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The phytohormone abscisic acid (ABA) plays important roles in the induction and maintenance of seed dormancy. Although application of exogenous ABA inhibits germination, the effects of exogenous ABA on ABA-mediated gene transcription differ from those of endogenous ABA. To understand how endogenous ABA regulates the transcriptomes in seeds, we performed comprehensive expression analyses using whole-genome Affymetrix tiling arrays in two ABA metabolism mutants – an ABA-deficient mutant (aba2) and an ABA over-accumulation mutant (cyp707a1a2a3 triple mutant). Hierarchical clustering and principal components analyses showed that differences in endogenous ABA levels do not influence global expression of stored mRNA in dry seeds. However, the transcriptome after seed imbibition was related to endogenous ABA levels in both types of mutant. Endogenous ABA-regulated genes expressed in imbibed seeds included those encoding key ABA signaling factors and gibberellin-related components. In addition, cohorts of ABA-upregulated genes partially resembled those of dormant genes, whereas ABA-downregulated genes were partially overlapped with after-ripening-regulated genes. Bioinformatic analyses revealed that 6105 novel genes [non-Aradopsis Genome Initiative (AGI) transcriptional units (TUs)] were expressed from unannotated regions. Interestingly, approximately 97% of non-AGI TUs possibly encoded hypothetical non-protein-coding RNAs, including a large number of antisense RNAs. In dry and imbibed seeds, global expression profiles of non-AGI TUs were similar to those of AGI genes. For both non-AGI TUs and AGI code genes, we identified those that were regulated differently in embryo and endosperm tissues. Our results suggest that transcription in Arabidopsis seeds is more complex and dynamic than previously thought.
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Germination is a critical event for survival and reproductive success in the plant life cycle. Therefore, seed dormancy is an adaptive trait in unfavorable conditions. Primary dormancy is acquired during seed maturation and is broken during storage of dry seeds, i.e. at after-ripening (Karssen et al., 1983). After-ripened seeds enter a secondary dormant state in unfavorable germination conditions. In most plant species, seed dormancy and germination are controlled by several environmental factors such as light, temperature, nutrients and other seed storage conditions (Baskin and Baskin, 1998). Many environmental factors alter the metabolism and signaling of two plant hormones, abscisic acid (ABA) and gibberellins (GAs) (Finkelstein et al., 2008; Holdsworth et al., 2008). Abscisic acid promotes the induction and maintenance of seed dormancy, whereas GA is required for the initiation and completion of germination. It is thought that germination is regulated by the antagonistic effects of ABA and GA.
In typical angiosperm seeds, germination is controlled by both the growth potential of the embryo and the restrictive potential of tissues surrounding it. Embryo growth is triggered by increasing the pressure potential and extensibility of the cell wall. These changes allow protrusion of the radicle, which marks the completion of germination (Bewley, 1997). Abscisic acid arrests embryo growth by inhibiting the extensibility of the embryonic cell wall (Schopfer and Plachy, 1985; da Silva et al., 2004). On the other hand, the endosperm and testa tissues surrounding the embryo act as a mechanical barrier to germination (Bewley, 1997; Muller et al., 2006). Although the testa is a dead tissue in imbibed seeds, abnormal testa mutants in Arabidopsis (Arabidopsis thaliana) show a reduced dormancy phenotype, indicating that testa components contribute to seed dormancy and germination (Debeaujon and Koornneef, 2000; Léon-Kloosterziel et al., 1994). In contrast, endosperm is a living tissue in Arabidopsis and produces enzymes related to cell wall modification. Activity of these enzymes is induced in response to GA prior to germination (Halmer et al., 1976; Chen and Bradford, 2000; Nonogaki et al., 2000; Wu et al., 2001). Interestingly, endosperm weakening is also antagonistically regulated by ABA and GA in cress (Lepidium sativum), a close relative of Arabidopsis (Muller et al., 2006).
In many cases, high levels of endogenous ABA are associated with physiologically dormant states. Levels of ABA change drastically during seed development and seed imbibition in response to developmental and environmental cues. The ABA accumulated during maturation is essential for inducing and maintaining seed dormancy (Karssen et al., 1983; Koornneef et al., 1989). Therefore, freshly harvested seeds of ABA-deficient mutants of Arabidopsis, tomato (Lycopersicon esculentum) and tobacco (Nicotiana plumbaginifolia) fail to induce lasting seed dormancy (Karssen et al., 1983; Groot and Karssen, 1992; Grappin et al., 2000). In several plant species, imbibed dormant seeds accumulate more ABA than imbibed non-dormant seeds (Grappin et al., 2000; Jacobsen et al., 2002; Ali-Rachedi et al., 2004). Seed dormancy is maintained via activation of de novo ABA biosynthesis after seed imbibition. Thus, seeds of ABA biosynthesis mutants can germinate in unfavorable conditions, such as darkness after irradiance of far-red light, high temperature and high salinity (González-Guzmán et al., 2004; Seo et al., 2006; Tamura et al., 2006). In contrast, activation of ABA catabolism is enhanced by after-ripening in imbibed seeds, and the levels of ABA decrease and remain at low levels until germination (Millar et al., 2006). Therefore, ABA catabolism is one of the factors that regulate seed dormancy and germination.
