Front. Plant Sci.

Frontiers in Plant Science

Front. Plant Sci.

1664-462X

Frontiers Media S.A.

10.3389/fpls.2021.727302

Plant Science

Original Research

Identification of Genes and MicroRNAs Affecting Pre-harvest Sprouting in Rice (Oryza sativa L.) by Transcriptome and Small RNAome Analyses

Park

Minsu

¹ ² Choi

Woochang

¹ Shin

Sang-Yoon

¹ Moon

Hongman

¹ Lee

Dowhan

¹ Gho

Yun-Shil

³ Jung

Ki-Hong

³ Jeon

Jong-Seong

³ Shin

Chanseok

¹ ² ⁴ ⁵ ^*

¹Department of Agricultural Biotechnology, Seoul National University, Seoul, South Korea ²Research Center for Plant Plasticity, Seoul National University, Seoul, South Korea ³Graduate School of Biotechnology and Crop Biotech Institute, Kyung Hee University, Yongin, South Korea ⁴Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul, South Korea ⁵Plant Genomics and Breeding Institute, Seoul National University, Seoul, South Korea

Edited by: Won-Gyu Choi, University of Nevada, Reno, United States

Reviewed by: Sibum Sung, University of Texas at Austin, United States; Han Yong Lee, Chosun University, South Korea

*Correspondence: Chanseok Shin, cshin@snu.ac.kr

This article was submitted to Plant Physiology, a section of the journal Frontiers in Plant Science

06 08 2021

2021

727302

18 06 2021 19 07 2021

2021

Park, Choi, Shin, Moon, Lee, Gho, Jung, Jeon and Shin

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.

Pre-harvest sprouting (PHS) is one of the primary problems associated with seed dormancy in rice (Oryza sativa L.). It causes yield loss and reduces grain quality under unpredictable humid conditions at the ripening stage, thus affecting the economic value of the rice crop. To resolve this issue, understanding the molecular mechanism underlying seed dormancy in rice is important. Recent studies have shown that seed dormancy is affected by a large number of genes associated with plant hormone regulation. However, understanding regarding the effect of heat stress on seed dormancy and plant hormones is limited. This study compared the transcriptome and small RNAome of the seed embryo and endosperm of two contrasting japonica rice accessions, PHS susceptible (with low seed dormancy) and PHS resistant (with high seed dormancy), at three different maturation stages. We found that 9,068 genes and 35 microRNAs (miRNAs) were differentially expressed in the embryo, whereas 360 genes were differentially expressed in the endosperm. Furthermore, we identified and verified the candidate genes associated with seed dormancy and heat stress-related responses in rice using quantitative real-time PCR. We newly discovered eight hormone-related genes, four heat shock protein-related genes, and two miRNAs potentially involved in PHS. These findings provide a strong foundation for understanding the dynamics of transcriptome and small RNAome of hormone- and heat stress-related genes, which affect PHS during seed maturation.

rice (Oryza sativa L.) pre-harvest sprouting (PHS) dormancy stress responses transcriptome small RNAome

2019R1A2C1086369

2021R1A5A1032428

National Research Foundation of Korea10.13039/501100003725

�㾩julia��߲��

Introduction

Rice (Oryza sativa L.) is one of the essential crops and the staple food for approximately 50% of the global population (Wei et al., 2013). In the rice field, pre-harvest sprouting (PHS) is crucial issue as it not only reduces the rice grain yield but also significantly affects the grain quality, resulting in a significant economic loss. Under normal conditions, rice seeds can be germinated by controlling their maturation. However, under excess moisture conditions during the period between seed maturation and harvest, the proper seed dormancy is broken, which causes PHS, an important issue that must be overcome to avoid the reduction in grain quality and yield (Gubler et al., 2005). Therefore, understanding the molecular basis of seed dormancy and maturation is crucial for controlling PHS.

Abscisic acid (ABA) plays an important role in the induction and maintenance of seed dormancy (Gubler et al., 2005; Finkelstein et al., 2008; Graeber et al., 2012; Shu et al., 2016). Abscisic aldehyde oxidase 3 (AAO3) catalyzes the final step of ABA biosynthesis. Arabidopsis thaliana mutants aao3-2 and aao3-3 and the rice mutant osao3 exhibit lower seed dormancy and ABA levels than the corresponding wild type (González-Guzmán et al., 2004; Shi et al., 2021). In rice, the basic helix-loop-helix (bHLH) transcription factor gene OsbHLH035 mediates seed germination. The Osbhlh035 mutants showed delayed seed germination and up-regulated OsAAO3 expression (Chen et al., 2018). ABA response and signaling are also involved in seed dormancy. GEM, a member of the GRAM (Glycosyltransferases, Rab-like GTPase Activators, Myotubularins) domain family proteins, is an ABA-responsive protein, and the gem-1 mutant shows increased seed dormancy (Mauri et al., 2016). In rice, the overexpression of the F-box gene, OsFbx352, improves the germination rate of seeds when treated with ABA, and decreases the expression of ABA biosynthesis-related genes (OsNced2 and OsNced3) (Frey et al., 2012; Song et al., 2012).

Ethylene, another plant hormone, promotes seed germination by counteracting ABA signaling (Arc et al., 2013; Corbineau et al., 2014). The metabolic precursor of ethylene, 1-aminocyclopropane-1-carboxylic acid (ACC), produced by ACC synthase (ACS), is oxidized by ACC oxidase (ACO) to form ethylene (Zarembinski and Theologis, 1994; Wang et al., 2002). Transgenic Arabidopsis lines overexpressing the bHLH transcription factor gene PIF5 exhibit up-regulated ACS4 expression and increased ethylene accumulation (Khanna et al., 2007). In addition, aco2 mutants exhibit reduced seed germination via the ACC-mediated reversion of ABA (Linkies et al., 2009). In tomato (Solanum lycopersicum), overexpression of the Ethylene Response Factor 2 (SlERF2) gene results in premature seed germination (Pirrello et al., 2006). On the other hand, the Arabidopsis mutant aterf7 exhibits delayed seed germination and increased ABA sensitivity during seed germination (Song et al., 2005).

