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对在无碱基位点启动碱基切除修复的酶的表征。

Characterization of enzymes that initiate base excision repair at abasic sites.

作者信息

Deutsch Walter A, Hegde Vijay

机构信息

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, USA.

出版信息

Methods Mol Biol. 2006;314:355-64. doi: 10.1385/1-59259-973-7:355.

Abstract

Abasic sites in DNA arise under a variety of circumstances, including destabilization of bases through oxidative stress, as an intermediate in base excision repair, and through spontaneous loss. Their persistence can yield a blockade to RNA transcription and DNA synthesis and can be a source of mutations. Organisms have developed an enzymatic means of repairing abasic sites in DNA that generally involves a DNA repair pathway that is initiated by a repair protein creating a phosphodiester break ("nick") adjacent to the site of base loss. Here we describe a method for analyzing the manner in which repair endonucleases differ in the way they create nicks in DNA and how to distinguish between them using cellular crude extracts.

摘要

DNA中的无碱基位点可在多种情况下产生,包括碱基因氧化应激而不稳定、作为碱基切除修复的中间体以及自发丢失。它们的持续存在会阻碍RNA转录和DNA合成,并且可能是突变的来源。生物体已经开发出一种修复DNA中无碱基位点的酶促方法,该方法通常涉及一种DNA修复途径,该途径由一种修复蛋白启动,该蛋白在碱基丢失位点附近产生磷酸二酯键断裂(“切口”)。在这里,我们描述了一种分析修复核酸内切酶在DNA中产生切口的方式以及如何使用细胞粗提物区分它们的方法。

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