Dandan Yang1
Huachao Xu
Muhammad Ali
Xiangyang Xu
Gang Lu- 1Department of Horticulture, Zhejiang University, Hangzhou, China
- 2College of Horticulture, Northeast Agricultural University, Harbin, China
- 3Key Laboratory of Horticultural Plant Growth, Development and Quality Improvement, Ministry of Agricultural, Zhejiang University, Hangzhou, China
Cold stress is a serious threat to subtropical crop pollen development and induces yield decline. N6-methyladenosine (m6A) is the most frequent mRNA modification and plays multiple physiological functions in plant development. However, whether m6A regulates pollen development is unclear, and its putative role in cold stress response remains unknown. Here, we observed that moderate low-temperature (MLT) stress induced pollen abortion in tomato. This phenotype was caused by disruption of tapetum development and pollen exine formation, accompanied by reduced m6A levels in tomato anther. Analysis of m6A-seq data revealed 1,805 transcripts displayed reduced m6A levels and 978 transcripts showed elevated m6A levels in MLT-stressed anthers compared with those in anthers under normal temperature. These differentially m6A enriched transcripts under MLT stress were mainly related to lipid metabolism, adenosine triphosphatase (ATPase) activity, and ATP-binding pathways. An ATP-binding transcript, SlABCG31, had significantly upregulated m6A modification levels, which was inversely correlated to the dramatically downregulated expression level. These changes correlated with higher abscisic acid (ABA) levels in anthers and disrupted pollen wall formation under low-temperature stress. Our findings characterized m6A as a novel layer of complexity in gene expression regulation and established a molecular link between m6A methylation and tomato anther development under low-temperature conditions.
Introduction
In flowering plants, male reproductive development is vulnerable to abiotic stress (Al Mamun et al., 2010; De Storme and Geelen, 2014; Sharma and Nayyar, 2016; Kiran et al., 2019). Frequent temperature fluctuations cause male sterility in most crops, leading to lower fruit and seed set and final yield (Pacini and Dolferus, 2019). The male gametogenesis of plants depends on a series of complicated processes that lead to the development of premeiotic pollen mother cells into mature pollen grains. The male gametogenesis stage most sensitive to temperature stress is the transition from tetrad to uninucleate microspore (Kim et al., 2001; Oliver et al., 2005; Oda et al., 2010).
Increasing evidence indicates that male sterility induced by low- or high-temperature stresses is linked to tapetal dysfunction. The tapetum is the innermost sporophytic cell layer of the anther wall; it provides nutrients and precursors for microsporogenesis and pollen wall formation through programmed cell death (PCD)-triggered degradation (Ma, 2005; Ariizumi and Toriyama, 2011). The tapetum is the most susceptible to temperature fluctuations at the young microspore stage (Müller and Rieu, 2016). For instance, heat stress induces premature tapetum degeneration in Arabidopsis thaliana (Baron et al., 2012), rice (Ku et al., 2003), and wheat (Omidi et al., 2014). Conversely, cold stress disturbs tapetum development by delaying or inhibiting tapetal PCD (Liu et al., 2019). Various signaling pathways play pivotal roles in tapetum development and degeneration processes, including hormone and sugar signaling (Wang et al., 1999; Sun et al., 2019). Oliver et al. (2007) reported that in rice, male gametogenesis occurring under low-temperature stress, increased abscisic acid (ABA) levels and suppressed the expression of the tapetum-specific cell wall invertase (CWIN), OsINV4, and monosaccharide transporter genes, OSMST8 and OSMST7. These expression changes interfere with tapetum PCD and lead to pollen abortion (Oliver et al., 2007).
As sessile organisms, plants have developed a variety of responses to tolerate environmental stress, including transcriptional, post-transcriptional, and post-translational regulatory processes (Barrero-Gil and Salinas, 2013; De Storme and Geelen, 2014; Guerra et al., 2015; Zhu, 2016). Post-transcriptional modifications based on RNA alternative splicing, processing, and modification shape the transcriptome in response to abiotic stress. While, N6-methyladenosine (m6A), a methylation at the N6 position of adenosine, is the most abundant internal mRNA modification, which plays an important role in post-transcriptional gene expression regulation (Yue et al., 2015) by affecting RNA splicing (Liu et al., 2015; Xiao et al., 2016), stability (Wang et al., 2014; Du et al., 2016), translation (Zhou et al., 2015), and export (Roundtree et al., 2017). m6A methylation is recognized by RNA-binding proteins (readers), and its levels are dynamically modified by RNA methyltransferases (Writers) and demethylases (Erasers) (Yue et al., 2019). Recent evidences demonstrated that m6A also participates in plant responses to various abiotic stresses. In Arabidopsis, changed m6A deposition affects RNA secondary structure under salt stress, resulting in increased stability of mRNA transcripts of abiotic stress response genes (Kramer et al., 2020). Additionally, ALKBH6 (eraser) mutation results in increased salt, drought, and heat stress sensitivity during seed germination (Huong et al., 2020).
In Arabidopsis, m6A levels vary across tissues, with a high m6A/A ratio occurring in flowers (Zhong et al., 2008). MTA (one of the earliest discovered methyltransferases in Arabidopsis) disruption results in embryo development arrest at the globular stage (Zhong et al., 2008). Furthermore, the ALKBH10B demethylase (eraser) affects floral transition by regulating mRNA m6A of key flowering genes (Duan et al., 2017). In rice, OsFIP (writer) regulates early microspore degeneration during male gametogenesis (Zhang et al., 2019). The tomato ALKBH2 participates in fruit ripening by affecting the stability of a DNA demethylase gene, SlDML2, via m6A modification (Zhou et al., 2019). These findings suggest that m6A plays essential roles in regulating reproductive developmental processes. However, whether and how m6A participates in temperature stress response during the plant male reproductive stage remain elusive.