In addition to plant hormones, heat shock proteins (HSPs) affect seed dormancy and temperature. Plants synthesize HSPs under high temperature conditions (Kotak et al., 2007; Xue et al., 2014; Muthusamy et al., 2017). Moreover, plants overexpressing HSPs exhibit enhanced heat stress tolerance (Chauhan et al., 2012; Mu et al., 2013; Kaur et al., 2015). In Arabidopsis and tomato, the overexpression of GhHSP24.7, which encodes a small mitochondrial HSP, accelerates seed germination via temperature-dependent generation of reactive oxygen species (Ma et al., 2019). In Arabidopsis, mutation of the AtDjA3 gene (which encodes the J protein, also referred to as HSP40 or DnaJ protein) reduces the germination of seeds when treated with ABA and increases the expression of ABA-INSENSITIVE 3 (ABI3), which is a negative regulator of germination (Parcy et al., 1994; Salas-Muñoz et al., 2016). In rice, overexpression of OsHSP18.2 improves seed germination, and a motif responsible for ABA-inducible expression is present in its promoter (Kaur et al., 2015).

MicroRNAs (miRNAs) regulate the expression of target genes by binding to and cleaving their complementary sequences or inhibiting their translation (Vaucheret, 2006; Axtell, 2013). Furthermore, the biosynthesis and function of miRNAs are regulated by plant hormones and abiotic stress in plants (Reyes and Chua, 2007; Khraiwesh et al., 2012; Sanan-Mishra et al., 2013). However, little is known about miRNAs that regulate PHS, depending on the seed maturation stage.

This study aimed to identify candidate genes and miRNAs that determine the PHS rate in rice.

Materials and Methods Plant Materials and PHS Assay

Two rice (Oryza sativa L. ssp. japonica) accessions, Gopum (PHS susceptible) and Jowoon (PHS resistant), were used in this study. Both accessions were bred in an experimental field of Seoul National University, Suwon, Republic of Korea. Seeds and panicles of Gopum and Jowoon were harvested at 30, 45, and 60 days after heading (DAH). Seeds were sampled by dividing them into embryo and endosperm. To perform the PHS assay, three freshly harvested panicles were incubated at 25°C under 100% relative humidity for 7 days. The number of germinated seeds in each panicle was recorded and expressed as a percentage of the total number of seeds per panicle (Lee et al., 2017). Three replicates were used at each time point. Statistical analyses were performed using the Student’s t-test (^∗P < 0.05; ^∗∗P < 0.01; ^∗∗∗P < 0.001).

Total RNA Extraction and Construction of mRNA and Small RNA Libraries

In total, 10 embryos and endosperms were sampled from one panicle of each plant. Total RNA was extracted from 100 embryos and endosperms, each obtained from 10 plants at three time points (30, 45, and 60 DAH). Briefly, each sample was homogenized in liquid nitrogen using a pestle and mortar and total RNA was then extracted using TRIzol Reagent (Invitrogen, United States), as described previously (Wang et al., 2012). The mRNA libraries were constructed from 2 μg of total RNA using SENSE mRNA-Seq Library Prep Kit V2 for Illumina platforms (LEXOGEN, Austria), based on the manufacturer’s instructions. Small RNAs (18–30 nt) were isolated from 20 μg of total RNA using Urea-PAGE gel, and then small RNA libraries were constructed using Small RNA-Seq Library Prep Kit for Illumina Platforms (LEXOGEN, Austria), based on the manufacturer’s instructions. Four replicates of the mRNA and small RNA samples were prepared.

RNA-Seq Analysis

RNA-seq was performed using the Illumina HiSeq 2500 platform to generate 101-bp paired-end reads. Raw sequences were filtered and trimmed using Trimmomatic v0.3.6. The clean reads were mapped onto the International Rice Genome Sequencing Project (IRGSP) 1.0 reference genome using HISAT2 v2.1.0 with default parameters. The mapped reads were transformed into BAM files using samtools v1.8. The number of mapped reads was quantified using the featureCounts function in Rsubread v2.4.3. To estimate gene expression levels, the mapped read counts were transformed into counts per million (CPM). Subsequently, the CPM values were normalized using the trimmed mean of M-values. The log-transformed CPM values were then used to generate heatmaps with the pheatmap package v1.0.12 in R. Differentially expressed genes (DEGs) with fold-change (FC) ≥ 2 and false discovery rate (FDR) ≤ 0.05 were identified using the edgeR package v3.32.1 by comparing the two rice accessions at each time point.

Gene Ontology Enrichment Analysis

Gene ontology (GO) enrichment analysis was performed to determine the biological roles of the selected genes (Moon et al., 2020). Significantly enriched GO terms were selected with fold enrichment > 2 and FDR < 0.05 using the GO Resource web server.¹

MapMan Analysis

The MapMan software v3.6.0 was used to map the transcriptome data and define functional categories for identifying significantly overrepresented functional genes (Zhang et al., 2020). A dataset containing the IDs of DEGs was constructed with two overviews: regulation and cellular response.

Validation of RNA-Seq Data by Quantitative Real-Time PCR

To validate the RNA-seq data, cDNA was synthesized from each RNA sample using SuperScript III Reverse Transcriptase (Invitrogen, United States), based on the manufacturer’s instructions. Then, quantitative real-time PCR (qRT-PCR) was performed using Light Cycler 480 SYBR Green I Master (Roche, United States) with SYBR Green detection and gene-specific primers. The Ct values for genes were obtained using Os03g0718100 (OsACT1) as a control, and relative expression values were calculated using the ΔΔCt method. Gene-specific primers were designed using NCBI primer BLAST.² The primer sequences of the candidate genes are listed in Supplementary Table 15. Statistical analyses were performed using the Student’s t-test (^∗P < 0.05; ^∗∗P < 0.01; ^∗∗∗P < 0.001).