Genetic screening by application of exogenous ABA has identified a large number of ABA signaling factors associated with seed dormancy and germination. Several protein phosphatase 2Cs (e.g. ABI1, ABI2, AHG1 and AHG3) and transcription factors (e.g. ABI3, ABI4, ABI5 and CHO1) are key components in the ABA signal transduction pathway (Finkelstein et al., 2008; Holdsworth et al., 2008; Yamagishi et al., 2009). Application of exogenous ABA to imbibed seeds is useful for identification of ABA signaling components and experimental manipulation to mimic dormancy states. Indeed, exogenous ABA can reduce germination potential and delay endosperm rupture in non-dormant Arabidopsis seeds (Chibani et al., 2006; Muller et al., 2006). Moreover, exogenous ABA repressed the expression of a GA biosynthesis gene in the embryo of sorghum (Sorghum bicolor) (Pérez-Flores et al., 2003). In contrast, it has been pointed out that application of exogenous ABA to non-dormant seeds does not reflect transcriptome and proteome levels in dormant seed states (Chibani et al., 2006; Carrera et al., 2008). For example, metabolic and physiological processes in seeds treated with exogenous ABA differ from those of dormant seeds (Pritchard et al., 2002; Penfield et al., 2004; Muller et al., 2006).
To date, transcriptome data from Arabidopsis seeds in various different physiological states have been obtained using Affymetrix ATH1 arrays. These data are available from the Arabidopsis eFP Browser (Winter et al., 2007). Although they are useful, recent transcriptome analyses have revealed that in Arabidopsis there are a large number of novel transcripts including non-protein-coding RNAs (Yamada et al., 2003; Stolc et al., 2005; Zhang et al., 2006; Matsui et al., 2008; Zeller et al., 2009; Hazen et al., 2009). To understand how endogenous ABA controls seed dormancy and germination, we performed comprehensive transcriptome analyses of ABA-deficient and ABA over-accumulation mutants using whole-genome Affymetrix tiling arrays. In addition, we also compared the transcriptome profiles between embryo and endosperm tissues to understand tissue-specific expression patterns. We characterized the expression patterns of both Arabidopsis Genome Initiative (AGI) code genes and novel genes (non-AGI transcriptional units) including a large number of non-protein-coding RNAs in Arabidopsis seeds.
Result and discussion
Control of seed dormancy and germination by endogenous ABA
In many plant species determination of seed dormancy and germination is related to the endogenous ABA levels, which are controlled by a combination of ABA biosynthesis and catabolism (Nambara and Marion-Poll, 2005). A key enzyme in ABA catabolism, CYP707A, was reported to be important for breaking seed dormancy (Kushiro et al., 2004; Millar et al., 2006; Okamoto et al., 2006). However, seed dormancy of cyp707a single and double mutants is completely broken by stratification or after-ripening for a short period (Okamoto et al., 2006). To find out if CYP707A contributes to breaking seed dormancy, we generated a triple mutant defective in CYP707A1, CYP707A2 and CYP707A3. The ABA levels in dry seeds of the cyp707a1a2a3 triple mutant were 70-fold higher than those in the wild type and remained at high levels after seed imbibition (Figure 1a). This over-accumulation of ABA was more prominent in the cyp707a1a2a3 triple mutant than in cyp707a double mutants (Okamoto et al., 2006). Freshly harvested cyp707a1a2a3 triple-mutant seeds did not germinate at 22°C after stratification for 3 days (Figure 1b,c). In addition, a long period of dry storage (6 months) could not rescue hyper-dormancy of the cyp707a1a2a3 triple-mutant seeds. Seed dormancy of the cyp707a1a2a3 triple mutant is stronger than that of Cape Verde Islands (Cvi), a dormancy accession of Arabidopsis, because Cvi seeds germinated after 6 months of dry storage in our conditions (Figure S1 in Supporting Information). A previous study showed that the cyp707a1a2 double mutant was hyper-dormant, but this dormancy was easily released by after-ripening. The present results demonstrate that ABA 8′-hydroxylases are essential for regulating seed dormancy, and loss of function of the three CYP707A genes led to prominent dormancy, which was not easily released by after-ripening. In fact, germinating seeds showed high levels of CYP707A expression while non-germinating seeds did not (Millar et al., 2006; Toh et al., 2008). It is worth mentioning that seed dormancy of the cyp707a1a2a3 triple mutant was broken by a combination of after-ripening and stratification or GA treatment (Figure 1c). It is possible that dormancy release in the cyp707a1a2a3 triple mutant is accomplished by an ABA 8′-hydroxylase-independent mechanism, for example the ABA conjugate pathway, decreased ABA sensitivity or increased GA sensitivity and/or biosynthetic ability. On the other hand, de novo ABA biosynthesis is required to maintain seed dormancy after seed imbibition. Therefore, the ABA biosynthesis mutant aba2 showed a lesser degree of seed dormancy than the wild type as reported previously (Figure 1a,b; Léon-Kloosterziel et al., 1996).
