- Research article
- Open Access
PnTgs1-like expression during reproductive development supports a role for RNA methyltransferases in the aposporous pathway
© Siena et al.; licensee BioMed Central Ltd. 2014
- Received: 5 April 2014
- Accepted: 20 October 2014
- Published: 18 November 2014
In flowering plants, apomixis (asexual reproduction via seeds) is widely believed to result from failure of key regulators of the sexual female reproductive pathway. In the past few years, both differential display and RNA-seq comparative approaches involving reproductive organs of sexual plants and their apomictic counterparts have yielded extensive lists of candidate genes. Nevertheless, only a limited number of these genes have been functionally characterized, with few clues consequently available for understanding the molecular control of apomixis. We have previously identified several cDNA fragments with high similarity to genes involved in RNA biology and with differential amplification between sexual and apomictic Paspalum notatum plants. Here, we report the characterization of one of these candidates, namely, N69 encoding a protein of the S-adenosyl-L-methionine-dependent methyltransferases superfamily. The purpose of this work was to extend the N69 cDNA sequence and to characterize its expression at different developmental stages in both sexual and apomictic individuals.
Molecular characterization of the N69 cDNA revealed homology with genes encoding proteins similar to yeast and mammalian trimethylguanosine synthase/PRIP-interacting proteins. These proteins play a dual role as ERK2-controlled transcriptional coactivators and mediators of sn(o)RNA and telomerase RNA cap trimethylation, and participate in mammals and yeast development. The N69-extended sequence was consequently renamed PnTgs1-like. Expression of PnTgs1-like during reproductive development was significantly higher in floral organs of sexual genotypes compared with apomicts. This difference was not detected in vegetative tissues. In addition, expression levels in reproductive tissues of several genotypes were negatively correlated with facultative apomixis rates. Moreover, in situ hybridization observations revealed that PnTgs1-like expression is relatively higher in ovules of sexual plants throughout development, from premeiosis to maturity. Tissues where differential expression is detected include nucellar cells, the site of aposporous initials differentiation in apomictic genotypes.
Our results indicate that PnTgs1-like (formerly N69) encodes a trimethylguanosine synthase-like protein whose function in mammals and yeast is critical for development, including reproduction. Our findings also suggest a pivotal role for this candidate gene in nucellar cell fate, as its diminished expression is correlated with initiation of the apomictic pathway in plants.
- Gene expression
- RNA processing
- Trimethylguanosine synthase
Gametophytic apomixis in flowering plants refers to asexual reproduction through seeds . This reproductive mode can be achieved through diverse paths  and is widespread in angiosperms . With two major distinctions, the developmental programs governing plant sexuality typically form the basis of apomixis. The first important difference involves differentiation of one or more functional unreduced female gametophytes, which occurs within the nucellus after either meiosis failure (diplosporous type) or nucellar cell fate alteration (aposporous type). Second, female gamete fertilization is not required for seed formation, leading to the development of a maternal embryo by parthenogenesis. The endosperm originates autonomously or after fertilization of the polar nuclei (pseudogamy).
Paspalum , one of the largest genera within Poaceae (Gramineae), encompasses approximately 370 species classified into four subgenera (Anachyris, Ceresia, Harpostachys, and Paspalum sensu stricto) (reviewed in ). Paspalum notatum is a member of the subgenus Paspalum and forms an agamic complex comprising self-sterile sexual diploids and self-fertile apomictic autotetraploids . Paspalum notatum apomictic genotypes reproduce through apospory. In immature ovules at the premeiotic stage, one to several companion nucellar cells surrounding the megaspore mother cell enlarge, undergo a series of mitoses, and finally differentiate into non-reduced embryo sacs termed aposporous embryo sacs (AESs). AESs may coexist with the single meiotically-derived embryo sac (MES), or alternatively outcompete it and occupy the entire volume of the mature ovule . The structure of a Paspalum notatum MES is typical of Gramineae species: one egg cell, two synergids, one bi-nucleated central cell, and a mass of proliferating antipodals . On the other hand, AESs exhibit a distinct pentanucleate morphological structure (Paspalum-type embryo sacs) characterized by the presence of one egg cell, two synergids, and one bi-nucleated central cell but no antipodals; this structure allows straightforward classification by cytoembryological analysis of clarified ovules . At anthesis, MESs undergo typical angiosperm double fertilization to produce viable seeds. In contrast, AESs usually develop into seeds after fertilization of the central cell with parthenogenetic embryo formation (pseudogamy). Nearly 100% of ovules of obligate aposporous individuals contain only AESs, whereas facultative aposporous individuals display variable proportions of mature mixed ovules that include both a MES and one or more AES. Although fully sexual polyploid individuals do not exist in nature, some genotypes have been produced artificially through colchicine-induced chromosome doubling of sexual diploids  or by crossing facultative apomicts .