Tomato is one of the most widely cultivated subtropical vegetable crops in the world and its fruits and seeds are mainly derived from sexual reproduction. Because of its tropical origin, tomato is extremely sensitive to low temperature. In this study, we used m6A sequencing to analyze changes in m6A methylation in response to moderate low-temperature (MLT) stress during tomato anther development. We found that m6A methylation was prevalent in tomato anther mRNA but that the levels declined upon MLT stress. Furthermore, MLT stress directly affected m6A methylation abundance on a set of transcripts that regulate corresponding gene expression involved in anther development. Finally, we demonstrated that the decreased expression of an ATP-binding transcript, SlABCG31, was inversely correlated with its high m6A deposition, which resulted in high ABA in MLT-stressed anthers. The decrease in SlABCG31 expression may also participate in aberrant pollen coat formation after low temperature exposure. Overall, we demonstrated that mRNA m6A modification was associated with anther development under low-temperature conditions.
Materials and Methods
Plant Material and Growth Conditions
The tomato (Solanum lycopersicum) cultivar “Micro-Tom” provided by the Tomato Genetics Resource Center (University of California, Davis), was used in all experiments. Plants were grown in controlled chambers with 25°C ± 1/20 ± 1°C (normal temperature, NT), 16/8-h light/dark cycles, 300 μmol photons m–2 s–1 light intensity, and 60%–70% relative humidity. Six-week-old flowering plants were exposed to a 10°C/10°C (day/night) MLT treatment for 6 days and then moved back to NT for recovery.
Pollen Phenotypic Analysis and Light Microscopy
The development stages of the tomato anther are closely correlated to the flower bud size (Brukhin et al., 2003), which were roughly classified into six different stages (I–VI) according to semithin section observation as previously described (Peng et al., 2013; Chen et al., 2018). The anther at tetrad stage (stage II) were randomly marked with color strings before exposure to low temperature, because the tetrad stage is the most sensitive to ambient temperatures (Paupière et al., 2017; Begcy et al., 2019). The samples (anther at stages I–VI) harvested immediately after 6 days of MLT treatment were named MLT. Then the MLT-stressed plants were moved back to NT for recovery growth. The samples (anthers stages III–VI) developed from the marked tetrad anther at different time intervals that corresponded to time taken by tetrad anther to reach next different anther stages (stages III–VI) were named MLTR.
Mature pollen grain viability was determined using Alexander staining (Alexander, 1969). Scanning electron microscopy (SEM) was performed as previously described (Chen et al., 2018). Semithin section analysis was performed according to a previous report (Chen et al., 2018) with minor modifications. Briefly, the samples were fixed for 12 h at 4°C with 0.1 M phosphate-buffered saline (PBS) (pH 7.2) containing 2.5% glutaraldehyde (v/v). Subsequently, they were washed thrice with 0.1 M PBS, followed by soaking in 1% osmic acid (v/v) for 1–2 h. Specimens were rewashed thrice with 0.1 M PBS and then dehydrated through a gradient ethanol series. Further, we embedded and polymerized the specimens in Spurr’s resin, and cut them into 2-μm-thick sections, which were stained with 1% methylene blue. Sections were observed and photographed under a Nikon Eclipse 90i microscope (Nikon, Japan). Terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assays were performed with the TUNEL Apoptosis Detection Kit (Roche, Switzerland) according to the manufacturer’s protocol and using 10-μm paraffin sections of anthers at different stages. Furthermore, fluorescence signals were analyzed using Nikon’s confocal laser scanning microscope, A1-SHS (Nikon, Japan).
RNA Isolation and qRT-PCR Analyses
Immediately after 6 days of MLT stress, anthers (about 0.5 g, >15 plants for each sample) at the six different stages (I–VI) were manually sampled and subjected to total RNA isolation using the Total RNA Kit II (OMEGA, United States). First-strand cDNA was synthesized using the PrimeScriptTM RT reagent kit (Takara, Japan). Quantitative RT-PCR reactions were performed using SYBR® Green Realtime PCR Master Mix (Toyobo, Japan). Reactions were run on Bio-Rad CFX96 (Bio-Rad, United States) in triplicate technical replicates and with SlUbi3 as the endogenous control. Ct values were recorded and normalized with the 2–ΔΔCt method (Livak and Schmittgen, 2001). The experiment was repeated as three independent biological replicates. Primers used for qRT-PCR analysis are listed in Supplementary Table 1.
Quantitative Analysis of m6A in Total RNA
The total RNA m6A levels were determined with the EpiQuikTM m6A RNA Methylation Quantification Kit (Colorimetric) (Epigentek, United States) following the manufacturer’s instructions. Briefly, RNA was bound to strip wells using RNA high binding solution. RNA m6A modification was captured and detected with capture and detection antibodies. Signals were enhanced and quantified colorimetrically by determining the absorbance at 450 nm using a microplate spectrophotometer with three technical replicates. Both negative and positive control RNA samples (m6A 2 μg/mL) were provided with the kit. The standard curve was generated using the positive control sample. All experiments were performed three independent times.
