A nonradioactive restriction enzyme-mediated assay to detect DNA repair by Fe(II)/2-oxoglutarate-dependent dioxygenase

被引:7
作者
Shivange, Gururaj [1 ]
Kodipelli, Naveena [1 ]
Anindya, Roy [1 ]
机构
[1] Indian Inst Technol, Dept Biotechnol, Ordnance Factory Estate, Hyderabad 502205, Andhra Pradesh, India
关键词
Fe(II)/2-oxoglutarate-dependent dioxygenase; AlkB; Methyl methanesulfonate; DNA repair; ESCHERICHIA-COLI; OXIDATIVE DEMETHYLATION; DEOXYRIBONUCLEIC-ACID; ALKB; DAMAGE; LESIONS; AGENTS; RNA;
D O I
10.1016/j.ab.2014.07.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Escherichia coli DNA repair enzyme AlkB belongs to the Fe(II)/2-oxoglutarate-dependent dioxygenase family. It removes methyl groups from 1-methyl adenine (1-meA) and 3-methyl cytosine (3-meC) lesions present in single-stranded DNA by oxidative decarboxylation. In the current article, we describe an in vitro assay that permits rapid detection of AlkB activity. To achieve this, we generated methylated oligonucleotide using methyl methanesulfonate and then monitored DNA repair using a methylation-sensitive restriction enzyme and novel agarose gel electrophoresis system capable of resolving small oligonucleotides. Our approach overcomes several drawbacks of NAD(+)-dependent formaldehyde dehydrogenase-coupled assay and radioisotope-based assay for determining AlkB DNA repair activity. (c) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 37
页数:3
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