Apomixis in Paspalum notatum is inherited as a dominant, monogenic trait, with a distorted segregation ratio, and is associated with a single genomic region, the Apospory Controlling Region (ACR) ,-. Mapping approaches have revealed strong suppression of recombination within the Paspalum notatum ACR and disomic inheritance, whereas the remaining genomic regions show polysomic inheritance ,. Partial resolution of the ACR has unveiled a rather complex genomic structure comprising genomic sectors syntenic to rice chromosomes 2 and 12 but extensively rearranged through inversion, translocation, and/or insertion of low- and high-copy number retroelements ,,-. These features are strongly consistent with the lack of recombination detected by genetic mapping and the distorted segregation ratios against apospory observed in some progenies. Whether the peculiar ACR genomic structure is pivotal to the transcriptomic changes required to switch from sexuality to apospory is nevertheless unknown. Interestingly, our current knowledge suggests that although gene-poor, the ACR contains several sequences putatively encoding proteins, including an MT-A70-like candidate (mRNA N6-adenosine-methyltransferase) . This enzyme catalyzes N6-adenosine methylation in nascent mRNA and plays key roles in cell fate decision in multiple eukaryote systems . In particular, MT-A70 loss of function in the model plant Arabidopsis thaliana leads to early embryo development failure . Another interesting sequence mapped onto the ACR is a K homology (KH) domain-containing protein, which is an RNA-binding protein implicated in mRNA stability and regulation of gene expression at the post-transcriptional level ,. KH proteins have been associated with maintenance of an inactive chromatin state in knox genes located within the peripheral zone of the shoot apical meristem required for proper leaf development in maize .
Transcriptomic surveys have enabled the identification of numerous candidate genes associated with aposporous apomixis in plant species such as Brachiaria brizantha, Poa pratensis, Paspalum notatum, Panicum maximum, Boechera spp., Paspalum simplex and Hieracium spp. -. Comparative transcriptomic analysis of Paspalum notatum has suffered from several major drawbacks commonly found in apomictic systems: lack of genuine near-isogenic apomictic and sexual lines, high heterozygosity, and limited genomic resources (reviewed in ). RNA profiling assays based on differential display have been designed to overcome these difficulties and have been used to identify a set of 45 candidates usually down-regulated during apomictic development compared with sexual formation ,. Interestingly, two of these genes (N4 and N69) show significant similarity to genes encoding RNA methyltransferases .
The identification of an RNA-N6-adenosine-methyltransferase gene and an RNA-binding protein gene within the Paspalum notatum ACR, coupled with two additional RNA methyltransferases differentially expressed in flowers of sexual and apomictic plants, prompted us to explore the possible role of RNA methylation in aposporous reproductive development. As part of this effort, we sought to infer the possible function of the N69 cDNA candidate in reproductive development. To accomplish this goal, we characterized the candidate, identified its putative orthologs in model species, and analyzed its expression in reproductive tissues of sexual and apomictic genotypes at key developmental steps.
N69 sequence characterization
Primers used to recover partial and complete PnTgs1-like sequences from apomictic and sexual genotypes (fragments F1, F2, F3, F4)
Correlation of PnTgs1-like expression with reproductive behaviors
To determine whether this differential expression was genuinely associated with the reproductive mode, we investigated PnTgs1-like expression in spikelets collected at anthesis from three sexual and three apomictic F1 plants derived from a Q4188 × Q4117 cross. All genotypes showed PnTgs1-like expression levels similar to those observed in the corresponding sexual and apomictic progenitors (Figure 2B).
PnTgs1 representation in Paspalum notatum genotypes with variable levels of apospory expression
Finally, we detected similar PnTgs1-like expression levels in vegetative tissues (leaves and roots) of sexual and apomictic plants (Additional file 1). PnTgs1expression was detectable at levels that were lower but did not differ significantly from those measured in floral tissues. These results indicate that this gene might be performing a common role in non-reproductive tissues of both apomictic and sexual plants, but display a specific function in floral tissues associated with the reproductive mode.