High-Throughput m6A Sequencing
m6A-seq was performed as previously described (Dominissini et al., 2013). The anthers (about 0.5 g) at the tetrad stage from NT- and MLT-treated plants (n > 15 plants for each sample) were collected to extract the total RNAs. Three biological replicates of m6A RIP sequencing were performed. RNA quality was checked with the Agilent 2100 bioanalyzer (Agilent, United States) and using gel electrophoresis. Separation of mRNAs from total RNAs and sequencing of immunoprecipitated mRNA and pre-immunoprecipitated mRNA (input control) was performed at Novogene Biotech (Beijing, China) using an Illumina HiSeq 4000 system. Sequence data were deposited into the NCBI Sequence Read Archive under accession BioProject ID: PRJAN713408. A total of 23–29 million clean reads were produced from each library, and more than 95% of the reads were uniquely mapped to the tomato reference genome (Tomato Genome Consortium, 2012). The MACS software was used to identify m6A peaks in immunoprecipitated samples using the corresponding input sample as the control. The strict cutoff criterion with assigned false discovery rate < 0.05 was applied to obtain high-confidence peaks (Zhang et al., 2008). Only peaks captured in all three biological samples were considered as confident peaks and used for further analysis. The de novo motif identification of the m6A peak data was carried out using the HOMER (hypergeometric optimization of motif enrichment) software (version 4.71) to obtain their position and accurate motif regions. Visualization analysis of m6A peaks was performed using the Integrated Genome Browser (Helt et al., 2009). All m6A modification sites were assigned to different transcription regions covering transcription start site (TSS), 5′ untranslated region (UTR), coding sequence (CDS), 3′UTR, and intron. The gene expression level was calculated using RPKM method (Reads Per Kilobase per Million mapped reads). Differential m6A peaks between NT and MLT anthers were determined using the m6A site differential algorithm (Meng et al., 2013) with a P-value < 0.05. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of were performed to identify the biological processes involving the differentially modified genes.
Quantification of Endogenous ABA Levels
Measurement of endogenous ABA was performed as previously reported (Chen et al., 2018) with minor modifications. Fresh anthers (about 0.5 g) at the tetrad stage were collected from NT and MLT plants (>15 plants for each sample) and ground into a powder in liquid nitrogen with a mortar and pestle. For each sample, 100 mg of powder was homogenized using 1 mL ethyl acetate spiked with d6-ABA (OlchemIm, Czechia). Samples were then agitated for 10 min and centrifuged at 13,000 g for 20 min at 4°C. The supernatant was collected and dried in N2 gas. Dried samples were resuspended in 0.2 mL of 60% (v/v) methanol and then centrifuged at 13,000 g for 10 min at 4°C. The supernatant sample was filtered through a 0.22-μm nylon membrane and analyzed using HPLC/MS-MS on an Agilent 1290 Infinity HPLC system coupled with an Agilent 6460 Triple Quad LC/MS device (Agilent, United States). Agilent Zorbax XDB C18 columns (150 mm × 2.1 mm, 3.5 μm) were used to perform the HPLC analysis. Three independent biological replicates were performed for each sample.
Statistical Analysis
All experiments were conducted in randomized complete block design. Mean values were used to represent the data of at least three independent experiments. The statistical differences between treatments were verified using two-tailed Student’s t-tests.
Results
Impact of MLT Stress on Tomato Pollen Development
To investigate tomato pollen development response to low-temperature stress, flowering tomato plants were treated with MLT (10°C/10°C) for 6 days and then moved to normal growing conditions for recovery. Plants continuously grown under NT (25°C/20°C) were used as controls (Supplementary Figure 1A). Surprisingly, after 6 days of MLT treatment, pollen viability was similar in control and stressed plants, reaching 95.0% (Figures 1A,B). Tomato reproductive organ development nearly ceases when the ambient temperature is below 12°C (Criddle et al., 1997). Therefore, the anther development may be delayed and cease under MLT-stress. We determined the viability of mature pollen grains developed from marked anthers at the tetrad stage after MLTR. Strikingly, pollen viability decreased by 95.8% after MLTR (Figures 1A,B). We also examined pollen morphology using SEM. Under NT, pollen had an elliptical shape and grain surface was densely microperforated and granulated with three germination ditches (Figure 1C). Conversely, 97.9% of MLTR-stressed pollen grains were highly shriveled and aggregated. The pollen grain surface was smooth, lacking granulation and germination ditch (Figures 1C,D). To monitor the dynamic response to MLT stress, we generated transverse semithin sections of anthers at different developmental stages and assessed their morphology. Under NT, tapetal cells formed a regular layer surrounding the locules at tetrad stage, which subsequently underwent PCD, gradually degenerating until disappearing completely at binucleate stage (Figure 1E). Anther morphology did not differ between MLT and NT plants, except for few pollen grain abortions at mature pollen stage (Figure 1E). However, under MLTR-stress, at early uninucleate stage, anther chambers were irregular and harbored numerous shriveled microspores, and tapetal cells became vacuolated. More importantly, tapetal cell degeneration was incomplete even at the binucleate stage, contributing to pollen grain abortion at the mature stage (Figure 1E). To further investigate the timing of tapetal cell degeneration in pollen development, we performed TUNEL assays on different stage anthers from plants grown under NT or MLTR conditions. Under NT, TUNEL signals were first detected on tapetal cells at the tetrad stage. They gradually intensified from the early to late uninucleate stage and finally disappeared at the binucleate stage (Supplementary Figure 1B). However, under MLTR, TUNEL signals appeared at the uninucleate stage and became weaker at the binucleate stage, suggesting that tapetal cells PCD was delayed (Supplementary Figure 1B). Our data show that pollen development was sensitive to low temperature and that plants exposed to MLT stress had pollen sterility, characterized by changes in tapetum development and exine deposition.
Figure 1. Moderate low temperature (MTL) stress at the tetrad stage affects pollen development in tomato. (A) Alexander staining of mature pollen grains from the plants exposed to normal temperature (NT), MLT-stress and returned to normal growing temperature for recovery after moderate low temperature treatment (MLTR). Scale bars = 100 μm. (C) Scanning electron microscopy indicated that MLTR-stress pollen grains were seriously shrunk and collapsed, appearing aggregated. Scale bars c1 = 10 μm; c2 = 3 μm; c3 = 1 μm. (B,D) Quantification of viable mature pollen grains and morphology normal pollen from NT, MLT, and MLTR plants, respectively. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test). (E) Semithin cross sections of anthers in different stages under NT and MLT condition. The tapetum degeneration was postponed under MLTR compare to NT condition. MMC, microspore mother cell; Tds, tetrads; UMsp, uninucleate microspore; BP, binucleate pollen; PG, pollen grains; DUMsp, degenerated uninucleate microspore; DBP, degenerated binucleate pollen; DPG, degenerated pollen grains; T, tapetum. The experiment was repeated three times independently with consistent results. Scale bars = 20 μm.