Small RNA-Seq Data Processing and Differential Expression Analysis of miRNAs

The removal of adaptor sequences and selection of 15–26 nt small RNAs were performed using Cutadapt (v3.4). To obtain high-quality small RNA reads, reads with Phred quality score < 25 were removed using Trimmomatic. The clean reads were then aligned on RNACentral (v.17.0). Oryza sp.-specific non-coding RNA sequences (mostly structural RNAs, including rRNAs, tRNAs, snRNAs, and snoRNAs) were filtered, and the remaining reads were mapped onto the IRGSP-1.0 rice reference genome sequence using bowtie (v1.2.2). To annotate mature rice miRNAs, the IRGSP-mapped small RNA reads were aligned against the mature rice miRNA sequences registered in miRBase (v22) and PmiREN. The filtered read counts were visualized by generating a heatmap using the pheatmap package v1.0.12 in R. Differential expression analysis of miRNAs was performed using edgeR, and miRNAs with log₂FC > 1 and FDR < 0.05 were selected as differentially expressed miRNAs (DEMs).

Results Difference in PHS Rates Between Gopum and Jowoon

We defined three seed maturation stages in this study: early (30 DAH), mid (45 DAH), and late (60 DAH) stages. The PHS rate of Gopum (PHS susceptible accession) was higher than that of Jowoon (PHS resistant accession) at every stage (Figure 1A). In particular, the PHS rate of Gopum was significantly higher than that of Jowoon at 45 DAH by approximately 35-fold (Figures 1B,C). Therefore, we performed RNA-seq and RNAome analyses to identify genes and miRNAs responsible for the difference in the PHS rate between Gopum and Jowoon.

FIGURE 1

Pre-harvest sprouting (PHS) assay in Gopum and Jowoon. (A) PHS phenotypes of Gopum and Jowoon at 30, 45, and 60 days after heading (DAH). The phenotypes before PHS assay (before) and after PHS assay (after) are shown. Scale bar = 5 cm. (B,C) PHS rate of Gopum (B) and Jowoon (C) at 30, 45, and 60 DAH (N = 3). Significance is determined by Student’s t-test, *P < 0.05 and ***P < 0.001.

Identification of DEGs in the Embryo and Endosperm of Gopum and Jowoon

To understand the transcriptional changes in PHS-related candidate genes at different seed maturation stages in Gopum and Jowoon, we performed RNA-seq analysis of the embryo and endosperm at 30, 45, and 60 DAH. After read filtering and trimming, the clean reads were mapped onto the IRGSP 1.0 rice reference genome sequence. The results showed that 16,897 and 14,049 genes were expressed in the embryo and endosperm samples, respectively. The log-transformed CPM values of each gene are depicted as a heatmap in Figures 2A,B.

FIGURE 2

Identification of differentially expressed genes (DEGs) based on the RNA-seq data of the embryo and endosperm of Gopum and Jowoon. (A,B) Heatmaps of expressed genes in the embryo (A) and endosperm (B) of Gopum and Jowoon, respectively. Expressed genes, mapped onto the International Rice Genome Sequencing Project (IRGSP) rice reference genome sequence, are shown as log-transformed counts per million (CPM) values. G30, G45, G60, J30, J45, and J60 indicate Gopum and Jowoon samples at 30, 45, and 60 DAH, respectively. (C,D) Comparison of Gopum and Jowoon based on the number of DEGs in the embryo (C) and endosperm (D). GJ30, GJ45, and GJ60 indicate the comparisons between Gopum and Jowoon at 30, 45, and 60 DAH, respectively. (E,F) Numbers of genes up- or down-regulated in Jowoon compared with those in Gopum in the embryo (E) and endosperm (F) of GJ30, GJ45, and GJ60.

To identify PHS-related candidate genes, gene expression was compared between Gopum and Jowoon samples at 30, 45, and 60 DAH (hereafter referred to as GJ30, GJ45, and GJ60, respectively). In the embryo samples, 2,980, 3,636, and 5,958 DEGs were identified in the GJ30, GJ45, and GJ60, respectively (Figure 2C). In the endosperm samples, no DEG was identified in GJ30, whereas 226 and 215 DEGs were identified in GJ45 and GJ60, respectively (Figure 2D). Genes that were up- or down-regulated in Jowoon compared with those in Gopum in GJ30, GJ45, and GJ60 of embryo and endosperm are shown in Figures 2E,F. Interestingly, the endosperm had significantly less DEGs compared with the embryo. Thus, it is likely that DEGs in the embryo cause the difference in PHS rate between Gopum and Jowoon.

Functional Annotation of DEGs

We performed GO enrichment analysis to predict the biological functions of DEGs in the embryo and endosperm. GO terms in the biological process category with fold enrichment > 2 and FDR < 0.05 were identified. In the embryo samples, DEGs identified in the GJ30, GJ45, and GJ60 were enriched with hormone-related GO terms, such as “response to abscisic acid,” and abiotic stress-related GO terms, such as “response to heat” (Figure 3). In endosperm samples, no significant GO term related to hormones or abiotic stress was identified (Supplementary Tables 7–9). GO term was not identified in the genes down-regulated in Jowoon, compared with those in Gopum of endosperm GJ60. All GO terms in the biological process category are listed in Supplementary Tables 1–9.

FIGURE 3

Gene ontology (GO) enrichment analysis of differentially expressed genes (DEGs) identified in the embryo in the biological process category. (A–C) GO terms (fold enrichment > 2 and false discovery rate < 0.05) of DEGs, which were up- or down-regulated in Jowoon compared with those in Gopum, related to hormones and abiotic stress in the embryo of GJ30 (A), GJ45 (B), and GJ60 (C).