In situ localization of PnTgs1-like expression
Using in situ mRNA hybridization, we investigated PnTgs1-like expression in Paspalum notatum spikelets sampled at two developmental stages critical to the success of apospory, late premeiosis/meiosis and anthesis, respectively concomitant with aposporous initial differentiation and embryo parthenogenesis.
These results indicate that PnTgs1-like is active in the nucellus of sexual Paspalum notatum plants from early developmental stages until maturity, whereas expression is strongly reduced throughout reproductive development in apomictic genotypes.
The N69 cDNA fragment was initially recovered during screening to identify transcriptional differences between spikelets collected from sexual and apomictic Paspalum notatum plants . Subsequent sequence analysis revealed that this fragment belongs to a gene encoding PIMT (PRIP-interacting protein with methyltransferase domain)/TGS1, a methyltransferase involved in sn(o)RNA biogenesis, mRNA splicing, and coactivation of PPAR (peroxisome proliferator activated receptor)-regulated gene expression (reviewed in ).
PIMT/TGS1, first isolated as a transcriptional co-activator PRIP-interacting protein from Saccharomyces cerevisiae , has been extensively studied in yeast, flies, and mammals (reviewed in ) but remains poorly characterized in plants. Interestingly, all eukaryotes possess a single tgs1 copy—except for plant genomes, which usually carry at least two copies. PIMT/TGS1 typically contains a methyltransferase domain and two binding domains; this structure allows interactions with RNA and S-adenosyl-L-methionine, the methyl donor in the methyl transfer reaction . The post-transcriptional conversion of 7-methylguanosine caps (m7G) into 2,2,7-trimethylguanosine (m3G) catalyzed by PIMT/TGS1 plays a central role in the biogenesis of sn(o)RNAs and telomerase RNAs ,. In addition, PIMT/TGS1 is pivotal for transcriptional modulation in several contexts. It interacts with and co-localizes to the nucleus along with histone acetyl transferase (HAT)-containing transcriptional coactivators such as CBP/Ep300 and non-HAT-containing coactivators such as the Mediator subunit Med1 (PPAR binding protein; PBP/TRAP220/DRIP205) and PRIP ,,. PIMT has been proposed to serve as a molecular bridge between HAT- and non-HAT-containing transcriptional complexes and to control nuclear receptor-mediated transcription. Moreover, ERK2 phosphorylation at Ser298 of PIMT/TGS1 activates transcriptional activity at some promoters, suggesting a direct role for signal transduction pathways in modulating transcription .
The abolishment of PIMT/TGS1 function causes a wide range of phenotypic defects in different eukaryotic non-plant model systems. In S. cerevisiae, these alterations consist of cold-sensitive splicing defects, growth delay at low temperatures, loss of nucleolar structural organization, pre-rRNA processing deficiency, and meiotic failure after aberrant splicing of key regulators ,,. In mammals, PIMT/TGS1 loss of function leads to alteration of cell cycle progression, embryo lethality, and increased hepatic gluconeogenesis -. In Drosophila, embryo lethality in the early pupal stage has been reported .
Interestingly, comparative transcriptomic analyses of sexual vs. apomictic reproduction in plants, including Paspalum notatum, have provided sets of modulated genes enriched in ontological families strongly associated with PIMT/TGS1 function in eukaryotes. A major set consists of ribosomal RNAs and ribosomal protein genes ,,, an observation consistent with the role of PIMT/TGS1 in both nucleolar organization and pre-rRNA processing . Other TGS1-related functional classes that are differentially expressed in sexual and apomictic plants are proteasome-related proteins, cytoskeletal proteins, and ERK2 cascade member genes ,,. With regards to the body of data collected in non-plant species for TGS1 function, our observations for reduced expression of PnTgs1-like during female reproductive development in apomictic genotypes suggests that the transition from sexuality to aposporous development might depend on alterations of the splicing-machinery operating in conjunction with ERK2-mediated transcriptional regulation. Such differential expression was not observed in vegetative tissues. Whether a reduction of PnTgs1-like expression is causal for apomixis and which mechanisms are responsible for the differential expression in reproductive tissues definitively require further investigations, including trimethylguanosine synthase activity assays, RNA methylation profiling, and mutant analysis in model plant species.