MLT Stress Influences m6A Levels and m6A-Related Gene Expression in Tomato Anthers
To determine whether m6A participates in tomato anther development and responds to suboptimal temperature stress, we performed colorimetric m6A quantification assays in plants grown under NT and MLT. Under NT conditions, overall RNA m6A levels were slightly lower at the tetrad stage than at the pollen mature cells (PMC) stage. m6A increased mildly at the uninucleate stage and peaked at the binucleate stage (Supplementary Figure 2A). However, under MLT stress, anther m6A levels were decreased at both the tetrad and uninucleate stages compared to that at NT (Figure 2A).
Figure 2. The expression profiles of m6A writers, erasers and readers under NT and MLT conditions. (A) The relative levels of m6A in total RNA of anther at stage-II and III under NT and MLT conditions. The level of m6A in stage-II under NT condition is set to 1. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test). (B) Expression patterns of genes in various tissues of plants under NT condition, especially in anther of different stages. Green, weak expression; Red, strong expression. R, root; S, stem; L, leaf; GF, green fruit; RF, red fruit; I, anther at microspore mother cell stage; II, anther at tetrad stage; III, anther at early uninucleate stage; IV, anther at late uninucleate stage; V, anther at binucleate stage; VI, anther at mature pollen stage. (C) qRT-PCR analysis of writer, erasers and readers genes in anther at different stages under NT and MLT conditions. The levels of genes expression normalized to Ubiquitin expression are shown relative to SlMTA, SlALKBH1B, and SlECT1 under NT condition set to 1, respectively. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test).
Next, we analyzed the spatial and temporal expression profiles of m6A-related components (writers, erasers, and readers) in NT tomato plants using qRT-PCR. Among the 26 investigated genes (seven writers, ten erasers, and nine readers), 23 had altered expression among different tissues or anthers at different developmental stages. The exceptions were SlMTB, SlALKBH9B, and SlALKBH10B, which had low expression levels in all 11 tested organs/tissues. The writer genes, including SlMTA, SlMTD, and SlHAKAI, were mostly expressed in tomato anthers at the mature pollen stage (VI) and fruits (Figure 2B). Several erasers, including SlALKBH2B and SlALKBH6B, were preferentially expressed in mature anthers and young fruits, whereas SlALKBH7B and SlALKBH8B were rarely expressed in reproductive tissues (Figure 2B). Moreover, SlECT1 and SlECT2 reader genes were also preferentially expressed in mature anthers and young fruits; they had higher expression levels than other readers, including SlECT3, SlECT4, and SlECT7, which had low expression in anthers at all stages except stage VI (Figure 2B). The expression profiles of m6A-related genes analyzed using qRT-PCR assay were consistent with the in silico data available from the tomato eFP Browser (Supplementary Figures 2B–D).
Since total RNA m6A levels were lower in MLT anthers at stages II and III, we further analyzed the changes in m6A-related gene expression profiles in MLT and NT anthers using qRT-PCR. SlMTA, SlMTC, and SlMTD expression significantly decreased at the microspore mother cell stage (I) under MLT stress compared with that at NT. At tetrad (II) and uninucleate (III and IV) stages, only SlMTD expression significantly decreased (Figure 2C), whereas SlMTC and SlMTD were significantly downregulated at the binucleate stage (V) under MLT stress. More importantly, all writer genes analyzed (SlMTA, SlMTC, SlMTD, SlFIP37, and SlHAKAI) were downregulated in MLT anthers at the mature pollen stage (VI) (Figure 2C). Furthermore, the SlALKBH1B eraser gene was significantly downregulated in anthers at the stages IV and VI. SlALKBH2B was significantly downregulated at stages II, III, and VI, and SlALKBH4B and SlALKBH6B were decreased at both stages V and VI (Figure 2C). However, the m6A reader SlECT1 was significantly upregulated in MLT at stage II (Figure 2C). These data indicate that m6A modification levels and the expression pattern of its related genes were changed under low-temperature stress. We speculated that m6A methylation plays a fundamental role in anther development and temperature stress responses.
Transcriptome-Wide Detection of m6A Methylation in Tomato Anthers
To explore the molecular mechanisms behind m6A regulation of anther development in tomato, we performed a transcriptome-wide detection of m6A methylation through m6A-seq using NT- and MLT- anthers at the tetrad stage. Six MeRIP libraries were analyzed (Supplementary Figure 3A) and high Pearson correlation coefficients were found between biological replicates, indicating a high reproducibility for the m6A-seq data (Supplementary Figure 3B). m6A modification sites, named m6A peaks, were identified on the basis of the comparison of read distribution between the input and immunoprecipitation samples using exomePeak with an estimated P-value < 0.05. We used high-confidence m6A peaks that were observed in all three biological replicates for subsequent analysis. A total of 10,235 and 9,911 high-confidence m6A peaks, representing 8,541 and 8,743 gene transcripts, were detected in NT and MLT anthers, respectively (Figure 3A and Supplementary Figure 3C). Among transcripts harboring m6A modification, 88.36, 9.85, 1.53, and 0.26% contained one, two, three, and more than three peaks, respectively (Figure 3B). Enrichment analysis using the KEGG revealed that these m6A-containing transcripts in NT condition were enriched in multiple conserved metabolic pathways, including tricarboxylic acid (TCA) cycle, spliceosome, proteasome, and pyruvate metabolism (Figure 3C).