Identification of Hormone- and Abiotic Stress-Related DEGs in the Embryo

High-throughput transcriptome data can be visualized in diverse overviews using the MapMan software, based on multiple omics data of plants (Usadel et al., 2005; Jung and An, 2012). In this study, we used the MapMan software to visualize the function and expression profiles of DEGs at each seed maturation stage in the embryo and endosperm samples of Gopum and Jowoon. The DEGs identified in the embryo (GJ30, GJ45, and GJ60) and endosperm (GJ45 and GJ60) were analyzed using the regulation and cellular response overviews. The hormone-related DEGs identified in the regulation overview, showed the highest changes in indole-3-acetic acid (IAA)-, ABA-, and ethylene-related genes in the embryo of GJ30, GJ45, and GJ60. In addition, in the abiotic stress of the cellular response overview, heat stress-related genes showed the highest expression change in the embryo of GJ30, GJ45, and GJ60 (Figures 4A–C). In the endosperm, no significant changes in hormone− and abiotic stress-related genes were observed in the both GJ45 and GJ60 (Figures 4D,E). These results suggest that IAA−, ABA−, ethylene−, and heat stress-related genes with differential expression between the embryos of Gopum and Jowoon are responsible for the difference in the PHS rate between the two accessions. The regulation and cellular response overviews of all GJ30, GJ45, and GJ60 of embryo and endosperm are shown in Supplementary Figures 1–4.

FIGURE 4

MapMan analysis of differentially expressed genes (DEGs), identified in the embryo and endosperm of Gopum and Jowoon. (A–E) Identification of hormone- and abiotic stress-related DEGs in the embryo of GJ30 (A), GJ45 (B), and GJ60 (C) and in endosperm of GJ45 (D) and GJ 60 (E). The regulation overview and cellular response overview were applied, and the figures were modified from Supplementary Figures 1–4 for DEGs related to hormones and abiotic stress.

Genes Potentially Responsible for the Difference in the PHS Rate Between Gopum and Jowoon

We found that several genes, including AAO, AO, GRAM domain containing gene, bHLH, ACO, ERF, and HSP, were differentially expressed between the embryos of Gopum and Jowoon at 30, 45, and 60 DAH. The review of literature, Rice Annotation Project Database (RAP-DB) and MSU Rice Genome Annotation Project, and related searches revealed several hormone and abiotic stress-related genes with known or expected functions in the embryo (Supplementary Tables 10–12). In addition, we selected PHS-related candidate genes, which have not yet been published. The expression of these genes was validated by qRT-PCR (Figure 5).

FIGURE 5

Relative expression levels of pre-harvest sprouting (PHS)-related candidate genes by quantitative real-time PCR (qRT-PCR). (A) Relative expression levels of abscisic acid (ABA)- and ethylene-related genes. ABA-related genes (top) and ethylene-related genes (bottom) are shown. (B) Relative expression levels of heat shock protein (HSP) genes. Data represent mean ± standard error of mean (SEM; N = 3). Significance is determined by Student’s t-test, *P < 0.05, **P < 0.01, and ***P < 0.001.

Os03g0790900 (OsAAO3), Os03g0790700 (AO), and Os03g0736700 (which contains the GRAM domain) were selected as ABA-related genes, and Os03g0759700 (OsbHLH066), Os02g0771600 (OsACO3), and Os02g0764700 (OsERF103) were selected as ethylene-related genes. Among these genes, Os03g0790900 (OsAAO3) and Os03g0790700 (AO) were up-regulated in Jowoon compared with those in Gopum at 30 and 45 DAH, respectively (Figure 5A). Our results suggest that Os03g0790900 (OsAAO3) and Os03g0790700 (AO) are associated with ABA and affect the low PHS rate of Jowoon at 30 and 45 DAH, respectively. In addition, Os03g0736700 (which contains the GRAM domain), Os03g0759700 (OsbHLH066), Os02g0771600 (OsACO3), and Os02g0764700 (OsERF103) were up-regulated in Gopum compared with those in Jowoon at 30 DAH (Figure 5A). These results suggest that the abovementioned genes are associated with ethylene and affect the higher PHS rate of Gopum compared with that of Jowoon at 45 DAH.

The selected HSP genes including Os01g0135900 (OsHsp17.9B), Os01g0875700 (OsDjB2), Os07g0637150 (which is similar to DnaJ), and Os11g0578100 (OsDjC76) were up-regulated in Gopum compared with those in Jowoon at 30 DAH (Figure 5B). These results suggest that the abovementioned HSP genes are associated with the higher PHS rate of Gopum compared with that of Jowoon at 45 DAH. In addition, the high expression of Os07g0637150 and Os11g0578100 (OsDjC76) at 45 DAH in Jowoon is associated with the PHS of Jowoon seeds at 60 DAH (Figure 5B).

Details of hormone and abiotic stress-related genes in GJ30, GJ45, and GJ60 of the embryo and endosperm, respectively, are summarized in Supplementary Tables 10–14. All primers used for qRT-PCR are listed in Supplementary Table 15.

Identification of PHS-Related Candidate miRNAs and Corresponding Target Genes

On the basis of our transcriptome data, we speculated that the embryo plays a greater role in PHS than the endosperm. Furthermore, we predicted that miRNAs associated with PHS would be expressed in the embryo. To identify miRNAs and their corresponding target genes affecting the difference in PHS rate between Gopum and Jowoon, we performed small RNA-seq analysis of Gopum and Jowoon embryos at 30, 45, and 60 DAH. After read filtering and trimming, the clean small RNA reads were mapped onto the IRGSP 1.0 rice reference genome sequence. The IRGSP-mapped small RNA reads were aligned against the mature rice miRNA sequences in miRBase and PmiREN. Consequently, 2,835 miRNAs were identified in the embryo samples. The heatmap of filtered read counts of miRNAs is shown in Figure 6A. Next, we performed DEM analysis (log₂FC > 1; FDR < 0.05) at each stage to identify PHS-related candidate miRNAs. In total 7, 10, and 26 DEMs were identified in the GJ30, GJ45, and GJ60, respectively (Figure 6B). The up- and down-regulated miRNAs in Jowoon compared with those in Gopum in GJ30, GJ45, and GJ60 are shown in Figure 6C.

