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首页> 外文期刊>Russian journal of bioorganic chemistry >Mulberry (Morus L.) methionine sulfoxide reductase gene cloning, sequence analysis, and expression in plant development and stress response
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Mulberry (Morus L.) methionine sulfoxide reductase gene cloning, sequence analysis, and expression in plant development and stress response

机译:桑(甲桑)蛋氨酸亚砜还原酶基因的克隆,序列分析及在植物发育和胁迫响应中的表达

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Methionine sulfoxide reductase plays a regulatory role in plant growth and development, especially in scavenging reactive oxygen species by restoration of the oxidation of methionine in protein. A fulllength cDNA sequence encoding methionine sulfoxide reductase (MSR) from mulberry, which we designated MMSR, was cloned based on mulberry expressed sequence tags (ESTs). Sequence analysis showed that the MMSR is 810 bp long, encoding 194 amino acids with a predicted molecular weight of 21.6 kDa and an isoelectric point of 6.78. The expression level of the MMSR gene under conditions of drought and salt stresses was quantified by qRT-PCR. The results show that the expression level changed significantly under the stress conditions compared to the normal growth environment. It helps us to get a better understanding of the molecular basis for signal transduction mechanisms underlying the stress response in mulberry.
机译:蛋氨酸亚砜还原酶在植物生长和发育中起调节作用,特别是通过恢复蛋白质中蛋氨酸的氧化来清除活性氧。基于桑树表达的序列标签(EST),克隆了来自桑树的蛋氨酸亚砜还原酶(MSR)的全长cDNA序列,我们将其命名为MMSR。序列分析表明,MMSR长810 bp,编码194个氨基酸,预测分子量为21.6 kDa,等电点为6.78。通过qRT-PCR定量分析在干旱和盐胁迫条件下MMSR基因的表达水平。结果表明,与正常生长环境相比,在胁迫条件下表达水平发生了显着变化。它有助于我们更好地理解桑树应激反应背后的信号转导机制的分子基础。

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