Figure 3. Transcriptome-wide m6A methylation profiles in tomato anther at stage-II. (A) The number of overlapped m6A peaks identified in three biological replicates under NT and MLT conditions, respectively. The peaks identified in all three biological replicates were used for subsequent analysis. (B) Statistics on proportion of the m6A-modifited transcripts containing different m6A sites numbers in NT and MLT conditions. (C) KEGG enrichment analysis of all the transcripts with m6A peaks in NT condition.
The analyses of m6A peak distribution across the tomato transcriptome in NT anthers showed that highly enriched m6A modifications surrounded stop codon and 3′-UTRs (Figure 4A), as seen in tomato fruits (Zhou et al., 2019). Furthermore, we assigned each m6A peak to one of five transcript segments based on their location: TSS, 5′-UTR, CDS, stop codon (a 100-nucleotide window centered on the stop codon), and 3′-UTR. These analyses revealed that m6A peaks were abundant near stop codons (49.04%) and 3′-UTRs (40.34%), followed by CDS (9.12%) (Figure 4B). After segment normalization by the total length of each gene portion, we confirmed that m6A peaks were predominantly enriched around the stop codon and 3′-UTR (Figure 4B). Homer was used to identify the sequence motifs enriched within the m6A peaks in tomato anthers and it showed that UGUAYY (where Y represents A, G, U, or C) was the most statistically over-represented motif (Figure 4C). This phenomenon was observed previously in Arabidopsis and tomato fruits (Luo et al., 2014; Zhou et al., 2019), suggesting that m6A methylation sequence motifs are conserved between Arabidopsis and tomato.
Figure 4. Distribution pattern of m6A peaks along the transcripts and the sequence motif in tomato anther. (A) m6A peaks summits localization along the transcripts in NT and MLT conditions. Each transcript is divided into three parts: 5′-UTR, CDS and 3′ -UTR. UTR, untranslated region; CDS, coding sequence. (B) The m6A peaks summits and relative enrichment in five non-overlapping transcripts segments in NT and MLT conditions. TSS, transcription start site. (C) The conserved sequence motif for m6A peaks in NT and MLT conditions.
Comparison Between NT and MLT Anther m6A Methylation Profiles
To systemically elucidate the m6A methylome response to low temperature, we compared NT and MLT m6A-seq data. There was no obvious difference in whole transcriptome m6A distribution between NT and MLT anthers (Figure 4A). The analysis showed that 7,846 m6A modified transcripts containing 9,396 m6A peaks were shared by MLT and NT (Figure 5A and Supplementary Figure 3D). However, a total of 3,837 m6A peaks harboring 3,434 gene transcripts differed between NT and MLT anthers in m6A levels (P-value < 0.05) (Supplementary Table 2). Among them, the m6A peaks of 2,783 transcripts appeared in stop codons or 3′-UTRs; the m6A levels of 978 of these transcripts were higher in MLT than in NT, whereas the inverse was true for 1,805 transcripts (Figure 5B and Supplementary Table 2). These data suggested that MLT stress markedly affected m6A levels in a large number of mRNA transcripts, which are predominantly downregulated.
Figure 5. Comparative analysis transcriptome-wide m6A profiles between NT and MLT anthers at stage-II. (A) The number of overlapped m6A peaks between NT and MLT anthers. (B) The gene number of transcripts with differential m6A enrichment and differential transcript levels between NT and MLT anthers. (C) GO analysis significantly different enrichment peaks related genes between NT and MLT anthers.
To identify the potential correlation between m6A levels and transcript abundance in tomato anthers, we investigated the transcript levels of genes under MLT stress and NT by RNA-seq. Among the 1,805 transcripts with lower m6A levels in MLT anthers, 70.2% were upregulated under MLT stress, whereas 29.8% were downregulated. Accordingly, among 978 transcripts with higher m6A levels in MLT anthers, 569 had lower expression levels in MLT-stressed anthers (Figure 5B). These results revealed that m6A methylome in stop codon or 3′-UTR generally negatively correlated with the transcript levels. KEGG analysis showed that, under MLT stress, transcripts with increased m6A methylation were significantly enriched in phenylalanine, tyrosine, and tryptophan metabolism and amino acid biosynthesis pathways. Furthermore, transcripts with decreased m6A were significantly enriched in mRNAs for surveillance and carbon metabolism pathways (Supplementary Figure 4). These metabolic pathways may be associated with plant pollen development (Yang et al., 2001; Min et al., 2014; Fang et al., 2016).
MLT Stress Induces the m6A Level Alteration in Anther-Related Transcripts
To further analyze m6A response to MLT stress during anther development, we performed GO analysis of the transcripts that were significantly differentially modified by m6A methylation (| log2FoldChange| > 1 and P-value < 0.05) between NT and MLT stress. In MLT anthers, transcripts with decreased m6A methylation were significantly enriched in “cellular lipid metabolic process,” “regulation of RNA biosynthetic process,” and “adenosine triphosphatase (ATPase) activity-related function” categories (Figure 5C). Whereas the transcripts with increased m6A methylation under MLT stress were significantly enriched in “carbohydrate derivative binding,” “nucleoside phosphate binding,” “anion binding,” and “ATP-binding” categories (Figure 5C). These changed pathways play important roles in anther development (Lucca and León, 2012; Shi et al., 2015; Zhao et al., 2016).
We further analyzed the expression patterns of the significantly differentially modified transcripts in response to MLT stress. The transcripts of diacylglycerol acyltransferase 1 (SlDGAT1) and inositol-3-phosphate synthase 2 (SlMIPS2), which are involved in lipid metabolism, were significantly upregulated under MLT stress and had decreased m6A levels (Figure 6). Conversely, calcium-transporting ATPase isoform 2 (SlACA2) expression was downregulated under MLT stress (Figure 6C). The transcript levels of factors with decreased m6A modification, including WRKY DNA-binding protein 33 (SlWRKY33), auxin response factor 9B (SlARF9B), and ethylene response factor 3 (SlESE3), were significantly upregulated in MLT anthers (Figure 6). Additionally, the expression of the ATP-binding member of ATP-binding cassette G31 (SlABCG31), CTR1-like protein kinase (SlCTR1), and receptor-like kinase 1 (SlRLK1) genes, which had high m6A methylation levels, was downregulated under MLT stress (Figure 6C). Overall, these data implied that MLT stress affected m6A methylation of various transcripts, altering their expression levels to regulate pollen development.