FIGURE 6

Identification and expression analysis of differentially expressed miRNAs (DEMs) and the corresponding target genes. (A) Heat map of the expressed miRNAs in the embryo of Gopum and Jowoon. Expressed miRNAs, aligned to miRBase and PmiREN, were shown as filtered read counts (log₂) values. (B) Comparison of Gopum and Jowoon based on the number of DEMs in the embryo of GJ30, GJ45, and GJ60. (C) Number of miRNAs up- or down-regulated in Jowoon compared with those in Gopum in the embryo of GJ30, GJ45, and GJ60. (D,E) Relative expression levels of miRNAs and corresponding target genes, which were predicted to affect PHS. The pairing between miRNAs and their target genes is indicated. The relative expression levels of genes were validated by qRT-PCR. Data represent mean ± SEM (N = 3). Significance is determined by Student’s t-test, *P < 0.05 and **P < 0.01.

The target genes of DEMs were identified using miRNA target gene prediction. We considered the anti-correlation in expression level between DEMs and the corresponding target genes and validated the expression of target genes by qRT-PCR. Subsequently, two miRNAs and two target genes, expected to be associated with PHS, were selected (Figures 6D,E). The osa-miR5827 and osa-miR1862h were expressed at higher levels in Jowoon than in Gopum at all stages, whereas the expression of the corresponding target genes, Os03g0728900 (OsbHLH084) and Os11g0209600 (OsFbox594), respectively, was lower in Jowoon than in Gopum at 30 DAH (Figures 6D,E). These results suggest that Os03g0728900 (OsbHLH084) and Os11g0209600 (OsFbox594) are associated with the higher PHS rate of Gopum compared with that of Jowoon at 45 DAH. In addition, the high expression of osa-miR5827 and osa-miR1862h in Jowoon might be associated with the low PHS rate of Jowoon, especially the case with osa-miR1862h.

The DEMs and their corresponding target genes are summarized in Supplementary Tables 16–18.

Discussion

Rice is one of the most important crops in the world. However, the reduction in rice grain quality and yield due to PHS results in a significant economic loss (Gubler et al., 2005; Wei et al., 2013). Therefore, to overcome PHS, it is necessary to understand the molecular mechanisms underlying seed dormancy and maturation, as well as genes and miRNAs involved in PHS. In this study, we performed RNA-seq and small RNA-seq analyses of the embryo and endosperm tissues of the PHS susceptible accession Gopum and PHS resistant accession Jowoon at three seed maturation stages: 30, 45, and 60 DAH.

Our RNA-seq data revealed the expression of OsSdr4, OsPYL/RCAR5, and OsDOG1L-3, which are well known to negatively control seed germination (Sugimoto et al., 2010; Graeber et al., 2012; Kim et al., 2012; Wang et al., 2020). The expression of Os07g0585700 (OsSdr4) was higher in Jowoon than in Gopum at 60 DAH. In addition, the expression of Os05g0213500 (OsPYL/RCAR5) and Os01g0306400 (OsDOG1L-3) was overall higher in Jowoon than in Gopum; however, no significant expression changes were noted between Gopum and Jowoon based on the seed maturation stages (Supplementary Figure 5).

The results of the GO enrichment and MapMan analyses revealed that hormone- and heat stress-related GO terms and gene expression differences between Gopum and Jowoon were significantly observed in the embryo and rarely in the endosperm (Figures 3, 4 and Supplementary Tables 7–9). These results suggest that the expression of hormone- and heat stress-related genes in embryo plays a crucial role in PHS. Thus, using the embryo data, we identified genes that are expected to affect PHS. We identified three ABA- and three ethylene-related genes. AAO is involved in the last step of ABA biosynthesis. Previously, aao3 and ao3 mutants showed reduced seed dormancy and ABA levels (González-Guzmán et al., 2004; Shi et al., 2021). The expression of Os03g0790900 (OsAAO3) and Os03g0790700 (AO) was higher in Jowoon than in Gopum at 30 and 45 DAH, respectively (Figure 5A). It is possible that the high expression level of Os03g0790900 (OsAAO3) and Os03g0790700 (AO) is associated with high ABA levels in Jowoon seeds at 30 and 45 DAH, respectively, resulting in low PHS rate (Figure 7). GEM, which contains a GRAM domain, is involved in ABA signaling and is activated by ABA, and the Arabidopsis gem-1 mutant shows increased seed dormancy (Mauri et al., 2016). We identified Os03g0736700, which contains a GRAM domain, as a DEG whose expression level was higher in Gopum than in Jowoon at 30 DAH (Figure 5A). We predict that Os03g0736700 responds to ABA and affects the high PHS rate of Gopum after 30 DAH (Figure 7).

FIGURE 7

Proposed model showing the role of ABA, ethylene, and HSPs in seed germination. Red and blue dashed boxes indicate genes expected to positively and negatively regulate the seed germination, respectively. Arrows indicate positive regulation, and bars indicate negative regulation. Bold lines indicate gene functions supported by strong evidence, and dashed lines indicate gene function with limited evidence in seed germination, which requires further investigation.

Ethylene promotes seed germination (Arc et al., 2013; Corbineau et al., 2014). ACS synthesizes the metabolic precursor of ethylene, ACC, which is oxidized by ACO to form ethylene (Zarembinski and Theologis, 1994; Wang et al., 2002). In Arabidopsis, PIF5 overexpression lines showed high ACS4 expression and increased ethylene level (Khanna et al., 2007). In addition, the aco2 mutant showed reduced seed germination (Linkies et al., 2009). The aterf7 mutant showed delayed seed germination, whereas tomato SlERF2 overexpression lines showed early seed germination than the wild type (Song et al., 2005; Pirrello et al., 2006). Os03g0759700 (OsbHLH066, which encodes a bHLH transcription factor), Os02g0771600 (OsACO3), and Os02g0764700 (OsERF103) showed higher expression in Gopum than in Jowoon at 30 DAH (Figure 5A). Therefore, we speculate that these three genes, involved in ethylene biosynthesis and response, contribute to the high PHS rate of Gopum at 45 DAH (Figure 7).

