzyme required for synthesis of antimicrobial triterpenes in plants. Proc Natl Acad Sci U S A. 2013, 110: 3360-3367. 10.1073/pnas.1309157110.View ArticleGoogle Scholar
- Yoshida K, Terashima I, Noguchi K: Distinct roles of the cytochrome pathway and alternative oxidase in leaf photosynthesis. Plant Cell Physiol. 2006, 47: 22-31.View ArticlePubMedGoogle Scholar
- Yoshida K, Terashima I, Noguchi K: Up-regulation of mitochondrial alternative oxidase concomitant with chloroplast over-reduction by excess light. Plant Cell Physiol. 2007, 48: 606-614. 10.1093/pcp/pcm033.View ArticlePubMedGoogle Scholar
- Sjögren LLE, Clarke AK: Assembly of the chloroplast ATP-dependent Clp protease in Arabidopsis is regulated by the ClpT accessory proteins. Plant Cell. 2011, 23: 322-332. 10.1105/tpc.110.082321.PubMed CentralView ArticlePubMedGoogle Scholar
- Biehl A, Richly E, Noutsos C, Salamini F, Leister D: Analysis of 101 nuclear transcriptomes reveals 23 distinct regulons and their relationship to metabolism, chromosomal gene distribution and co-ordination of nuclear and plastid gene expression. Gene. 2005, 344: 33-41.View ArticlePubMedGoogle Scholar
- Mellerowicz EJ, Sundberg B: Wood cell walls: biosynthesis, developmental dynamics and their implications for wood properties. Curr Opin Plant Biol. 2008, 11: 293-300. 10.1016/j.pbi.2008.03.003.View ArticlePubMedGoogle Scholar
- Geisler-Lee J, Geisler M, Coutinho PM, Segerman B, Nishikubo N, Takahashi J, Aspeborg H, Djerbi S, Master E, Gunnerås SA, Sundberg B, Karpinski S, Teeri TT, Kleczkowski LA, Henrissat B, Mellerowicz EJ: Poplar carbohydrate-active enzymes. Gene identification and expression analyses. Plant Physiol. 2006, 140: 946-962. 10.1104/pp.105.072652.PubMed CentralView ArticlePubMedGoogle Scholar
- Cosgrove DJ: Growth of the plant cell wall. Nat Rev. 2005, 6: 850-861.View ArticleGoogle Scholar
- Pelloux J, Rustérucci C, Mellerowicz EJ: New insights into pectin methylesterase structure and function. Trends Plant Sci. 2007, 12: 267-277. 10.1016/j.tplants.2007.04.001.View ArticlePubMedGoogle Scholar
- Micheli F, Sundberg B, Goldberg R, Richard L: Radial distribution pattern of pectin methylesterases across the cambial region of hybrid aspen at activity and dormancy. Plant Physiol. 2000, 124: 191-199. 10.1104/pp.124.1.191.PubMed CentralView ArticlePubMedGoogle Scholar
- Hayashi T, Kaida R: Functions of xyloglucan in plant cells. Mol Plant. 2011, 4: 17-24. 10.1093/mp/ssq063.View ArticlePubMedGoogle Scholar
- Rolland F, Baena-Gonzalez E, Sheen J: Sugar sensing and signaling in plants: conserved and novel mechanisms. Annu Rev Plant Biol. 2006, 57: 675-709. 10.1146/annurev.arplant.57.032905.105441.View ArticlePubMedGoogle Scholar
- Nishikubo N, Takahashi J, Roos AA, Maceluch MD, Piens K, Brumer H, Teeri TT, Stålbrand H, Mellerowicz EJ: Xyloglucan endo-transglycosylase-mediated xyloglucan rearrangements in developing wood of hybrid aspen. Plant Physiol. 2011, 155: 399-413. 10.1104/pp.110.166934.PubMed CentralView ArticlePubMedGoogle Scholar
- Anita G: Plant chitinases: Genetic diversity and physiological roles. CRIT Rev Plant Sci. 2012, 31: 57-73. 10.1080/07352689.2011.616043.View ArticleGoogle Scholar
