首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Quantification of XPA gene expression levels in human and mouse cell lines by competitive RT-PCR.
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Quantification of XPA gene expression levels in human and mouse cell lines by competitive RT-PCR.

机译:通过竞争性RT-PCR定量检测人和小鼠细胞系中XPA基因的表达水平。

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摘要

Expression of the mammalian photoproduct-specific DNA-binding protein XPA has been quantified by competitive reverse transcription-polymerase chain reaction, a method that provides relative numbers of mRNA molecules per cell. Human primary and simian virus (SV)40-transformed fibroblasts had 4.8 and 8.4 transcripts per cell, respectively; mouse embryonic and SV40-transformed fibroblasts had 6.7 and 5.5 transcripts per cell, respectively. None of these differences are significant, and the mean value of 5 to 8 transcripts per cell indicates that XPA is expressed as a low-abundance mRNA. Two cell lines transfected with XPA on a conditional promoter showed different numbers of XPA mRNA molecules, consistent with their respective responses to an inducer and their sensitivity to ultraviolet light. The similarity of results in human and mouse cells shows that a difference in XPA expression cannot account for the greater repair of nontranscribed DNA in human cells.
机译:哺乳动物光产物特异性DNA结合蛋白XPA的表达已通过竞争性逆转录聚合酶链反应进行了定量,该方法可提供每个细胞相对数量的mRNA分子。人原代和猿猴病毒(SV)40转化的成纤维细胞每个细胞分别具有4.8和8.4的转录本。小鼠胚胎和SV40转化的成纤维细胞每个细胞分别有6.7和5.5个转录本。这些差异均不显着,每个细胞5至8个转录本的平均值表明XPA被表达为低丰度mRNA。在条件启动子上用XPA转染的两种细胞系显示出不同数量的XPA mRNA分子,这与它们对诱导物的各自反应和对紫外线的敏感性一致。人类和小鼠细胞中结果的相似性表明XPA表达的差异不能解释人类细胞中非转录DNA的更大修复。

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