HSPs, associated with ABA, control seed germination. In Arabidopsis and tomato, the overexpression of GhHSP24.7 accelerated seed germination (Ma et al., 2019). In addition, the Atdja3 mutant showed reduced seed germination, when treated with ABA, and higher expression of ABI3 than the wild type (Salas-Muñoz et al., 2016). In rice, an ABA-inducible motif was identified in the OsHSP18.2 promoter region, and OsHSP18.2 overexpression lines showed enhanced seed germination (Kaur et al., 2015). In the present study, Os01g0135900 (OsHsp17.9B) and Os01g0875700 (OsDjB2) showed higher expression in Gopum than in Jowoon at all stages and are, therefore, expected to contribute to the overall high PHS rate of Gopum (Figure 5B). In addition, Os07g0637150 (similar to DnaJ) showed higher expression in Gopum at 30 DAH, whereas Os11g0578100 (OsDjC76) showed higher expression in Jowoon at 45 DAH (Figure 5B). We speculate that these genes are associated with the high PHS rate of Gopum at 45 DAH and that of Jowoon at 60 DAH. On the basis of previous studies (Kaur et al., 2015; Salas-Muñoz et al., 2016), the HSP genes, which showed low expression in Jowoon, may be affected by ABA synthesized from the high expression of Os03g0790900 (AAO3) and Os03g0790700 (AO). These HSP genes may affect the low PHS rate in Jowoon by enhancing the expression of ABI3, which is a negative regulator of seed germination (Figures 5, 7).

We speculate that the difference in the PHS rates of Gopum and Jowoon is caused by the difference in gene expression in the embryo. Little is known about the role of miRNAs in PHS. Therefore, we performed small RNA-seq analysis of the embryo. Using target prediction, we identified F-box and bHLH-related genes as the targets of DEMs from our small RNAome data (Supplementary Tables 16, 17). We selected osa-miR5827, osa-miR1862h, Os03g0728900 (OsbHLH084), and Os11g0209600 (OsFbox594), considering the anti-correlation between miRNA and the corresponding target genes (Figure 6). We speculate that the higher expression of osa-miR5827 and osa-miR1862h in Jowoon and that of Os03g0728900 (OsbHLH084) and Os11g0209600 (OsFbox594) in Gopum at 30 DAH affects the PHS phenotype of the two accessions. In previous studies, PIF5 and the OsbHLH035 were reported to be associated with ethylene biosynthesis (by affecting ACS4 expression) and ABA biosynthesis (by affecting AAO3 expression), respectively (Khanna et al., 2007; Chen et al., 2018). OsbHLH084, which was identified in this study, is expected to be involved in ethylene biosynthesis by affecting the expression of ACS4 or in ABA biosynthesis by lowering the expression of Os03g0790900 (OsAAO3) and Os03g0790700 (AO) in Gopum compared with their expression in Jowoon at 30 and 45 DAH, respectively, leading to the high PHS rate of Gopum after 30 DAH (Figure 7). In addition, on the basis of a previous study (Song et al., 2012), it can be expected that Os11g0209600 (OsFbox594) represses the ABA biosynthesis gene, NCED, and affects the high PHS rate of Gopum after 30 DAH (Figure 7).

Conclusion

In conclusion, by comparing the PHS susceptible rice Gopum with the PHS resistant rice Jowoon, we identified eight hormone-related genes, four HSP-related genes, and two miRNAs as the potential regulators of the difference in PHS between Gopum and Jowoon. In addition, we demonstrated a bioinformatics pipeline that can be used to identify candidate genes and miRNAs involved in PHS; this involves RNA-seq and small RNA-seq analyses and the MapMan analysis of the transcriptome data. A comprehensive review of the previous studies and the results of the present study suggest that interaction between ABA and ABA-related genes and between ABA and HSPs contributes to seed dormancy during seed maturation. On the basis of these results, we propose a model in which seed germination is affected by ABA, ethylene, and HSPs (Figure 7). Additional studies, such as the mutagenesis of hormone-related and HSP genes identified in this study and the measurement of ABA and ethylene contents, are needed to elucidate the interaction between ABA and ABA-related genes, ethylene and ethylene-related genes, and ABA and HSPs. Overall, this study provides big data on the expression dynamics of hormone- and abiotic stress-related genes and miRNAs, which can be utilized in various ways to manipulate seed maturation and PHS.

Data Availability Statement

The original contributions presented in the study are publicly available. The datasets generated and analyzed for this study can be found in the NCBI SRA repository, https://www.ncbi.nlm.nih.gov/sra/, with the GEO accession no. GSE174017 and no. GSE175561.

Author Contributions

CS conceived the research and designed the experiments. MP, DL, J-SJ, and CS planned and performed the field experiments, sampling, and PHS assay. WC, S-YS, HM, Y-SG, and K-HJ performed computational analysis. CS and MP prepared the manuscript. All authors read and approved the manuscript.

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.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Funding. This study was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea Government (MSIT) (Nos. 2019R1A2C1086369 and 2021R1A5A1032428).

We are grateful for the helpful discussions we had with the members of the Shin laboratory. We also thank to Profs. Hee Jong Koh and Sun-Hwa Ha as well as Drs. Su Jang, and Yeon-Hee Lee for their valuable insights on rice sampling.