Next, we examined whether endogenous ABA levels correlate with transcript levels of ABA-responsive and signaling-related genes. In Arabidopsis seeds, ABI4, ABI5, AHG1 and AHG3 are involved in ABA signal transduction, whereas AtEM6 and RD29B are ABA-responsive genes. Interestingly, in dry seeds, transcript levels of these genes did not differ remarkably between the wild type and the mutants (Figure 2). However, after seed imbibition, transcript levels of these genes reflected endogenous ABA levels (Figure 2). In 12, 24 and 36-h imbibed seeds, transcript levels of ABI5, AtEM6, RD29B, AHG1 and AHG3 were higher in the cyp707a1a2a3 triple mutant and lower in the aba2 mutant, compared with those in the wild type (Figure 2). On the other hand, induction of ABI4 in the cyp707a1a2a3 triple mutant was repressed compared with that in the aba2 mutant and wild-type after seed imbibition (Figure 2). Application of exogenous (+)-S-ABA (3 μm) inhibited germination of freshly harvested wild-type seeds (data not shown), but its effect on gene expression was relatively minor at early seed imbibition. Transcript levels of AHG3 and RD29B, but not ABI5, AHG1 and AtEM6, in the wild type treated with exogenous ABA were slightly higher than those in the control at 24 h after seed imbibition. Application of exogenous ABA to after-ripened seeds does not mimic dormant seed states with respect to transcriptomic and proteomic traits (Chibani et al., 2006; Carrera et al., 2007). In addition, exogenous ABA cannot completely prevent catabolism of fatty acids or lipids, which is necessary for embryo and seedling growth during germination (Pritchard et al., 2002; Penfield et al., 2004). Our expression analyses indicate that exogenous ABA markedly affected the expression of several genes at a later stage, in particular RD29B (Figure 2).
Global expression profiling in seeds by tiling array analysis
To reveal the global transcription profiles regulated by endogenous ABA in Arabidopsis seeds, we carried out comprehensive transcriptome analyses of aba2 and cyp707a1a2a3 triple mutants using whole-genome tiling arrays. We also examined tissue-specific transcript accumulation in embryo and endosperm tissues, because interactions between these tissues are a key process in the control of seed dormancy and germination. Total mRNA was extracted from whole dry seeds and 24-h imbibed seeds of the wild type and mutants (aba2 and cyp707a1a2a3 triple mutant). We also extracted total mRNA from dissected embryo and endosperm tissues of wild-type seeds after 24-h imbibition. Biotin-labeled cRNAs were hybridized to the whole-genome tiling array set (1.0 F array and 1.0 R array, Affymetrix, http://www.affymetrix.com/).
Tiling array data were analyzed based on the TAIR8 gene model, and the signal intensity of an AGI code gene was calculated by using the Arabidopsis tiling array-based detection of exons (ARTADE) method (Toyoda and Shinozaki, 2005; Matsui et al., 2008). Of a total of 32 144 AGI code genes, 18 848 genes were expressed in at least one condition (P initial value <10−8) (Table S1). The 18 848 expressed AGI code genes were analyzed using hierarchical clustering analysis (Figure 3a). There were large differences in endogenous ABA levels among the various seed types. However, in dry seeds, transcript levels of AGI code genes were similar among the wild -type, aba2 and cyp707a1a2a3 triple mutant (Figure 3a). After seed imbibition, the global expression patterns of these mutants drastically differed from that of the wild type (Figure 3a). These expression patterns indicate that endogenous ABA levels affect global transcription in association with seed dormancy and germination states after seed imbibition rather than dry seed states. Moreover, the global expression patterns in embryo and endosperm differed from that of imbibed whole wild-type seeds. This result indicates that the transcriptome of seeds is made up of integrated transcriptomes from the embryo and thin endosperm layers. In other words, although the endosperm is a thin single-celled layer in Arabidopsis seeds, expression of endosperm-specific genes contributes to global expression of imbibed whole seeds.