Figure 6. Comparison on m6A levels and expression levels of transcripts in NT and MLT anthers at stage-II. (A) Integrative Genome Browser (IGB) showing m6A-seq read distributions in transcripts. The red arrowheads indicate the position of m6A peaks with significantly changed m6A enrichment in MLT-stress stage-II anther compared to NT. The white arrowheads represent the direction of gene. (B) The m6A enrichment of transcripts involved in pollen development in NT and MLT anthers. The level of m6A in stage-II under NT condition is set to 1. Each value is the mean ± SD (n = 3 biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test). (C) qRT-PCR analysis validates the different m6A enrichment peak related genes expression levels between NT and MLT anthers. The levels of genes expression normalized to Ubiquitin expression are shown relative to genes expression under NT condition set to 1, Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test).
MLT Stress Increases SlABCG31 m6A Levels and ABA Content
Because m6A levels changed in transcripts that may be involved in pollen development under MLT stress, such as SlDGAT1, SlMIPS2, SlACA2, and SlABCG31 (Figures 5C, 6), we further examined the underlying mechanisms of pollen development regulation by m6A methylation. Members of the ATP-binding cassette transporter (ABC) family, particularly ABC sub-family G members, are involved in ABA transport. Accordingly, AtABCG31 functions in exporting ABA from the endosperm to the embryo in Arabidopsis (Borghi et al., 2015; Kang et al., 2015). The tomato SlABCG31 is highly homologous (71%) to AtABCG31 (Supplementary Figure 5). To identify whether SlABCG31 participates in pollen development under MLT stress, we analyzed its expression with qRT-PCR in different tomato tissues and anthers at different developmental stages. The data revealed that SlABCG31 is predominantly accumulated in anthers and is rarely detected in other tissues and organs (Figure 7A). Because SlABCG31 expression sharply decreased under MLT stress (Figure 6B), we investigated whether it affected ABA levels in MLT anthers. Surprisingly, endogenous ABA levels measured using HPLC–mass spectrometry were noticeably increased in MLT anthers than in NT anthers at the tetrad stage (Figure 7B). Furthermore, qRT-PCR data revealed that the expression of the ABA signaling-related genes, SlPYLs and SlPP2Cs, was significantly changed under MLT stress (Supplementary Figure 6). SlPYL4, which had the highest expression level at the tetrad stage, was significantly decreased in MLT anthers. SlPP2C1 and SlPP2C3 were significantly upregulated under MLT stress compared with those under NT condition.
Figure 7. The expression profiles of SlABCG31 and ABA levels in anther under NT and MLT conditions. (A) qPCR analysis of SlABCG31 in various tissues of tomato, especially in anther at different stages. The genes expression levels normalized to Ubiquitin expression are shown relative to root set to 1. R, root; S, stem; L, leaf; GF, green fruit; RF, red fruit; I, anther at microspore mother cell stage; II, anther at tetrad stage; III, anther at early uninucleate stage; IV, anther at late uninucleate stage; V, anther at binucleate stage; VI, anther at mature pollen stage. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). (B) ABA levels in anther at stage-II under MLT-stress were increased in comparison to NT condition. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test). (C) The expression levels of SlCWINs genes in anther at stage-II and III in NT and MLT conditions. The levels of genes expression normalized to Ubiquitin expression are shown relative to the expression of SlCWIN7 in NT condition set to 1. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). *P < 0.05; **P < 0.01 (two-tailed Student’s t- test).
Increased ABA levels lead to high pollen abortion through negative regulation of CWIN expression, which may distort the anther carbohydrate pool (Oliver et al., 2007). Our qRT-PCR analysis showed that SlCWIN7 and SlCWIN9 were strikingly downregulated at the uninucleate stage under MLT stress (Figure 7C). Overall, we speculate that MLT stress increased m6A methylation in SlABCG31, resulting in its decreased expression, which in turn increased the ABA content in tomato anthers to suppress SlCWINs expression and cause pollen abortion (Figure 8).
Figure 8. A working model for m6A methylation affects pollen development under MLT-stress. MLT, moderate low temperature; TFs, transcript factors; Blue letters means transcripts with lower m6A levels, and red letters means transcripts with higher m6A levels; Red and green boxes represent unregulated and downregulated genes expression levels, respectively; Red arrow, significant increase.
Discussion
N6-methyladenosine methylation is the most prevalent type of internal mRNA modification in eukaryotes. Previous studies revealed that m6A modification plays essential roles in embryo development, shoot stem cell fate, root development, and floral transition in Arabidopsis (Vespa et al., 2004; Zhong et al., 2008; Bodi et al., 2012; Růžička et al., 2017). In tomato, m6A methylation participates in fruit ripening regulation through SlALKBH2, which mediates the m6A methylation of SlDML2 transcripts (Zhou et al., 2019). Recent study revealed that the OsFIP methylase may regulate early microspore development in rice (Zhang et al., 2019). Although the roles of m6A in plant growth and development have been demonstrated, mostly in Arabidopsis, its involvement and putative functions in the response to abiotic stress are still unknown. Here RNA methylome analysis revealed that mRNA m6A methylation is widespread in tomato anthers and is disturbed in response to low-temperature stress. Changes in m6A methylation may affect the expression of the genes involved in tapetum and microspore development through multiple pathways, at least partly through modifying ABA signaling genes (Figure 8).
