首页> 外文期刊>Nucleic Acids Research >DNA REPAIR DEFICIENCIES ASSOCIATED WITH MUTATIONS IN GENES ENCODING SUBUNITS OF TRANSCRIPTION INITIATION FACTOR TFIIH IN YEAST
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DNA REPAIR DEFICIENCIES ASSOCIATED WITH MUTATIONS IN GENES ENCODING SUBUNITS OF TRANSCRIPTION INITIATION FACTOR TFIIH IN YEAST

机译:酵母中转录起始因子TFIIH亚基编码突变的DNA修复缺陷

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摘要

Several proteins, including Rad3 and Rad25(Ssl2), are essential for nucleotide excision repair (NER) and function in the RNA polymerase II transcription initiation complex TFIIH, Mutations in genes encoding two other subunits of TFIIH, TFB1 and SSL1, result in UV sensitivity and have been shown to take part in NER in an in vitro system, However, a deficiency in global NER does not exclude the possibility that such repair-deficient mutants can perform transcription-coupled repair (TCR), as shown for xeroderma pigmentosum group C, To date, temperature-sensitive C-terminal truncations of Tfb1 are the only TFIIH mutations that result in intermediate UV sensitivity, which might indicate a deficiency in either the global NER or TCR pathways. We have directly analyzed both TCR and global NER in these mutants, We found that ssl1, rad3 and tfb1 mutants, like rad25(ssl2-xp) mutants, are deficient in both the global NER and TCR pathways, Our results support the view that the mutations in any one of the genes encoding subunits of TFIIH result in deficiencies in both global and TCR pathways of NER, We suggest that when subunits of TFIIH are in limiting amounts, TCR may preclude global NER.
机译:几种蛋白质,包括Rad3和Rad25(Ssl2),对于核苷酸切除修复(NER)必不可少,并在RNA聚合酶II转录起始复合体TFIIH中起作用。编码TFIIH,TFB1和SSL1的其他两个亚基的基因突变会导致紫外线敏感性并且已经证明在体外系统中参与NER。但是,整体NER的缺乏并不排除这种缺乏修复的突变体可以进行转录偶联修复(TCR)的可能性,如针对干性色素C组迄今为止,Tfb1的温度敏感性C端截短是导致中等UV敏感性的唯一TFIIH突变,这可能表明总体NER或TCR途径均缺乏。我们直接分析了这些突变体中的TCR和全局NER。我们发现ssl1,rad3和tfb1突变体(如rad25(ssl2-xp)突变体)在全局NER和TCR途径中均缺乏,我们的结果支持以下观点:编码TFIIH亚基的任何一种基因的突变都会导致NER的整体和TCR途径均缺乏,我们建议当TFIIH的亚基含量有限时,TCR可能会排除整体NER。

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