- Kiba A, Nishihara M, Nakatsuka T, Yamamura S: Pathogenesis-related protein 1 homologue is an antifungal protein in Wasabia japonica leaves and confers resistance to Botrytis cinerea in transgenic tobacco. Plant Biotechnol J. 2007, 24: 247-253. 10.5511/plantbiotechnology.24.247.View ArticleGoogle Scholar
- Sels J, Mathys J, De Coninck BM, Cammue BP, De Bolle MF: Plant pathogenesis-related (PR) proteins: a focus on PR peptides. Plant Physiol Biochem. 2008, 46: 941-950. 10.1016/j.plaphy.2008.06.011.View ArticlePubMedGoogle Scholar
- Ryan MJ, Yoder BJ: Hydraulic limits to tree height and tree growth. Bioscience. 1997, 47: 235-242. 10.2307/1313077.View ArticleGoogle Scholar
- Yamaguchi M, Valliyodan B, Zhang J, Lenoble ME, Yu O, Elizabeth ER, Nguyen HT, Sharp RE: Regulation of growth response to water stress in the soybean primary root. I. Proteomic analysis reveals region-specific regulation of phenylpropanoid metabolism and control of free iron in the elongation zone. Plant Cell Environ. 2010, 33: 223-243. 10.1111/j.1365-3040.2009.02073.x.View ArticlePubMedGoogle Scholar
- Spollen WG, Tao W, Valliyodan B, Chen K, Hejlek LJ, Kim JJ, Noble MEL, Zhu J, Bohnert HJ, Henderson D, Schachtman DP, Davis GE, Springer GK, Sharp RE, Nguyen HT: Spatial distribution of transcript changes in the maize primary root elongation zone at low water potential. BMC Plant Biol. 2008, 8: 32-10.1186/1471-2229-8-32.PubMed CentralView ArticlePubMedGoogle Scholar
- Santner A, Estelle M: Recent advances and emerging trends in plant hormone signaling. Nature. 2009, 459: 1071-1078. 10.1038/nature08122.View ArticlePubMedGoogle Scholar
- Blilou I, Xu J, Wildwater M, Willemsen V, Paponov I, Friml J, Heidstra R, Aida M, Palme K, Scheres B: The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots. Nature. 2005, 433: 39-44. 10.1038/nature03184.View ArticlePubMedGoogle Scholar
- Iqbal N, Nazar R, Khan MIR, Masood A, Khan NA: Role of gibberellins in regulation of source-sink relations under optimal and limiting environmental conditions. Current Sci. 2011, 100: 998-1007.Google Scholar
- Yuan L, Xu DQ: Stimulation effect of gibberellic acid short-term treatment on leaf photosynthesis related to the increase in rubisco content in broad bean and soybean. Photosynth Res. 2001, 68: 39-47. 10.1023/A:1011894912421.View ArticlePubMedGoogle Scholar
- Zhang Y, Liu Z, Liu R, Wang L, Bi Y: Gibberellins negatively regulate light-induced nitrate reductase activity in Arabidopsis seedlings. J Plant physiol. 2011, 168: 2161-2168. 10.1016/j.jplph.2011.07.004.View ArticlePubMedGoogle Scholar
- Ribeiro DM, Araújo WL, Fernie AR, Schippers JHM, Roeber BM: Action of gibberellins on growth and metabolism of Arabidopsis plants associated with high concentration of carbon dioxide. Plant physiol. 2012, 160: 1781-1794. 10.1104/pp.112.204842.PubMed CentralView ArticlePubMedGoogle Scholar
- Komatsu S, Zang X, Tanaka N: Comparison of two proteomics techniques used to identify proteins regulated by gibberellin in rice. J Proteome Res. 2006, 5: 270-276. 10.1021/pr0502929.View ArticlePubMedGoogle Scholar
