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Identification of a Putative Causal Gene of Salinity Tolerance in Soybean.

机译:大豆耐盐性的推定原因基因的鉴定。

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摘要

Whole genome sequencing data was used to assist genetic studies of wild soybean in our laboratory. Previously 31 soybean germplasms were re-sequenced. Recently, the de novo sequencing of a wild soybean genome (W05) and also re-sequencing of a core panel of 96 recombinant inbred lines originated from a salt tolerant wild soybean (W05) and a salt sensitive cultivated soybean (C08) were completed. Using this information, a major salt tolerance locus spanning 978 Kb in the soybean genome was identified through QTL study of the RI population.;In my research, this salt tolerance locus was further narrowed down to 388 Kb through extreme groups analysis. The observation that W05 accumulated less Na+ in leaves than C08 prompted me to focus on genes within this locus that are related to ion transportation . Making use of the de novo assembled scaffolds of W05 that cover the salt tolerance locus, a gene encoding an ion transporter (GmCHX1) was detected in W05 and the corresponding gene in C08 was found to be disrupted by a retrotransposon. 3'RACE and real-time PCR suggested that C08 produced a putatively loss-of-function truncated variant of GmCHX1. The coding sequence of GmCHX1 was conserved in salt tolerant soybean germplasms, but not in the salt sensitive germplasms. Moreover, the expression of GmCHX1 was found to be higher in the salt tolerant germplasms than in the sensitive germplasms. Ectopic expression of GmCHX1 from W05 can alleviate salt stress as well as reduce Na+ accumulation in transgenic models. Together, the results strongly support that GmCHX1 as a major determinant of salt tolerance in the wild soybean W05.
机译:全基因组测序数据被用于协助我们实验室中野生大豆的遗传研究。先前对31个大豆种质进行了重新测序。最近,野生大豆基因组(W05)的从头测序以及源自耐盐野生大豆(W05)和盐敏感栽培大豆(C08)的96个重组自交系核心序列的重测序完成。利用这些信息,通过RI群体的QTL研究确定了大豆基因组中跨978 Kb的主要耐盐基因座。在我的研究中,通过极端群体分析进一步将该耐盐基因座缩小到388 Kb。 W05在叶片中积累的Na +比C08少,这一发现促使我集中精力研究了该基因座中与离子转运有关的基因。利用覆盖盐耐性位点的W05的从头组装支架,在W05中检测到编码离子转运蛋白(GmCHX1)的基因,并且发现C08中的相应基因被反转录转座子破坏。 3'RACE和实时PCR提示C08产生了一个推测的功能丧失的GmCHX1截短变体。 GmCHX1的编码序列在耐盐大豆种质中保守,但在盐敏感性种质中不保守。此外,发现GmCHX1在耐盐种质中的表达高于敏感种质。来自W05的GmCHX1的异位表达可以缓解盐胁迫并减少转基因模型中的Na +积累。在一起的结果强烈支持GmCHX1是野生大豆W05中耐盐性的主要决定因素。

著录项

  • 作者

    Li, Man Wah.;

  • 作者单位

    The Chinese University of Hong Kong (Hong Kong).;

  • 授予单位 The Chinese University of Hong Kong (Hong Kong).;
  • 学科 Botany.;Genetics.;Molecular biology.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 141 p.
  • 总页数 141
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:53:34

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