To further compare these transcriptomes, 15 331 differentially expressed AGI code genes (P initial value <10−8; false discovery rate (FDR) α = 0.05; Table S2) in at least one condition were analyzed using a principal components analysis (PCA). Dry seeds of the wild type, the aba2 mutant and the cyp707a1a2a3 triple mutant were located at similar positions, suggesting that these seeds are similar at the transcriptome level compared with imbibed seeds (Figure 3b). Interestingly, the position on the first PCA axis of 24-h imbibed seeds of the cyp707a1a2a3 triple mutant was located close to that of dry seeds, whereas the positions of 24-h imbibed wild-type and aba2 mutant seeds were located distantly from that of dry seeds. From these observations, the first dimension (PC1) is likely to reflect dormancy or germination states. Indeed, LEA and RD29B genes were observed in low scores on the first PCA axis (Table S2). These genes are expressed at high levels in dry or dormant seeds (Bassel et al., 2008; Carrera et al., 2008). Conversely, several 40S and 60S ribosomal protein genes, which are indicators of growth status, were observed in high scores on the first PCA axis (Tatematsu et al., 2008; Table S2). The second dimension (PC2) is likely to reflect the differences between embryo and endosperm. As reported previously, genes related to protein metabolism were observed in high scores (Penfield et al., 2006; Table S2). In contrast, a large number of pentatricopeptide repeat (PPR) proteins and RNA metabolism-related genes were observed in low scores in PC2 (Table S2). The PPR proteins have a range of essential functions in post-transcriptional processing of RNA in mitochondria and chloroplasts (Schmitz-Linneweber and Small, 2008). A subset of mutants of PPR genes show embryo-defective phenotypes or severely reduced germination, indicating that these proteins are required for normal embryo growth (Lurin et al., 2004; de Longevialle et al., 2007).
Gene expression analysis in aba2 and cyp707a1a2a3 triple mutants
As shown in Figure 2, expression of ABA-responsive and signaling-related genes is associated with endogenous ABA levels in the aba2 mutant and the cyp707a1a2a3 triple mutant. To identify ABA-responsive AGI code genes, significant differences were judged by the Mann–Whitney U-test (FDR α = 0.05; Storey, 2002; Storey and Tibshirani, 2003). In dry seeds, there were few genes showing an opposite expression pattern between the aba2 mutant and cyp707a1a2a3 triple mutant (i.e. an expression ratio for aba2/wild type >2.0 and cyp707a1a2a3/wild type <2.0; Figure S2 and Table S3). This result suggests that a large number of stored mRNAs in dry seeds might be regulated by independent mechanisms in these mutants. It was also reported that the global expression patterns were similar among dry seeds of the wild type and two ABA-insensitive mutants, abi4 and abi5 (Nakabayashi et al., 2005). However, severely ABA-insensitive mutants, such as abi3-6 or snrk2d/e/i triple mutants, cannot enter seed maturation processes, and numerous genes in these dry seeds showed different transcript levels from those in the wild-type seeds (Nakashima et al., 2009). From these results, a large number of stored mRNAs might be predominantly regulated by the threshold of ABA sensitivity concurrent with the developmental signal rather than endogenous ABA levels, because the seeds of the ABA metabolism-related mutants, aba2 and cyp707a1a2a3, can progress towards seed maturation in a similar manner as wild-type seeds. However, it is worth mentioning that many photosynthesis- and cell wall-related genes were observed among the upregulated genes of the aba2 dry seeds (Table S3). These genes are known as feature genes that are expressed during germination. This observation indicates that endogenous ABA levels are required for repressing the expression of these genes during the seed maturation process. In contrast to dry seeds, at 24 h after seed imbibition we identified 336 ABA-upregulated genes, including ABA signaling factors, ABI5, AHG1, ATAF1 and EEL, and a regulator of ABA and GA metabolism, SOMNUS (Figure 4a and Table S3). As expected, CACGTG-related sequences, one of the most typical ABA-responsive elements, were frequently observed in the 0.5-kb upstream regions of 335 ABA-upregulated AGI genes (Table S4; Shen and Ho, 1995). We also identified 586 ABA-downregulated AGI code genes at 24 h after seed imbibition, including the GA metabolism-related genes GA3ox1 and GA3ox2 and their regulator SPATULA (Figure 4a and Table S3). Indeed, expression of GA3ox1 and GA3ox2 is repressed by elevated endogenous ABA in unfavorable conditions (Seo et al., 2006; Toh et al., 2008).