Comparative transcriptional analyses and mutant characterization have revealed that apomictic developments likely emerged after alterations in the prevailing transcriptional dynamics of reproductive tissues or cells of sexual plants . In particular, expression patterns in female reproductive tissues or cells are modulated during development by specific RNA-dependent DNA methylation pathways and, interestingly, some chromatin-remodeling enzymes participating in these pathways are down-regulated in maize-Tripsacum apomictic hybrids; their loss of function in maize causes profound reshaping of transcriptional activities and developmental heterochronicity partially mimicking apomictic developments ,. Defining the nature of the sequences targeted by these silencing pathways is critical to resolve two issues: the precise identification of these pathways’ roles in the evolution of apomictic reproduction from sexuality, and the elucidation of the mechanisms responsible for their chronological and spatial inhibition. With regard to the latter question, we believe that the function of TGS1 in both RNA biology and transcriptional pattern regulation offers the basis for an attractive model involving altered RNA processing to explain coordinated loss of function of key regulators.
Our results indicate that PnTgs1-like shows high expression in nucellar cells of sexual plants while its representation is significantly reduced in aposporous plants. Moreover, PnTgs1 expression levels are negatively correlated with the occurrence of AESs. At the same time, genes usually associated with PIMT function (such as rRNA and ribosomal protein genes) have been reported by our research group  and others , to be differentially expressed between sexual and apomictic plants. These findings suggest that PnTGS1-like may participate in the repression of AES formation in nucellar cells surrounding the legitimate germ cell lineage. To confirm our hypothesis of a pivotal role for methylation-dependent RNA processing in the emergence of asexual reproductive pathways, we are currently using a transformation platform recently established in our laboratory  to assess the effects of the plant specific TGS1-like protein on the reproductive development of plant model species and Paspalum notatum.
The following tetraploid (2n =4x =40) Paspalum notatum genotypes were used in this study: i) fully apomictic genotypes Q4117 and Q4012 ,; ii) facultative apomictic genotypes Q4064 and U47 ; iii) fully sexual genotypes C4-4x and Q4188 ,; and iv) three fully sexual (#43, #60, #93) and three fully apomictic (#40, #65, #74) F1 hybrids derived from a Q4188 × Q4117 cross ,. The Paspalum notatum genotypes were obtained from the IBONE live germplasm collection (Instituto de Botánica del Nordeste, IBONE-CONICET, Argentina).
RACE experiments  were conducted, following the manufacturer’s instructions, on two cDNA Marathon libraries (Clontech, Mountain View, California, USA) produced from Q4117 and Q4188 mRNA samples extracted from spikelets during late premeiosis/meiosis (developmental stages I/II of Laspina et al. ). Primers were designed with Primer 3 Plus (http://www.bioinformatics.nl/cgi-bin/primer3plus/primer3plus.cgi/) . PCR amplifications were performed using a DNA Engine Peltier thermal cycler (Bio-Rad, Hercules, California, USA) in 25-μl reactions containing tricine buffer (0.01 M tricine and 0.1 mM EDTA) supplemented with 1 μl of a 1:250 Marathon library dilution, 0.2 μM of each specific primer, 0.2 μM AP1 primer (matching the Marathon adapter AP1), 1× Taq-LOADTM Mastermix (MP Biomedicals), 1.5 U Taq polymerase (Promega, Madison, Wisconsin, USA), 1.5 mM MgCl2, and 200 pM dNTPs. Amplicons were electrophoresed on 1.5% (w/v) agarose gels and stained with 1% (v/v) ethidium bromide. Fragments of interest were purified with a QIAquick gel extraction kit (Qiagen, Valencia, California, USA), cloned into a p-GEM-T Easy vector (Promega), and transferred by thermal shock into Escherichia coli DH5α TOPO competent strands (Invitrogen/Life Technologies, Carlsbad, California, USA). Plasmids were purified using a QIAprep Spin Miniprep kit (Qiagen), and the amplified RACE fragments were sent to Beckman Coulter Genomics (London, UK) for sequencing.