- Lamkemeyer P, Laxa M, Collin V, Li W, Finkemeier I, Schöttler MA, Holtkamp V, Tognetti VB, Bourguet EI, Kandlbinder A, Weis E, Maslow MM, Dietz KJ: Peroxiredoxin Q of Arabidopsis thaliana is attached to the thylakoids and functions in context of photosynthesis. Plant J. 2006, 45: 968-981. 10.1111/j.1365-313X.2006.02665.x.View ArticlePubMedGoogle Scholar
- Ort DR: When there is too much light. Plant Physiol. 2001, 2001 (125): 29-32.View ArticleGoogle Scholar
- Chen L, Song Y, Li S, Zhang L, Zou C, Yu D: The role of WRKY transcription factors in plant abiotic stresses. Biochim Biophys Acta. 2012, 1819 (2): 120-128. 10.1016/j.bbagrm.2011.09.002.View ArticlePubMedGoogle Scholar
- Hadrami AE, Adam LR, Hadrami IE, Daayf F: Chitosan in plant protection. Mar Drugs. 2010, 8: 968-987. 10.3390/md8040968.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang W, Vinocur B, Shoseyov O, Altman A: Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004, 9: 244-252. 10.1016/j.tplants.2004.03.006.View ArticlePubMedGoogle Scholar
- Hiraga S, Sasaki K, Ohashi Y, Matsui H: A large family of class III plant peroxidases. Plant Cell Physiol. 2001, 42: 462-468. 10.1093/pcp/pce061.View ArticlePubMedGoogle Scholar
- Finkemeier I, Goodman M, Lamkemeyer P, Kandlbinder A, Sweet-love LJ, Dietz KJ: The mitochondrial type II peroxiredoxin F is essential for redox homeostasis and root growth of Arabidopsis thaliana under stress. J Biol Chem. 2005, 280: 12168-12180. 10.1074/jbc.M413189200.View ArticlePubMedGoogle Scholar
- Biswal B, Joshi PN, Raval MK, Biswal UC: Photosynthesis, a global sensor of environmental stress in green plants: stress signalling and adaptation. Curr Sci. 2011, 101: 47-56.Google Scholar
- Mohapatra PK, Patro L, Raval MK, Ramaswamy NK, Biswal UC, Biswal B: Senescence-induced loss in photosynthesis enhances cell wall β-glucosidase activity. Physiol Plantarum. 2010, 138: 346-355. 10.1111/j.1399-3054.2009.01327.x.View ArticleGoogle Scholar
- Ogawa T, Ishikawa K, Harada K, Fukusaki E, Yoshimura K, Shigeoka S: Overexpression of an ADP-ribose pyrophosphatase, AtNUDX2, confers enhanced tolerance to oxidative stress in Arabidopsis plants. The Plant J. 2009, 57: 289-301. 10.1111/j.1365-313X.2008.03686.x.View ArticlePubMedGoogle Scholar
- Demidchik V, Shang Z, Shin R, Thompson E, Rubio L, Laohavisit A, Mortimer JC, Chivasa S, Slabas AR, Glover BJ, Schachtman DP, Shabala SN, Davies JM: Plant extracellular ATP signalling by plasma membrane NADPH oxidase and Ca2+channels. The Plant J. 2009, 58: 903-913. 10.1111/j.1365-313X.2009.03830.x.View ArticlePubMedGoogle Scholar
- Kühn C, Grof CPL: Sucrose transporters of higher plants. Curr Opin Plant Biol. 2010, 13: 288-298.View ArticlePubMedGoogle Scholar
- Reddy VS, Shlykov MA, Castillo R, Sun EI, Saier MH: The major facilitator superfamily (MFS) revisited. FEBS J. 2012, 279: 2022-2035. 10.1111/j.1742-4658.2012.08588.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Niederholtmeyer H, Wolfstadter BT, Savage DF, Silver PA, Way JC: Engineering cyanobacteria to synthesize and export hydrophilic products. Appl Environ Microbiol. 2010, 76: 3462-3466. 10.1128/AEM.00202-10.PubMed CentralView ArticlePubMedGoogle Scholar
- Rea PA: Plant ATP-Binding cassette transporters. Annu Rev Plant Biol. 2007, 58: 347-375. 10.1146/annurev.arplant.57.032905.105406.View ArticlePubMedGoogle Scholar