To understand how ABA-responsive genes affect biological processes in seeds, we used TAGGIT ontology, which is a seed biology-related gene ontology (GO) annotation (Carrera et al., 2007). TAGGIT ontology analysis revealed that seed storage proteins and dormancy-related genes were only observed among the ABA-upregulated genes (Table S5). Genes associated with photosynthesis, glycolysis and gluconeogenesis, cell wall modification, the cell cycle and the Krebs cycle were more commonly found among the ABA-downregulated genes than among ABA-upregulated genes (Table S5). From these observations, cohorts of ABA-upregulated and -downregulated genes possibly reflected those of dormant and after-ripened states, respectively (Carrera et al., 2007). Therefore, our ABA-responsive gene list was compared with dormancy or after-ripened genes as reported previously (Cadman et al., 2006). Among 586 ABA-downregulated genes, 57 genes, including GA3ox1 and SPATULA, were overlapped with after-ripened genes, whereas GA3ox2, an ABA-downregulated gene, was not among the after-ripened genes (Figure 4b and Table S6). On the other hand, of 336 ABA-upregulated genes, 95 genes including EEL, ATAF1, RD29B, LEAs, AtEM1 and AtEM6, overlapped with dormancy genes but not after-ripened genes (Figure 4c and Table S6). Interestingly, two major ABA signaling factors in Arabidopsis seeds, ABI5 and AHG1, were not included among the dormancy genes, suggesting that seed dormancy might be regulated by a different pathway of ABA signal transduction. It is reported that the abi5 mutant exhibits a similar degree of seed dormancy as the wild type (Finkelstein, 1994). In contrast, the abi5 mutant can germinate in the presence of a GA biosynthesis inhibitor (Piskurewicz et al., 2008). In the case of secondary seed dormancy at high temperatures, only a subset of ABA signaling factors is involved in thermoinhibition of Arabidopsis seed germination (Tamura et al., 2006). Consistent with our speculation, these observations imply that seed dormancy is controlled by various ABA signaling factors that respond to multiple external cues.
We have identified many ABA-responsive genes using ABA-deficient and ABA-overaccumulation mutants. However, we also cannot exclude the possibility that part of these genes is regulated by developmental transition, because endogenous ABA levels are generally associated with seed dormancy and germination states. Therefore, it appears that ABA-responsive genes are composed of ones directly regulated by ABA and ones regulated by both ABA and developmental transition.
Embryo- and endosperm-specific expression of regulators for seed dormancy and germination
Tiling array analyses using dissected embryo and endosperm tissues revealed that 16 094 AGI code genes were expressed in these tissues at 24 h after seed imbibition (P initial value <10−8; Table S1). ABI4 was predominantly expressed in the embryo (for embryo, 10 463; for endosperm, 1526; P-value <0.0001), whereas AtEPR1 was almost exclusively expressed in the endosperm (for embryo, 918; for endosperm, 86 944; P-value <0.0001). This result indicates that there was no significant cross-contamination between the two fractions. The Mann–Whitney U-test (FDR α = 0.05; signal value cut-off twofold difference) revealed that 1657 genes, including embryo-specific markers, PDF1, ABI4, GA3ox1 and GA3ox2, were predominantly expressed in embryo tissues (Figure 4d and Table S7). It is worth mentioning that the ABA-upregulated genes, EEL and AtEM1, and the ABA-downregulated genes, GA3ox1 and GA3ox2, were predominantly expressed in the embryo, suggesting that endogenous ABA regulates their transcription in specific tissues (Figure 4e). TAGGIT ontology analysis revealed that more genes related to DNA repair/RNA metabolism, respiration and photosynthesis were expressed in the embryo than in the endosperm (Table S5). Notably, a subset of mutants in mRNA metabolism-related genes show embryo-defective or seedling-lethal phenotypes (SeedGenes Project, http://www.seedgenes.org/). Interestingly, seeds of a mutant lacking mRNA processing-related components exhibit an ABA-hypersensitive phenotype (Finkelstein et al., 2008). A large number of mRNA species change drastically during germination in association with ABA levels (Ogawa et al., 2003; Nakabayashi et al., 2005). Therefore, ABA is likely to be involved in tissue-specific expression patterns of these genes.
On the other hand, we identified 1734 genes including endosperm-specific markers, AtEPR1 and MYB10, that were expressed in the endosperm rather than the embryo (Figure 4d,e and Table S7). AtEPR1 is expressed in the endosperm during germination (Dubreucq et al., 2000). Our study revealed that this gene was highly expressed even in cyp707a1a2a3 triple mutants after seed imbibition. It is possible that AtEPR1 affects the composition of the cell wall in the endosperm and contributes to maintenance of dormant seeds. Indeed, AtEPR1 expression is observed from late-maturation to mature dry seeds, and its expression levels are maintained in dormant seeds rather than non-dormant seeds (Schmid et al., 2005; Cadman et al., 2006; Bassel et al., 2008). Among ABA-downregulated genes, expression of SPATULA and the cell wall-related genes ATXTH17 and ATXTH18 was higher in the endosperm than in the embryo (Figure 4e). These genes are probably involved in endosperm weakening during germination. TAGGIT ontology analysis revealed that the Krebs cycle, β-oxidation and stress-related genes were more abundant in the endosperm than in the embryo (Table S5). Mobilization of endosperm lipid reserve by the Krebs cycle and β-oxidation is important for embryo growth during germination (Penfield et al., 2004, 2006). Stress-related genes included the flavonoid biosynthetic enzymes TT6 and TT7 (Table S5). Most tt mutants show reduced dormancy, and tt7 mutants were also isolated as resistant to high temperature and germinating at cold temperatures, indicating that flavonoid biosynthesis contributes to the regulation of germination (Debeaujon and Koornneef, 2000; Salaita et al., 2005; Tamura et al., 2006).
