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Arabidopsis Root-Abundant Cytosolic Methionine Sulfoxide Reductase B Genes MsrB7 and MsrB8 are Involved in Tolerance to Oxidative Stress

机译:拟南芥根丰富的胞质蛋氨酸亚砜还原酶B基因MsrB7和MsrB8参与对氧化应激的耐受性。

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摘要

Excess reactive oxygen species (ROS) accumulation under various environmental stresses can damage intracellular polysaccharides, DNA, lipids and proteins. Methionine sulfoxide reductase (MSR) participates in a protein repair system that is one of the defensive mechanisms that diminishes oxidative destruction. In Arabidopsis, cytosolic MsrB7 and MsrB8 are oxidative stress-inducible protein repair enzymes that are abundant in the root. Here methyl viologen (MV) treatment was demonstrated to increase greatly the accumulation of H2O2 in MsrB7-knockdown, MsrB8-knockdown and wild-type Arabidopsis, but not in transgenic plants overexpressing MsrB7 or MsrB8. The reduction in H2O2 level under MV treatment in these overexpressing plants coincided with increased activity of glutathione S-transferase (GST), a herbicide-detoxifying enzyme. MsrB7 and MsrB8 are suggested to play an important role in defense against oxidative stress. Transgenic plants overexpressing MsrB7 or MsrB8 were viable and survived after MV and H2O2 treatment. Ectopic expression of specific cytosolic MsrB genes may be useful for application in crop improvement.
机译:在各种环境压力下过量的活性氧(ROS)积累会破坏细胞内多糖,DNA,脂质和蛋白质。蛋氨酸亚砜还原酶(MSR)参与蛋白质修复系统,该系统是减少氧化破坏的防御机制之一。在拟南芥中,胞质MsrB7和MsrB8是氧化应激诱导的蛋白质修复酶,在根中含量丰富。此处证明了甲基紫精(MV)处理可大大增加Hssub2击倒,MsrB8击倒和野生型拟南芥中H 2 O 2 的积累,而在过表达MsrB7或MsrB8的转基因植物。在这些过表达植物中,MV处理下H 2 O 2 水平的降低与除草剂解毒酶谷胱甘肽S-转移酶(GST)的活性增加有关。建议MsrB7和MsrB8在防御氧化应激中起重要作用。 MV和H 2 O 2 处理后,过表达MsrB7或MsrB8的转基因植物存活并存活。特异的胞质MsrB基因的异位表达可用于作物改良。

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  • 来源
    《Plant and Cell Physiology》 |2012年第10期|p.1707-1719|共13页
  • 作者单位

    1Academia Sinica Biotechnology Center in Southern Taiwan, Tainan 741, Taiwan 2Agricultural Biotechnology Research Center, Academia Sinica, Taipei, 115, Taiwan 3Institute of Biotechnology, National Cheng Kung University, Tainan, 701, Taiwan 4Molecular and Biological Agricultural Sciences Program, Taiwan International Graduate Program, Academia Sinica, Taipei 115, Taiwan 5Graduate Institute of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan 6Department of Life Science, National Taiwan Normal University, Taipei 116, Taiwan 7These authors contributed equally to this work.;

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