- Bond J, Dunne JC, Kwan FYS, Li D, Zhang K, Leahy SC, Kelly WJ, Attwood GT, Jordan TW: Carbohydrate transporting membrane proteins of the rumen bacterium, Butyrivibrio proteoclasticus. J Proteomics. 2012, 75: 3138-3144. 10.1016/j.jprot.2011.12.013.View ArticlePubMedGoogle Scholar
- Linka N, Weber APM: Intracellular metabolite transporters in plants. Mol Plant. 2010, 3: 21-53. 10.1093/mp/ssp108.View ArticlePubMedGoogle Scholar
- Bräutigam A, Hoffmann-Benning S, Weber AP: Comparative proteomics of chloroplast envelopes from C3 and C4 plants reveals specific adaptations of the plastid envelope to C4 photosynthesis and candidate proteins required for maintaining C4 metabolite fluxes. Plant Physiol. 2008, 148: 568-579. 10.1104/pp.108.121012.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang J, Nodzyňski T, Pěnčík A, Rolčík J, Friml J: PIN phosphorylation is sufficient to mediate PIN polarity and direct auxin transport. Proc Natl Acad Sci U S A. 2010, 107: 918-922. 10.1073/pnas.0909460107.PubMed CentralView ArticlePubMedGoogle Scholar
- Osakabe Y, Arinaga N, Umezawa T, Katsura S, Nagamachi K, Tanaka H, Ohiraki H, Yamada K, Seo S, Abo M, Yoshimura E, Shinozaki K, Shinozaki KY: Osmotic stress responses and plant growth controlled by potassium transporters in Arabidopsis. Plant Cell. 2013, 25: 609-624. 10.1105/tpc.112.105700.PubMed CentralView ArticlePubMedGoogle Scholar
- Conde A, Chaves MM, Gerós H: Membrane transport, sensing and signaling in plant adaptation to environmental stress. Plant Cell Physiol. 2011, 52: 1583-1602. 10.1093/pcp/pcr107.View ArticlePubMedGoogle Scholar
- Gomolplitinant KM, Saier MH: Evolution of the oligopeptide transporter family. J Membr Biol. 2011, 240: 89-110. 10.1007/s00232-011-9347-9.PubMed CentralView ArticlePubMedGoogle Scholar
- Cagnac O, Bourbouloux A, Chakrabarty D, Zhang MY, Delrot S: AtOPT6 transports glutathione derivatives and is induced by primisulfuron. Plant Physiol. 2004, 135: 1378-1387. 10.1104/pp.104.039859.PubMed CentralView ArticlePubMedGoogle Scholar
- Du QZ, Pan W, Xu BH, Li BL, Zhang DQ: Polymorphic SSR loci within PtoCesA genes are associated with growth and wood properties in Populus tomentosa. New Phytol. 2013, 197: 763-776. 10.1111/nph.12072.View ArticlePubMedGoogle Scholar
- Singh M, Ceccarelli S, Hamblin J: Estimation of heritability from varietal trial data. Theor Appl Genet. 1993, 86: 437-441. 10.1007/BF00838558.View ArticlePubMedGoogle Scholar
- Zhang DQ, Xu BH, Yang XH, Zhang ZY, Li BL: The sucrose synthase gene family in Populus: structure, expression, and evolution. Tree Genet Genomes. 2001, 7: 443-456.View ArticleGoogle Scholar
- Koshkin AA, Singh SK, Nielsen P, Rajwanshi VK, Meldgaard KRM, Olsen CE, Wengel J: LNA (locked nucleic acids): synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligo merisation, and unprecendented nucleic acid recognition. Tetrahedron. 1998, 54: 3607-3630. 10.1016/S0040-4020(98)00094-5.View ArticleGoogle Scholar
- Storey JD, Tibshirani R: Statistical significance for genomewide studies. Proc Natl Acad Sci. 2003, 100: 9440-9445. 10.1073/pnas.1530509100.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.