Penfield et al. (2006) has reported transcriptome analysis of embryo and endosperm in Arabidopsis. Therefore, a list of the embryo- and endosperm-specific genes identified in this study was compared with that of Penfield et al. (2006). About 40% of our embryo- and endosperm-specific genes overlapped with the previous data set (Figure S3 and Table S8). This low percentage of overlap might be due to differences in the preparation of the seed materials, i.e. in this study, the data set was obtained from 24-h imbibed seeds without stratification, whereas the Penfield data set was obtained from 24-h imbibed seeds after 3 days of stratification.
Identification and characterization of novel transcriptional units in Arabidopsis seeds
Next, we focused on the novel transcriptional units (TUs; i.e. non-AGI TUs) in the TAIR8 gene model, because the tiling array can detect all transcripts from the entire genome. We identified 6105 non-redundant groups of non-AGI TUs (Table S9) as the expressed ones using the ARTADE method (P initial value <10−8) (Toyoda and Shinozaki, 2005). These non-AGI TUs were located across the whole chromosome similarly to AGI code genes (Figure S4). Among non-AGI TUs, 706 (11.6%) and 3333 (55.6%) were overlapped with Arabidopsis community full-length cDNAs, including RIKEN full-length cDNAs and reliable signatures of massively parallel signature sequencing (MPSS) tag sequences, respectively (Figure S4 and Table S9; Seki et al., 2002; Meyers et al., 2004). Furthermore, 2517 (41.2%) non-AGI TUs were novel, and 3588 (58.8%) non-AGI TUs were previously identified as the non-AGI TUs expressed in Arabidopsis seedlings under stress or exogenous ABA treatment (Figure 5a; Matsui et al., 2008). Interestingly, 5900 (97%) non-AGI TUs did not have sequence similarity with any proteins in the National Institutes of Health data set (Table S9). This result suggests that these non-AGI TUs probably encode hypothetical non-protein-coding RNA. In addition, 5256 (86%) and 849 (14%) of the non-AGI TUs were defined as antisense and intergenic types, respectively (Figure 5b,d,e and Table S9). In the case of protein-coding non-AGI TUs, approximately 50% of TUs were expressed in intergenic regions, and their sequence similarities were moderately conserved in the expressed sequence tag (EST) data sets from other plant species in the NCBI Unigene database (Figure 5b,c, Tables S9 and S10). In contrast, non-protein-coding non-AGI TUs in intergenic regions were less conserved than protein-coding TUs (Figure 5c and Table S10), suggesting that non-protein-coding TUs have evolved more rapidly than protein-coding TUs.
Expression of these non-AGI TUs was also analyzed by using strand-specific RNA probes. The expression of non-AGI TUs was observed in dry seeds and/or imbibed seeds (Figure 6a,b). These results indicate that non-AGI TUs are not artifacts in tiling array experiments and are expressed in Arabidopsis seeds. In northern analyses, the sense and antisense transcripts showed similar expression patterns, except for At1g05190/SG0123 (Figure 6a). There was a linear correlation between sense and antisense transcripts of 5705 AGI/non-AGI TU pairs (r =0.64) but not between those of 1435 AGI/AGI pairs (r =6.3 × 10−4) (Figure S5 and Table S11). We also detected antisense transcripts for many major ABA-related genes including AHG1, ABI5, RD29B and AtEM6, which were downregulated after seed imbibition similarly to sense transcripts (Table S11). A linear correlation between expression of AGI/non-AGI TUs was also observed in stress responses (Matsui et al., 2008). Recently, Hazen et al. (2009) reported that the expression patterns of some antisense transcripts differed from those of sense transcripts in circadian clock regulation. These observations suggest that antisense transcripts might be regulated dynamically in response to periodic changes in the environment. Interestingly, there was also a linear correlation (r =0.61) between the 123 non-AGI/non-AGI TU pairs, as reported previously (Figure S5; Matsui et al., 2008). Indeed, expression patterns of the pairs SG1645/SG1646 and SG3258/SG3259 were similar during seed imbibition (Figure 6b).