Under normal growing conditions, anthers at the tetrad stage take about 6–7 days to reach the mature pollen stage. However, the reproductive development may slow down after exposure to low temperature stress. In our study, after 6 days MLT-stress, the marked anthers were still at tetrad stage, suggesting that at 10°C cold stress, the tomato anthers development nearly ceases, which is consistent with previous study showing that tomato reproductive organ development ceases when the ambient temperature is below 12°C (Criddle et al., 1997). Therefore, it is not surprising that the viability of mature pollen grains harvested immediately after 6 days (MLT) was similar to that in NT conditions. However, when the plants were moved back to NT conditions for recovery after cold stress, the marked anthers need another 6–7 days to reach the mature pollen stage (MLTR), and the mature pollen grains exhibited highly aborted (Figure 1E). Our cytological observations showed that low-temperature-induced pollen abortion could be attributed to delayed tapetal cell degradation at tetrad and early uninucleate stages, resulting in impaired pollen wall formation and pollen abortion (Figure 1). Correspondingly, m6A levels in total RNA were significantly decreased in anthers at both tetrad and uninucleate stages after MLT exposure (Figure 2A). Furthermore, SlMTD expression was significantly decreased at tetrad and early uninucleate stages, whereas SlECT2 was dramatically overexpressed at the tetrad stage under MLT stress (Figure 2C). m6A-seq analysis revealed that MLT treatments significantly altered the m6A levels of 2,783 transcripts in tomato anthers at the tetrad stage, which may contribute to abnormal pollen development. These data indicated that m6A modification might be involved in tomato anther development under MLT stress. Among the altered transcription, 65% were downregulated. Similarly, in rice, knockouts of the methylase genes, OsFIP or OsMTA2, dramatically reduced m6A levels and resulted in microspore degeneration at the uninucleate stage and in a male sterility phenotype (Zhang et al., 2019). These results support the speculation that m6A methylation participates in male developmental regulation. However, our findings firstly reveal that m6A methylation may be involved in low-temperature stress responses during anther development.
Growing evidence suggests that diverse abiotic stresses can change transcript m6A methylation levels (Hu et al., 2019; Huong et al., 2020; Liu et al., 2020). Moreover, m6A levels usually negatively regulate gene expression by influencing mRNA stability and the subsequent protein synthesis process (Shen et al., 2016; Duan et al., 2017; Zhao et al., 2017). By combining MeRIP-seq and RNA-seq analyses on NT and MLT anthers at the tetrad stage, we revealed that, at the transcriptome-wide level, transcript m6A enrichment was usually inversely correlated with gene expression levels under MLT stress (Figure 5B). Some of these transcripts are involved in lipid metabolism, ATPase activity, and ATP-binding processes and these pathways have been well characterized in plant male organ reproduction (Figures 5C, 6; Lucca and León, 2012; Shi et al., 2015; Zhao et al., 2016). These results suggest that changes in m6A methylation under MLT stress may affect target mRNA abundance, ultimately leading to pollen abortion. Several studies revealed abiotic stress causes transcriptome-wide redistribution of the m6A modification. For example, heat shock increases m6A enrichment at 5′-UTRs, and it mainly mapped to regions surrounding stop codons in NT condition. The m6A modification at 5′-UTR promotes mRNA cap-independent translation initiation (Meyer et al., 2015). It is noteworthy that in this study, the distribution of m6A peaks in transcripts from tomato anthers were all enriched in stop codons and 3′-UTRs under NT and MLT conditions (Figure 4), suggesting that low temperature stress affects m6A levels of transcripts but not the m6A distribution regions on the transcripts.
ABA plays vital roles in developmental processes and mediates plant response to abiotic stress. Evidence supports that ABA signaling pathways involved in abiotic stress response differ between reproductive organs and vegetative tissues (Sharma and Nayyar, 2016). During vegetative development, increased ABA levels improve abiotic stress tolerance; exogenous ABA application enhances cold tolerance in citrus leaves, and up-regulation of ABA biosynthesis genes enhances drought resistance in petunia seedlings (Melgoza et al., 2014; Estrada-Melo et al., 2015). Previous studies revealed a negative relationship between ABA content in anthers and pollen fertility under cold stress (Sharma and Nayyar, 2016). Consistently, in our study, ABA levels were significantly increased in MLT anthers at the tetrad stage (Figure 7B). SlPYLs and SlPP2Cs gene families encode ABA signal transduction core components during tomato development and abiotic stress. ABA perception by the PYLs proteins suppressed PP2C-meidated dephosphorylation of the SnRKs and allows their activate ABA responsive genes (Raghavendra et al., 2017). Here, expression levels of ABA signal transduction core genes, SlPYL4 was significantly downregulated and SlPP2C1 and SlPP2C3 were significantly upregulated by MLT stress (Supplementary Figure 6), suggesting that the ABA signal pathway regulates anther development under MLT stress. Numerous studies revealed that ABA accumulation in rice anthers under cold stress suppresses the expression of the tapetum-specific gene OsINV4 and of sugar transport genes. It disturbs tapetum PCD, resulting in pollen abortion (Oliver et al., 2005; Ji et al., 2011). Previous studies have also reported that tomato anther carbohydrate levels were alerted responding to temperature stress (Pressman et al., 2002; Firon et al., 2006). Surprisingly, nearly all SlCWINs genes in our study were significantly downregulated under MLT stress. SlCWIN7, the rice homolog to OsINV4, was dramatically downregulated at both tetrad and early uninucleate stages (Figure 7C), which might distort anther sugar metabolism and, consequently, lead to pollen sterility in tomato (Figure 1).
