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大肠杆菌和人类核苷酸切除修复酶系统的纯化与特性分析。

Purification and characterization of Escherichia coli and human nucleotide excision repair enzyme systems.

作者信息

Reardon Joyce T, Sancar Aziz

机构信息

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

出版信息

Methods Enzymol. 2006;408:189-213. doi: 10.1016/S0076-6879(06)08012-8.

Abstract

Nucleotide excision repair is a multicomponent, multistep enzymatic system that removes a wide spectrum of DNA damage by dual incisions in the damaged strand on both sides of the lesion. The basic steps are damage recognition, dual incisions, resynthesis to replace the excised DNA, and ligation. Each step has been studied in vitro using cell extracts or highly purified repair factors and radiolabeled DNA of known sequence with DNA damage at a defined site. This chapter describes procedures for preparation of DNA substrates designed for analysis of damage recognition, either the 5' or the 3' incision event, excision (resulting from concerted dual incisions), and repair synthesis. Excision in Escherichia coli is accomplished by the three-subunit Uvr(A)BC excision nuclease and in humans by six repair factors: XPA, RPA, XPChR23B, TFIIH, XPFERCC1, and XPG. This chapter outlines methods for expression and purification of these essential repair factors and provides protocols for performing each of the in vitro repair assays with either the E. coli or the human excision nuclease.

摘要

核苷酸切除修复是一个多组分、多步骤的酶系统,它通过在损伤两侧的损伤链上进行双切口来去除多种DNA损伤。基本步骤包括损伤识别、双切口、重新合成以取代切除的DNA以及连接。每个步骤都已在体外使用细胞提取物或高度纯化的修复因子以及已知序列的放射性标记DNA进行研究,这些DNA在特定位点存在DNA损伤。本章描述了用于分析损伤识别、5'或3'切口事件、切除(由协同双切口产生)和修复合成的DNA底物的制备程序。大肠杆菌中的切除由三聚体Uvr(A)BC切除核酸酶完成,而人类中的切除由六个修复因子完成:XPA、RPA、XPChR23B、TFIIH、XPFERCC1和XPG。本章概述了这些必需修复因子的表达和纯化方法,并提供了使用大肠杆菌或人类切除核酸酶进行每种体外修复测定的方案。

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