Expression of non-AGI TUs in seeds
We performed a hierarchal clustering analysis on 6105 non-AGI TUs (Figure 7a). Expression patterns of non-AGI TUs in dry seeds were similar among the wild type, the aba2 mutant and the cyp707a1a2a3 triple mutant (Figure 7a). However, after seed imbibition there were significant differences in expression patterns of many non-AGI TUs among the three types. Moreover, expression patterns of non-AGI TUs in embryos differed from those in endosperm tissues. In fact, ABA-responsive non-AGI TUs in dry seeds were barely identified by the Mann–Whitney U-test (Figure S6 and Table S12). On the other hand, we identified 42 ABA-upregulated and three ABA-downregulated non-AGI TUs at 24 h after seed imbibition (Figure 7b and Table S12), whereas expression of 61 and 775 non-AGI TUs was identified as embryo- and endosperm- specific in 24-h imbibed seeds, respectively (Figure 7c and Table S13). A RT-PCR expression analysis was performed to confirm ABA-responsive and tissue-specific expression of several non-AGI TUs in intergenic regions. In agreement with tiling array data, after seed imbibition, expression of ABA-responsive non-AGI TUs was associated with endogenous ABA levels, and expression of tissue-specific non-AGI TUs depended on the tissues used (Figure 7d,e and Tables S12 and S13). Notably, ABA-upregulated SG1158 and SG3065 and ABA-downregulated SG3872 were predominantly expressed in the endosperm (Figure 7d,e). These results indicate that expression of stored non-AGI TUs in dry seeds is hardly influenced by endogenous ABA levels, and that the expression patterns of ABA-responsive and tissue-specific non-AGI TUs after seed imbibition are similar to those of AGI genes. However, significantly fewer ABA-responsive non-AGI TUs were expressed compared with ABA-responsive AGI code genes in 24-h imbibed seeds. These results imply that the changes in expression patterns of non-AGI TUs are less dynamic than those of AGI code genes after seed imbibition (Figure S5).
Recent transcriptome studies have shown that many mRNAs resembling non-protein-coding RNA are present in addition to microRNAs and small interfering RNAs in Arabidopsis and rice (Oryza sativa) (Li et al., 2006; Zhang et al., 2006; Matsui et al., 2008). We also have found more than 5900 non-protein-coding RNAs in Arabidopsis seeds in this study. Although the functions of non-protein-coding RNA, including natural antisense RNA or pseudo genes, are largely unknown, it is thought that non-protein-coding RNA has a broad range of functions including roles in gene silencing, epigenetic control and ribozymes in eukaryotes (Amaral et al., 2008). Recent studies showed that several non-protein-coding RNAs participate in stress responses and organ development in plants (Dai et al., 2007; Franco-Zorrilla et al., 2007; Ben Amor et al., 2009). It appears that identification of conserved or unique non-protein-coding RNA is one way to find functional non-protein-coding RNA in Arabidopsis seeds (Rymarquis et al., 2008).
Conclusions and future perspectives
In this study, we have demonstrated that the effects of exogenous ABA on ABA-mediated transcription at early stages of seed imbibition differ from those of endogenous ABA. The effects of exogenous ABA were prominent in the expression of several ABA-related genes at a later stage of imbibition. We performed large-scale expression studies on Arabidopsis seeds using tiling arrays. A large number of stored mRNA species in dry seeds were not regulated by endogenous ABA levels, suggesting that these stored mRNAs might not influence seed dormancy and germination. After seed imbibition, endogenous ABA affected the expression of critical components, e.g. ABA signaling, photosynthesis, physiological and metabolic genes including a GA biosynthesis enzyme. Some of these genes were differentially regulated in the different seed tissues, suggesting that they determine whether seeds remain dormant or germinate after imbibition. In addition, our tiling array analysis identified a large number of non-AGI TUs including non-protein-coding RNA. Numerous non-protein-coding RNAs were defined as antisense transcripts, and sense/antisense pairs showed similar expression patterns in dry and imbibed seeds. Like AGI code genes, ABA-responsive and tissue-specific non-AGI TUs were regulated in imbibed seeds. Here, we show that dynamic and complex transcriptional regulation occurs in seeds. Our large-scale data set will contribute to future TAIR gene models and will increase our understanding of the molecular basis of how endogenous ABA controls seed dormancy and germination.
Plant materials and growth conditions
In this study, both the wild type and mutants were A. thaliana accession Columbia. The aba2-1 mutant was isolated previously (LeonKloosterziel et al., 1996). The cyp707a1a2a3 triple mutant was isolated by crossing the cyp707a1-1 cyp707a2-1 double mutant and the cyp707a2-1 cyp707a3-1 double mutant (Okamoto et al., 2006). Plants were grown in a growth chamber at 22°C and 50–60% relative humidity under a 16-h light/8-h dark cycle. Seeds were harvested from yellow-brown siliques and were immediately used in this study. For germination tests, freshly harvested seeds were sown on a 0.5% agarose gel (LO3; TAKARA, http://www.takara-bio.com/) and the plates were kept at 22°C under continuous light conditions. To obtain seed samples for ABA measurement and RNA extraction, 30–60 mg seeds were imbibed in 8.5 cm Petri dishes containing two layers of filter paper (approximately 7 cm diameter) and 2 ml water and harvested. Dissection of embryo and testa/endosperm from 24-h imbibed seeds was carried out under a stereoscopic microscope.
