高粱ATP合成酶E亚基基因(SbATPase-E)的克隆及其抗逆功能研究
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农业部转基因专项(2014ZX08003-004);国家自然科学基金项目(重点项目);中国农科院创新工程;河北省自然基金项目(C2012407002)


Isolation of ATP synthase subunit E gene in sorghum (SbATPase-E) and its functional analysis related to stress tolerance
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National Science and Technology Major Project (2014ZX08003-004);The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan); Innovation program of CAAS; Natural science foundation of Hebei Province

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    摘要:

    高粱是一种抗旱性较强的禾谷类作物。本研究在高粱中克隆到一个全长为693 bp的编码ATP合成酶E亚基的基因(SbATPase-E)。在高粱幼苗期,SbATPase-E基因受NaCl和脱落酸(ABA)处理诱导上调表达。该基因在拟南芥中过量表达可提高转基因植株的耐旱性和耐盐性,在逆境胁迫条件下转基因拟南芥植株较野生型植株根系发达,可能是转基因植株耐旱性和耐盐性提高的主要原因。在干旱胁迫条件下,转基因植株中DREB2A、P5CS1、RD29A、RAB18和ABI1基因的表达量相对于野生型植株中的表达量提高更为显著提高;在高盐处理条件下,转基因植株中SOS1、和SOS2和SOS3基因的表达量也较野生型植株中的表达量提高更为明显。这些抗逆相关基因的上调表达可能是转基因植株抗逆性提高的主要分子机制。

    Abstract:

    Sorghum (Sorghum bicolor) is a cereal crop with strong drought tolerance. In the presentthis study a gene encoding ATP synthase subunit E with 230 amino acids was cloned in sorghum, whose full length was 693 bp and named SbATPase-E. Under NaCl and ABA treatment, The SbATPase-E geneshowed an up-regulated expression a was induced by NaCl and ABA treatment in seedlingt the seedling stage. Heterologous Overover-expression of SbATPase-E could enhance drought and salt tolerance in Arabidopsis thaliana. Further study found that the improved drought and salt tolerance in the transgenic plants was associated with a more extensive larger root systems in transgenic lines compared with the wild type plants. Moreover, the expression levels of DREB2A, P5CS1, RD29A, RAB18 and ABI1 in the transgenic plants under drought conditions were higher than that in the wild type, and the expression transcript levels of SOS1, and SOS2 and SOS3 in the transgenic plants under high salt treatment were also higher. The up-regulation of these stress response genes may suggest the molecular mechanism of stress resistance in of SbATPase-E transgenic plants.

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张静,张登峰,孙永华,等.高粱ATP合成酶E亚基基因(SbATPase-E)的克隆及其抗逆功能研究[J].植物遗传资源学报,2016,17(5):897-905.

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  • 收稿日期:2015-11-30
  • 最后修改日期:2016-05-13
  • 录用日期:2016-05-23
  • 在线发布日期: 2016-09-07
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