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酵母RAD7和RAD16基因是核苷酸切除修复过程中切口后事件所必需的。对rad7和rad16突变体进行的体外和体内研究以及对含Rad7/Rad16蛋白复合物的纯化。

The yeast RAD7 and RAD16 genes are required for postincision events during nucleotide excision repair. In vitro and in vivo studies with rad7 and rad16 mutants and purification of a Rad7/Rad16-containing protein complex.

作者信息

Reed S H, You Z, Friedberg E C

机构信息

Laboratory of Molecular Pathology, Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas 75235-9072, USA.

出版信息

J Biol Chem. 1998 Nov 6;273(45):29481-8. doi: 10.1074/jbc.273.45.29481.

Abstract

In eukaryotes, nucleotide excision repair (NER) is a complex reaction requiring multiple proteins. In the yeast Saccharomyces cerevisiae, two of these proteins, Rad7 and Rad16, are specifically involved in the removal of lesions from transcriptionally silent regions of the genome in vivo. Extracts prepared from rad7 or rad16 mutant cells are deficient, but not totally defective, in both oligonucleotide excision and repair synthesis of damaged plasmid DNA. We show that these extracts are, however, fully proficient in the incision step of the NER reaction in vitro. Furthermore, using a cdc9 mutant to trap incision intermediates, we demonstrate that rad7 and rad16 mutants are proficient in NER-dependent DNA incision in vivo. A purified protein complex containing both Rad7 and Rad16 proteins complements the oligonucleotide excision and repair synthesis defects in rad7 and rad16 mutant extracts. We conclude that the products of the RAD7 and RAD16 genes are involved in a postincision event(s) during NER in yeast.

摘要

在真核生物中,核苷酸切除修复(NER)是一个需要多种蛋白质参与的复杂反应。在酿酒酵母中,其中两种蛋白质Rad7和Rad16,在体内特异性地参与从基因组转录沉默区域去除损伤。从rad7或rad16突变细胞制备的提取物在受损质粒DNA的寡核苷酸切除和修复合成方面存在缺陷,但并非完全有缺陷。然而,我们发现这些提取物在体外NER反应的切口步骤中完全具备能力。此外,使用cdc9突变体捕获切口中间体,我们证明rad7和rad16突变体在体内NER依赖性DNA切口方面具备能力。一种同时含有Rad7和Rad16蛋白的纯化蛋白复合物弥补了rad7和rad16突变提取物中的寡核苷酸切除和修复合成缺陷。我们得出结论,RAD7和RAD16基因的产物参与酵母NER过程中的切口后事件。

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