For pyrosequencing, Q4117 (apomictic) and C4-4x (sexual) total RNA samples were extracted from balanced bulks of spikelets collected at premeiosis, meiosis, postmeiosis, and anthesis. mRNA enrichment, library preparation, emulsion PCR, 454 Genome Sequencer FLX + (Roche, Penzberg, Germany) sequencing, and bioinformatic analysis were performed by INDEAR (Instituto de Agrobiotecnología de Rosario, Rosario, Argentina).
The RACE fragment sequence was trimmed using the VecScreen algorithm at NCBI (www.ncbi.nlm.nih.gov), and the primer sequences were eliminated using Sequencher 4.1.4 (Gene Codes Corporation). The PnTgs1-like contig was then assembled in Sequencher from the RACE extended N69 sequence and the Roche 454 transcripts. BLASTN and BLASTX similarity analyses were conducted using NCBI (www.ncbi.nlm.nih.gov) and Gramene database (http://ensembl.gramene.org/genome_browser/index.html). Alignments were performed using Clustal Omega at the EBI-EMBL website (http://www.ebi.ac.uk/Tools/msa/clustalo/). Open reading frames were located with ORF finder (http://www.ncbi.nlm.nih.gov/gorf/), and translation was carried out using the ExPASy translate tool (http://web.expasy.org/translate/).
Quantitative real-time PCR
Total RNA was extracted from spikelets collected at several developmental stages (premeiosis, meiosis, postmeiosis, and anthesis) using an SV Total RNA isolation kit (Promega). cDNAs were synthesized from 1 μg of total RNA using Superscript II retrotranscriptase (Invitrogen/Life Technologies). Quantitative real-time PCR amplifications were performed in 25-μl final reaction volumes containing 200 nM gene-specific primers (N69F1 and N69R1; Table 1), 1× qPCR Real Mix (Biodynamics, Buenos Aires, Argentina), and 20 ng cDNA. Amplifications were performed in a Rotor-Gene Q thermocycler (Qiagen) programmed as follows: 2 min at 94°C followed by 45 cycles of 15 s at 94°C, 30 s at 55°C, and 40 s at 72°C. A melting curve (10-s cycles from 72 to 95°C, with the temperature increased by 0.2°C per cycle) was produced at the end of the cycling period. Quantitative real-time PCRs were performed in triplicate from cDNAs obtained from two biological replicates. Values were normalized using β-tubulin as an internal reference gene, since in former work this gene was reported to show a stable representation in flowers of sexual and apomictic plants of the same ploidy level in Poa pratensis and Paspalum notatum ,,. Relative expression levels were calculated using REST-RG software (Corbett Life Sciences).
In situhybridization experiments
Spikelets of sexual (Q4188) and apomictic (Q4117) Paspalum notatum genotypes were collected and fixed in a solution of 4% paraformaldehyde/0.25% glutaraldehyde/0.01 M phosphate buffer (pH 7.2), dehydrated in an ethanol/xylol series, and embedded in paraffin. Specimens were sliced into 10-μm-thin sections and placed onto slides treated with 100 μg ml−1 poly-L-lysine. Paraffin was removed with a xylol/ethanol series. Both sense (T7) and antisense (SP6) RNA probes were produced using a plasmid containing the N69 5′ RACE clone. Probes were labeled using a Roche DIG RNA labeling kit (SP6/T7) and hydrolyzed into 150–200-bp fragments. Following prehybridization at 37°C for 10 min in 0.05 M Tris–HCl buffer (pH 7.5) containing 1 μg ml−1 proteinase K, hybridization at 37°C was performed overnight in a buffer containing 10 mM Tris–HCl (pH 7.5), 300 mM NaCl, 50% deionized formamide, 1 mM EDTA (pH 8), 1× Denhardt’s solution, 10% dextran sulfate, 600 ng ml−1 total RNA, and 60 ng of the corresponding probe. Detection was performed following the Roche DIG detection kit instructions using anti-DIG AP and NBT/BCIP as substrates.
Availability of supporting data
The data set supporting the results of this study is included within the manuscript and its additional file(s).
This work was supported by the collaborative ECOS-MINCyT France-Argentina program (Project A11B02); Agencia Nacional de Promoción Científica y Tecnológica, Argentina (Project PICT 2011–1269); Universidad Nacional de Rosario, Argentina (Project AGR189) and Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina (Project PIP 11220090100613). Authors L. Siena, J. P. A. Ortiz, and S. Pessino are research staff members of CONICET.
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