NARO Institute of Fruit Tree Science, Tsukuba, Ibaraki 305-8605 Japan.
Plant Cell Physiol. 2013 Jul;54(7):1132-51. doi: 10.1093/pcp/pct067. Epub 2013 Apr 26.
The transcriptomes of endodormant and ecodormant Japanese pear (Pyrus pyrifolia Nakai 'Kosui') flower buds were analyzed using RNA-seq technology and compared. Among de novo assembly of 114,191 unigenes, 76,995 unigenes were successfully annotated by BLAST searches against various databases. Gene Ontology (GO) enrichment analysis revealed that oxidoreductases were enriched in the molecular function category, a result consistent with previous observations of notable changes in hydrogen peroxide concentration during endodormancy release. In the GO categories related to biological process, the abundance of DNA methylation-related gene transcripts also significantly changed during endodormancy release, indicating the involvement of epigenetic regulation. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis also showed the changes in transcript abundance of genes involved in the metabolism of various phytohormones. Genes for both ABA and gibberellin biosynthesis were down-regulated, whereas the genes encoding their degradation enzymes were up-regulated during endodormancy release. In the ethylene pathway, 1-aminocyclopropane-1-carboxylate synthase (ACS), a gene encoding the rate-limiting enzyme for ethylene biosynthesis, was induced towards endodormancy release. All of these results indicated the involvement of phytohormones in endodormancy release. Furthermore, the expression of dormancy-associated MADS-box (DAM) genes was down-regulated concomitant with endodormancy release, although changes in the abundance of these gene transcripts were not as significant as those identified by transcriptome analysis. Consequently, characterization of the Japanese pear transcriptome during the transition from endormancy to ecodormancy will provide researchers with useful information for data mining and will facilitate further experiments on endodormancy especially in rosaceae fruit trees.
利用 RNA-seq 技术分析了休眠和生态休眠日本梨(Pyrus pyrifolia Nakai 'Kosui')花芽的转录组,并进行了比较。在 114191 条 unigenes 的从头组装中,通过对各种数据库的 BLAST 搜索,成功注释了 76995 条 unigenes。基因本体论(GO)富集分析显示,氧化还原酶在分子功能类别中富集,这与先前观察到的休眠解除过程中过氧化氢浓度显著变化的结果一致。在与生物过程相关的 GO 类别中,DNA 甲基化相关基因转录本的丰度在休眠解除过程中也发生了显著变化,表明存在表观遗传调控。京都基因与基因组百科全书(KEGG)通路分析也显示了参与各种植物激素代谢的基因转录丰度的变化。ABA 和赤霉素生物合成的基因下调,而其降解酶的基因上调。在乙烯途径中,1-氨基环丙烷-1-羧酸合酶(ACS),编码乙烯生物合成的限速酶的基因,在休眠解除过程中被诱导。所有这些结果表明植物激素参与了休眠解除。此外,休眠相关 MADS 盒(DAM)基因的表达随着休眠的解除而下调,尽管这些基因转录本丰度的变化不如转录组分析中鉴定的那么显著。因此,描述日本梨从休眠到生态休眠的转变过程中的转录组,将为研究人员提供数据挖掘的有用信息,并有助于进一步研究休眠,特别是蔷薇科果树的休眠。