Zhou Yi, Yang Ping, Cui Fenglei, Zhang Fantao, Luo Xiangdong, Xie Jiankun
College of Life Sciences, Jiangxi Normal University, Nanchang, China.
Institute for Advanced Study, Jiangxi Normal University, Nanchang, China.
PLoS One. 2016 Jan 11;11(1):e0146242. doi: 10.1371/journal.pone.0146242. eCollection 2016.
Dongxiang wild rice (Oryza rufipogon Griff.) is the progenitor of cultivated rice (Oryza sativa L.), and is well known for its superior level of tolerance against cold, drought and diseases. To date, however, little is known about the salt-tolerant character of Dongxiang wild rice. To elucidate the molecular genetic mechanisms of salt-stress tolerance in Dongxiang wild rice, the Illumina HiSeq 2000 platform was used to analyze the transcriptome profiles of the leaves and roots at the seedling stage under salt stress compared with those under normal conditions. The analysis results for the sequencing data showed that 6,867 transcripts were differentially expressed in the leaves (2,216 up-regulated and 4,651 down-regulated) and 4,988 transcripts in the roots (3,105 up-regulated and 1,883 down-regulated). Among these differentially expressed genes, the detection of many transcription factor genes demonstrated that multiple regulatory pathways were involved in salt stress tolerance. In addition, the differentially expressed genes were compared with the previous RNA-Seq analysis of salt-stress responses in cultivated rice Nipponbare, indicating the possible specific molecular mechanisms of salt-stress responses for Dongxiang wild rice. A large number of the salt-inducible genes identified in this study were co-localized onto fine-mapped salt-tolerance-related quantitative trait loci, providing candidates for gene cloning and elucidation of molecular mechanisms responsible for salt-stress tolerance in rice.
东乡野生稻(Oryza rufipogon Griff.)是栽培稻(Oryza sativa L.)的祖先,以其对寒冷、干旱和疾病的超强耐受性而闻名。然而,迄今为止,关于东乡野生稻的耐盐特性知之甚少。为了阐明东乡野生稻耐盐胁迫的分子遗传机制,利用Illumina HiSeq 2000平台分析了盐胁迫下与正常条件下相比,幼苗期叶片和根系的转录组图谱。测序数据的分析结果表明,叶片中有6867个转录本差异表达(2216个上调,4651个下调),根系中有4988个转录本差异表达(3105个上调,1883个下调)。在这些差异表达基因中,许多转录因子基因的检测表明,多个调控途径参与了盐胁迫耐受性。此外,将差异表达基因与之前对栽培稻日本晴盐胁迫反应的RNA-Seq分析进行比较,揭示了东乡野生稻盐胁迫反应可能的特定分子机制。本研究中鉴定出的大量盐诱导基因共定位于精细定位的耐盐相关数量性状位点上,为水稻耐盐胁迫基因克隆和分子机制阐明提供了候选基因。