桑树(Morus L.)蛋氨酸亚砜还原酶基因的克隆、序列分析及其在植物发育和胁迫响应中的表达。

Bioorganicheskaia khimiia Pub Date : 2013-09-01
Wei Tong, Yinghua Zhang, Heng Wang, Feng Li, Zhaoyue Liu, Yuhua Wang, Rongjun Fang, Weiguo Zhao, Long Li
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引用次数: 0

摘要

蛋氨酸亚砜还原酶在植物生长发育中起调节作用,特别是通过恢复蛋白质中蛋氨酸的氧化来清除活性氧。利用桑树表达序列标签(ESTs)克隆了桑树甲硫氨酸亚砜还原酶(methionine亚砜reductase, MSR)全长cDNA序列,并将其命名为MMSR。序列分析表明,MMSR全长810 bp,编码194个氨基酸,预测分子量为21.6 kDa,等电点为6.78。采用qRT-PCR方法测定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,胁迫条件下的表达量发生了显著变化。这有助于我们更好地了解桑树胁迫反应的信号转导机制的分子基础。
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Mulberry (Morus L.) methionine sulfoxide rreductase gene cloning, sequence analysis, and expression in plant development and stress response.

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 full-length 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.

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