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Real Time based RT-PCR Detection of DUF538 Gene Expression in Drought-Challenged Celosia

机译:实时RT-PCR检测干旱挑战鸡冠花中DUF538基因的表达

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To enhance our information in plant system of DUF538 (domain of unknown function 538) protein superfamily, our efforts were made to unravel the relative expression patterns of Celosia DUF538 transcript using real time reverse transcription and polymerase chain reaction (RT-PCR) with template materials collected from the leaves of test plant grown under drought stress condition. The results indicated that DUF538 transcript is highly detectable in drought-challenged leaf tissues. In comparison with non-stressed tissues, the expression level of DUF538 gene was detected about 3.2 - 3.6 folds increase in stressed leaves. The results suggested that DUF538 gene activity may be as one of the drought stress defense responses (possibly though the hydrolytic mechanism) in plant system.
机译:为了增强我们在DUF538(功能未知的域538)蛋白超家族植物系统中的信息,我们通过实时逆转录和聚合酶链反应(RT-PCR)与模板材料一起研究了鸡冠花DUF538转录本的相对表达模式。从在干旱胁迫条件下生长的测试植物的叶片中收集。结果表明,DUF538转录本在干旱挑战的叶片组织中高度可检测。与未胁迫的组织相比,在胁迫的叶片中检测到DUF538基因的表达水平增加了约3.2-3.6倍。结果表明,DUF538基因活性可能是植物系统中干旱胁迫防御反应之一(可能是通过水解机制)。

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