Deutsch Walter A, Hegde Vijay
Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, USA.
Methods Mol Biol. 2006;314:355-64. doi: 10.1385/1-59259-973-7:355.
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.
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。