Supplementary Material

The Supplementary Material for this article can be found online at: /articles/10.3389/fpls.2021.727302/full#supplementary-material

References Arc

Sechet

Corbineau

Rajjou

Marion-Poll

(2013). ABA crosstalk with ethylene and nitric oxide in seed dormancy and germination. Front. Plant Sci. 4:63. 10.3389/fpls.2013.00063

23531630

Axtell

M. J.

(2013). Classification and Comparison of Small RNAs from Plants. Annu. Rev. Plant Biol. 64 137–159. 10.1146/annurev-arplant-050312-120043

23330790

Chauhan

Khurana

Nijhavan

Khurana

J. P.

Khurana

(2012). The wheat chloroplastic small heat shock protein (sHSP26) is involved in seed maturation and germination and imparts tolerance to heat stress. Plant Cell Environ. 35 1912–1931. 10.1111/j.1365-3040.2012.02525.x

22530593

Chen

H.-C.

Cheng

W.-H.

Hong

C.-Y.

Chang

Y.-S.

Chang

M.-C.

(2018). The transcription factor OsbHLH035 mediates seed germination and enables seedling recovery from salt stress through ABA-dependent and ABA-independent pathways, respectively. Rice 11:50. 10.1186/s12284-018-0244-z

30203325

Corbineau

Xia

Bailly

El-Maarouf-Bouteau

(2014). Ethylene, a key factor in the regulation of seed dormancy. Front. Plant Sci. 5:539. 10.3389/fpls.2014.00539

25346747

Finkelstein

Reeves

Ariizumi

Steber

(2008). Molecular Aspects of Seed Dormancy. Annu. Rev. Plant Biol. 59 387–415. 10.1146/annurev.arplant.59.032607.092740

18257711

Frey

Effroy

Lefebvre

Seo

Perreau

Berger

(2012). Epoxycarotenoid cleavage by NCED5 fine-tunes ABA accumulation and affects seed dormancy and drought tolerance with other NCED family members. Plant J. 70 501–512. 10.1111/j.1365-313x.2011.04887.x

22171989

González-Guzmán

Abia

Salinas

Serrano

Rodríguez

P. L.

(2004). Two New Alleles of the abscisic aldehyde oxidase 3 Gene Reveal Its Role in Abscisic Acid Biosynthesis in Seeds. Plant Physiol. 135 325–333. 10.1104/pp.103.036590

15122034

Graeber

Nakabayashi

Miatton

Leubner-Metzger

Soppe

W. J. J.

(2012). Molecular mechanisms of seed dormancy. Plant Cell Environ. 35 1769–1786. 10.1111/j.1365-3040.2012.02542.x

22620982

Gubler

Millar

A. A.

Jacobsen

J. V.

(2005). Dormancy release, ABA and pre-harvest sprouting. Curr. Opin. Plant Biol. 8 183–187. 10.1016/j.pbi.2005.01.011

15752999

Jung

K.-H.

(2012). Application of MapMan and RiceNet drives systematic analyses of the early heat stress transcriptome in rice seedlings. J. Plant Biol. 55 436–449. 10.1007/s12374-012-0270-0 Kaur

Petla

Kamble

Singh

Rao

Salvi

(2015). Differentially expressed seed aging responsive heat shock protein OsHSP18.2 implicates in seed vigor, longevity and improves germination and seedling establishment under abiotic stress. Front. Plant Sci. 6:713. 10.3389/fpls.2015.00713

26442027

Khanna

Shen

Marion

C. M.

Tsuchisaka

Theologis

SchäFer

(2007). The Basic Helix-Loop-Helix Transcription Factor PIF5 Acts on Ethylene Biosynthesis and Phytochrome Signaling by Distinct Mechanisms. Plant Cell 19 3915–3929. 10.1105/tpc.107.051508

18065691

Khraiwesh

Zhu

J.-K.

Zhu

(2012). Role of miRNAs and siRNAs in biotic and abiotic stress responses of plants. Biochim. Biophys. Acta 1819 137–148. 10.1016/j.bbagrm.2011.05.001

21605713

Kim

Hwang

Hong

J.-W.

Lee

Y.-N.

Ahn

I. P.

Yoon

I. S.

(2012). A rice orthologue of the ABA receptor, OsPYL/RCAR5, is a positive regulator of the ABA signal transduction pathway in seed germination and early seedling growth. J. Exp. Bot. 63 1013–1024. 10.1093/jxb/err338

22071266

Kotak

Larkindale

Lee

Von Koskull-Döring

Vierling

Scharf

K.-D.

(2007). Complexity of the heat stress response in plants. Curr. Opin. Plant Biol. 10 310–316. 10.1016/j.pbi.2007.04.011

17482504

Lee

G.-A.

Jeon

Y.-A.

Lee

H.-S.

Hyun

D. Y.

Lee

J.-R.

Lee

M.-C.

(2017). New Genetic Loci Associated with Preharvest Sprouting and Its Evaluation Based on the Model Equation in Rice. Front. Plant Sci. 8:1393. 10.3389/fpls.2017.01393

28848592

Linkies

MuüLler

Morris

TurečKovaì

Wenk

Cadman

C. S. C.

(2009). Ethylene Interacts with Abscisic Acid to Regulate Endosperm Rupture during Germination: a Comparative Approach Using Lepidium sativum and Arabidopsis thaliana. Plant Cell 21 3803–3822. 10.1105/tpc.109.070201

20023197

Guan

Pan

Wang

Liu

(2019). Mitochondrial small heat shock protein mediates seed germination via thermal sensing. Proc. Natl. Acad. Sci. U. S. A. 116 4716–4721. 10.1073/pnas.1815790116

30765516

Mauri

Fernández-Marcos

Costas

Desvoyes

Pichel

Caro

(2016). GEM, a member of the GRAM domain family of proteins, is part of the ABA signaling pathway. Sci. Rep. 6:22660. 10.1038/srep22660

26939893

Moon

Hong

W.-J.

Kim

Y.-J.

Chandran

A. K. N.

Gho

Y.-S.

Yoo

Y.-H.

