Jin Xiaofang, Liu Dandan, Ma Linlong, Gong Ziming, Cao Dan, Liu Yanli, Li Yeyun, Jiang Changjun
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, Hefei, Anhui 230036, China.
Fruit and Tea Research Institute, Hubei Academy of Agricultural Sciences, Wuhan, Hubei 430064, China.
Int J Genomics. 2018 Jun 5;2018:5963797. doi: 10.1155/2018/5963797. eCollection 2018.
The tea plant ( (L.) O. Kuntze) is an economically important woody perennial nonalcoholic health beverage crop. Tea seeds are categorized as recalcitrant and are sensitive to dehydration treatment. However, the molecular basis of this phenomenon has not been investigated. Thus, we analyzed the genome-wide expression profiles of three dehydration stages using RNA-Seq and digital gene expression (DGE) technologies. We performed de novo assembly and obtained a total of 91,925 nonredundant unigenes, of which 58,472 were extensively annotated. By a hierarchical clustering of differentially expressed genes (DEGs), we found that 8929 DEGs were downregulated and 5875 DEGs were upregulated during dehydration treatment. A series of genes related to ABA biosynthesis and signal transduction, transcription factor, antioxidant enzyme, LEA protein, and proline metabolism that have been reported to function in dehydration process were found to be downregulated. Additionally, the expression profiles of 12 selected genes related to tea seed dehydration treatment were confirmed by qRT-PCR analysis. To our knowledge, this is the first genome-wide study elucidating the possible molecular mechanisms of sensitivity of recalcitrant tea seeds to dehydration. The results obtained in this study contribute to the preservation of tea seeds as genetic resources and can also be used to explore the mechanism of dehydration sensitivity of other recalcitrant seeds.
茶树((L.) O. Kuntze)是一种具有重要经济价值的多年生木本非酒精健康饮料作物。茶籽属于顽拗型种子,对脱水处理敏感。然而,这一现象的分子基础尚未得到研究。因此,我们利用RNA测序(RNA-Seq)和数字基因表达(DGE)技术分析了三个脱水阶段的全基因组表达谱。我们进行了从头组装,共获得91,925个非冗余单基因,其中58,472个得到了广泛注释。通过对差异表达基因(DEG)进行层次聚类,我们发现脱水处理过程中有8929个DEG下调,5875个DEG上调。一系列与脱落酸(ABA)生物合成和信号转导、转录因子、抗氧化酶、胚胎发育晚期丰富蛋白(LEA)和脯氨酸代谢相关的基因,据报道在脱水过程中发挥作用,但被发现下调。此外,通过定量逆转录聚合酶链反应(qRT-PCR)分析证实了12个与茶籽脱水处理相关的选定基因的表达谱。据我们所知,这是第一项全基因组研究,阐明了顽拗型茶籽对脱水敏感的可能分子机制。本研究获得的结果有助于将茶籽作为遗传资源进行保存,也可用于探索其他顽拗型种子脱水敏感性的机制。