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核苷酸切除修复

Nucleotide excision repair.

作者信息

Sancar A, Tang M S

机构信息

Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill 27599.

出版信息

Photochem Photobiol. 1993 May;57(5):905-21. doi: 10.1111/j.1751-1097.1993.tb09233.x.

Abstract

Nucleotide excision repair is the major DNA repair mechanism in all species tested. This repair system is the sole mechanism for removing bulky adducts from DNA, but it repairs essentially all DNA lesions, and thus, in addition to its main function, it plays a back-up role for other repair systems. In both pro- and eukaryotes nucleotide excision is accomplished by a multisubunit ATP-dependent nuclease. The excision nuclease of prokaryotes incises the eighth phosphodiester bond 5' and the fourth or fifth phosphodiester bond 3' to the modified nucleotide and thus excises a 12-13-mer. The excision nuclease of eukaryotes incises the 22nd, 23rd, or 24th phosphodiester bond 5' and the fifth phosphodiester bond 3' to the lesion and thus removes the adduct in a 27-29-mer. A transcription repair coupling factor encoded by the mfd gene in Escherichia coli and the ERCC6 gene in humans directs the excision nuclease to RNA polymerase stalled at a lesion in the transcribed strand and thus ensures preferential repair of this strand compared to the nontranscribed strand.

摘要

核苷酸切除修复是所有已测试物种中的主要DNA修复机制。该修复系统是从DNA中去除大分子加合物的唯一机制,但它能修复基本上所有的DNA损伤,因此,除了其主要功能外,它还为其他修复系统发挥备份作用。在原核生物和真核生物中,核苷酸切除都是由多亚基ATP依赖性核酸酶完成的。原核生物的切除核酸酶在修饰核苷酸的5'端切割第八个磷酸二酯键,在3'端切割第四个或第五个磷酸二酯键,从而切除一个12 - 13聚体。真核生物的切除核酸酶在损伤位点的5'端切割第22、23或24个磷酸二酯键,在3'端切割第五个磷酸二酯键,从而以27 - 29聚体的形式去除加合物。大肠杆菌中由mfd基因和人类中由ERCC6基因编码的转录修复偶联因子将切除核酸酶导向停滞在转录链损伤处的RNA聚合酶,从而确保与非转录链相比,该链得到优先修复。

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