(2020). Comparative Transcriptome Analysis Reveals Gene Regulatory Mechanism of UDT1 on Anther Development. J. Plant Biol. 63 289–296. 10.1007/s12374-020-09250-w Mu

Zhang

Chen

Liu

(2013). Overexpression of Small Heat Shock Protein LimHSP16.45 in Arabidopsis Enhances Tolerance to Abiotic Stresses. PLoS One 8:e82264. 10.1371/journal.pone.0082264

24349240

Muthusamy

S. K.

Dalal

Chinnusamy

Bansal

K. C.

(2017). Genome-wide identification and analysis of biotic and abiotic stress regulation of small heat shock protein (HSP20) family genes in bread wheat. J. Plant Physiol. 211 100–113. 10.1016/j.jplph.2017.01.004

28178571

Parcy

Valon

Raynal

Gaubier-Comella

Delseny

Giraudat

(1994). Regulation of gene expression programs during Arabidopsis seed development: roles of the ABI3 locus and of endogenous abscisic acid. Plant Cell 6 1567–1582. 10.1105/tpc.6.11.1567

7827492

Pirrello

Jaimes-Miranda

Sanchez-Ballesta

M. T.

Tournier

Khalil-Ahmad

Regad

(2006). Sl-ERF2, a Tomato Ethylene Response Factor Involved in Ethylene Response and Seed Germination. Plant Cell Physiol. 47 1195–1205. 10.1093/pcp/pcj084

16857696

Reyes

J. L.

Chua

N.-H.

(2007). ABA induction of miR159 controls transcript levels of two MYB factors during Arabidopsis seed germination. Plant J. 49 592–606. 10.1111/j.1365-313x.2006.02980.x

17217461

Salas-Muñoz

Rodríguez-Hernández

A. A.

Ortega-Amaro

M. A.

Salazar-Badillo

F. B.

Jiménez-Bremont

J. F.

(2016). Arabidopsis AtDjA3 Null Mutant Shows Increased Sensitivity to Abscisic Acid, Salt, and Osmotic Stress in Germination and Post-germination Stages. Front. Plant Sci. 7:220. 10.3389/fpls.2016.00220

26941772

Sanan-Mishra

Varanasi

S. P. R. M.

Mukherjee

S. K.

(2013). Micro-regulators of auxin action. Plant Cell Rep. 32 733–740. 10.1007/s00299-013-1425-2

23543387

Shi

Tian

Deng

Zhang

Jing

(2021). The rice aldehyde oxidase OsAO3 gene regulates plant growth, grain yield, and drought tolerance by participating in ABA biosynthesis. Biochem. Biophys. Res. Commun. 548 189–195. 10.1016/j.bbrc.2021.02.047

33647795

Shu

Liu

X.-D.

Xie

Z.-H.

(2016). Two Faces of One Seed: hormonal Regulation of Dormancy and Germination. Mol. Plant 9 34–45. 10.1016/j.molp.2015.08.010

26343970

Song

C.-P.

Agarwal

Ohta

Guo

Halfter

Wang

(2005). Role of an Arabidopsis AP2/EREBP-Type Transcriptional Repressor in Abscisic Acid and Drought Stress Responses. Plant Cell 17 2384–2396. 10.1105/tpc.105.033043

15994908

Song

Dai

Zhang

W.-H.

(2012). A rice F-box gene, OsFbx352, is involved in glucose-delayed seed germination in rice. J. Exp. Bot. 63 5559–5568. 10.1093/jxb/ers206

22859682

Sugimoto

Takeuchi

Ebana

Miyao

Hirochika

Hara

(2010). Molecular cloning of Sdr4, a regulator involved in seed dormancy and domestication of rice. Proc. Natl. Acad. Sci. U. S. A. 107 5792–5797. 10.1073/pnas.0911965107

20220098

Usadel

B. R.

Nagel

Thimm

Redestig

Blaesing

O. E.

Palacios-Rojas

(2005). Extension of the Visualization Tool MapMan to Allow Statistical Analysis of Arrays, Display of Coresponding Genes, and Comparison with Known Responses. Plant Physiol. 138 1195–1204. 10.1104/pp.105.060459

16009995

Vaucheret

(2006). Post-transcriptional small RNA pathways in plants: mechanisms and regulations. Genes Dev. 20 759–771. 10.1101/gad.1410506

16600909

Wang

Zhang

Wang

Song

(2012). Isolation of High Quality RNA from Cereal Seeds Containing High Levels of Starch. Phytochem. Anal. 23 159–163. 10.1002/pca.1337

21739496

Wang

K. L. C.

Ecker

J. R.

(2002). Ethylene Biosynthesis and Signaling Networks. Plant Cell 14 S131–S151. 10.1105/tpc.001768

12045274

Wang

Lin

Duan

Huang

Yang

(2020). OsDOG1L-3 regulates seed dormancy through the abscisic acid pathway in rice. Plant Sci. 298:110570. 10.1016/j.plantsci.2020.110570

32771171

Wei

F.-J.

Droc

Guiderdoni

Hsing

Y.-I. C.

(2013). International Consortium of Rice Mutagenesis: resources and beyond. Rice 6:39. 10.1186/1939-8433-6-39

24341871

Xue

G.-P.

Sadat

Drenth

McIntyre

C. L.

(2014). The heat shock factor family fromTriticum aestivumin response to heat and other major abiotic stresses and their role in regulation of heat shock protein genes. J. Exp. Bot. 65 539–557. 10.1093/jxb/ert399

24323502

Zarembinski

T. I.

Theologis

(1994). Ethylene biosynthesis and action: a case of conservation. Plant Mol. Biol. 26 1579–1597. 10.1007/bf00016491

7858205

Zhang

Shi

Shan

Zhao

Huang

(2020). Analysis of the Transcriptome of Polygonatum odoratum (Mill.) Druce Uncovers Putative Genes Involved in Isoflavonoid Biosynthesis. J. Plant Biol. 63 217–228. 10.1007/s12374-020-09246-6

http://geneontology.org

http://www.ncbi.nlm.nih.gov/tools/primer-blast/

�㾩julia�������߲���

�㾩julia��߲��