Extraction, purification and quantification of ABA were carried out as described in Saika et al. (2007).
For RT-PCR and tiling array analyses, total RNA was isolated as described in Kushiro et al. (2004). For northern blot analysis and RNA isolation from the dissected embryo and endosperm tissues, extraction was carried out as described previously (Martin et al., 2005).
First-strand cDNA synthesis and quantitative RT-PCR (qRT-PCR) using SYBR Green I were performed as described previously (Okamoto et al., 2006). Sequences of primers used for RT-PCR are shown in Table S14.
Arabidopsis genome sequence and annotation information from TAIR 8 was mapped to the probes of the Affymetrix Arabidopsis whole-genome tiling array. The tiling array data analysis was carried out essentially as described previously (Matsui et al., 2008). The expressed AGI code genes and non-AGI TUs were detected using the ARTADE program (P initial value <10−8) (Toyoda and Shinozaki, 2005). To detect non-protein-coding RNAs, we carried out homology searches of non-AGI TUs against registered protein sequence data sets (NIH NR database) using the BLASTX program (Matsui et al., 2008). Comparisons of non-AGI TUs with cDNAs and MPSS tags and identification of sense/antisense transcript pairs were also carried out as described previously (Matsui et al., 2008). In analysis of evolutionary conservation of non-AGI TUs in intergenic regions, homology searches of the non-AGI TU against the EST sequences of 10 plant species (NCBI Unigene database, http://www.ncbi.nlm.nih.gov/sites/entrez?db=unigene) was carried out using the BLASTN program (E value <10−10). To conduct hierarchical clustering analysis for the AGI code genes and non-AGI TUs, tiling array data (signal intensity, physical position and P initial value) were entered into GENESPRING 7.3. In the PCA, 15 331 genes that were significantly differentially expressed in at least one condition (FDR <0.05, P initial value <10−8) were subjected to Z-scaling using genefilter, prcomp, princomp and the R statistical analysis packages (Ihaka and Gentleman, 1996). Genes were ranked in order of their PC1 and PC2 scores (Table S2). To identify ABA-responsive and differentially regulated AGI code genes and non-AGI TUs among samples, significant differences were judged by the Mann–Whitney U-test (FDR α = 0.05) using the all probes (5.8 million perfect match and 5.8 million mismatch probes) as described previously (Storey, 2002; Storey and Tibshirani, 2003; Matsui et al., 2008). Regulatory cis elements for differentially regulated AGI code genes and non-AGI code TUs were identified using genespring 7.3 software. Developmental signatures associated with differentially regulated genes were defined using the TAGGIT workflow list (Carrera et al., 2007). Arabidopsis tiling array data used in this study is available at GEO (http://www.ncbi.nlm.nih.gov/geo/info/linking.html) under the accession number GSE15700.
Northern analysis was performed using a DIG Northern Starter Kit (Roche Applied Science, http://www.roche-applied-science.com/). Complementary DNA fragments for non-AGI TUs and AGI code genes were subcloned into pSTBlue-1 vector (Novagen, http://www.merck.de/en/index.html) and were amplified by PCR using forward and reverse M13 primers. Sequences of cDNA fragments for non-AGI TUs and AGI code genes are shown in Table S14. The PCR products were used as templates for synthesis of digoxigenin (DIG)-labeled antisense RNA probes with T7 or SP6 RNA polymerase. Total RNA (40 μg) was separated by electrophoresis on a 1.2% agarose gel containing 2.2 m formaldehyde. After gel blotting, the membranes (Hybond N; Amersham Biosciences, http://www.gelifesciences.co.jp) were hybridized with the RNA probe using DIG Easy Hyb Granules (Roche Applied Science). The membranes were washed using the DIG Wash and Block Buffer Set (Roche Applied Science). The hybridized probes were immunologically detected with anti-DIG-AP and visualized with the chemiluminescence substrate CDP-Star (Roche Applied Science). Chemiluminescence was detected using Hyperfilm ECL (Amersham Biosciences).
We thank Dr Ian Graham for providing microarray data, Ms Sachiyo Harada for technical assistance and the Arabidopsis Biological Resource Center (ABRC) for providing T-DNA-tagged lines. This work was supported by the Special Postdoctoral Researcher’s Program from RIKEN (to MO) and a grant from RIKEN Plant Science Center (to MS).