Baron et al. (2012) reported that enhancing ABA biosynthetic gene expression or decreasing ABA transport gene expression leads to increased ABA content in Arabidopsis inflorescence meristems under cold stress (Baron et al., 2012). Moreover, the tomato gene, SlABCG31, may participate in ABA transport and is predominantly expressed in anthers (Figure 7A); however, it was significantly downregulated at the tetrad stage under MLT stress. In addition, we found an enhancement in its m6A methylation under MLT stress, suggesting that the decrease in SlABCG31 transcript levels might result from its high m6A methylation (Figure 6). Down-regulation of SlABCG31 results in high ABA content in tomato anthers and disturbs sugar metabolism, which may be associated with pollen abortion (Figure 8). Furthermore. in Arabidopsis AtABCG31 also participates in the accumulation of sterol for pollen coat formation, and the Atatabcg31 mutant displays collapsed or sticking pollen grains (Choi et al., 2014). Interestingly, in our study, tomato MLT-treated pollen grains also displayed severe collapse and aggregation phenotypes, with differences in pollen coat sculptured surfaces compared to that in NT conditions, which resembles the Atatabcg31 mutant (Figure 1B).
In conclusion, this study reveals a unique property of anther growth under MLT stress. MLT-induced pollen abortion is the consequence of disrupted microgametogenesis, tapetum degeneration, and pollen wall formation, which may be related to differential m6A modification of transcripts (Figure 8). m6A modification is associated with ABA transport in anthers or sterol accumulation for pollen wall formation by targeting the ATP-binding cassette G gene, SlABCG31. Considering that pollen development and m6A methylation are complex processes, the molecular mechanisms behind m6A methylation function in pollen development under temperature stress should be further studied.
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Author Contributions
GL and DY conceived the study. DY, HX, YL, and ML carried out the experiment. DY, XX, and MA performed the data analysis. DY and GL wrote the article. All authors discussed and commented on the final manuscript.
Funding
This work was supported by grants from the National Key Research and Development Program of China (2018YFD1000800), the National Natural Science Foundation of China (31772316 and 31471878), and the Natural Science Foundation of Zhejiang Province, China (LZ17C150002).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Jingquan Yu (Zhejiang University, China) for support during hormone analysis.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2021.687826/full#supplementary-material
Supplementary Figure 1 | Schematic illustration of moderate low temperature (MLT, 10°C) stress and TUNEL assay of tapetum program cell death (PCD) in anthers. (A) Schematic illustration of moderate low temperature (MLT, 10°C) stress setup and sampling scheme in cultivar “Micro-Tom.” Six-week-old flowering tomato plants were exposed to MLT-stress for 6 days then moved back to normal temperature for recovery growth. The sample harvested immediately after 6 days MLT-stress were named MLT and harvested from marked tetrad anthers after recovery were named MLTR. Green and yellow lines indicate MLT-stress and NT regimes, respectively. (B) TUNEL assay of tapetum program cell death (PCD) in anther at tetrad, early and late uninucleate and binucleate stages under NT and MLTR conditions. The red signal is propidium iodide staining, and the green fluorescence is TUNEL positive signal. The white arrows indicate TUNEL positive signals. Scale bars = 50 μm.
Supplementary Figure 2 | The expression profiles of writers, erasers and readers. (A) The relative levels of m6A in total RNA of anthers at different stages in NT condition. The levels of m6A in total RNA in stage-I is set to 1. I, anther at microspore mother cell stage; II, anther at tetrad stage; III, anther at early uninucleate stage; IV, anther at late uninucleate stage; V, anther at binucleate stage; VI, anther at mature pollen stage. Each value is the mean ± SD (n = at least 3 biological replicates with 15 plants each). (B) The expression of writers in silico data available from the tomato eFP Browser. RPKM, Reads Per Kilobase per Million mapped reads. (C) The expression of eraser in silico data available from the tomato eFP Browser. (D) The expression of readers in silico data available from the tomato eFP Browser.
Supplementary Figure 3 | m6A-seq data analysis. (A) m6A-seq reads and mapping status with tomato genome in anther at stage-II under NT and MLT conditions. (B) Pearson correlation analysis of m6A-seq. R2 means the square of Pearson correlation. (C) The number of overlapped m6A peak-containing genes identified in three biological replicates in anthers under NT and MLT conditions, respectively. (D) The number of overlapped m6A peak-containing genes between NT and MLT anthers.
Supplementary Figure 4 | KEGG analysis of different enrichment peaks related genes between NT and MLT anthers at stage-II.
Supplementary Figure 5 | Comparative analysis of genes expression levels in NT and MLT conditions. (A,B) The expression levels of SlPYLs and SlPP2Cs genes in anther at stage-II under NT and MLT conditions. The levels of genes expression normalized to Ubiquitin expression are shown relative to the expression of SlPYL2 or SlPP2C1 in NT condition set to 1. Each value is the mean ± SD (n = at least three biological replicates with 15 plants each). ∗P < 0.05; ∗∗P < 0.01 (two-tailed Student’s t- test).
Supplementary Figure 6 | Alignment of AtABCG31 and SlABCG31 full-length proteins. The multiple sequence alignment was generated using Clustal Omega. Same amino acid residues were shading with black color.
Supplementary Table 1 | Primer sequences used in this study.
Supplementary Table 2 | Differential m6A peaks and related transcripts between NT and MLT anthers.
Footnotes
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Keywords: abscisic acid, m6A, moderate low temperature, pollen development, tomato anther
Citation: Yang D, Xu H, Liu Y, Li M, Ali M, Xu X and Lu G (2021) RNA N6-Methyladenosine Responds to Low-Temperature Stress in Tomato Anthers. Front. Plant Sci. 12:687826. doi: 10.3389/fpls.2021.687826
Received: 30 March 2021; Accepted: 12 May 2021;
Published: 04 June 2021.
Edited by:
Kevin Begcy, University of Florida, United StatesReviewed by:
Jing-Ke Weng, Whitehead Institute for Biomedical Research, United StatesMichal Lieberman-Lazarovich, Agricultural Research Organization (ARO), Israel
Copyright © 2021 Yang, Xu, Liu, Li, Ali, Xu and Lu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gang Lu, Z2x1QHpqdS5lZHUuY24=