Quantifying clustered DNA damage induction and repair by gel electrophoresis, electronic imaging and number average length analysis

被引:69
作者
Sutherland, BM
Georgakilas, AG
Bennett, PV
Laval, J
Sutherland, JC
机构
[1] Inst Gustave Roussy, LBPA ENS Cachan, CNRS, UMR 8113, F-94805 Villejuif, France
[2] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
[3] E Carolina Univ, Dept Phys, Greenville, NC 27858 USA
关键词
DOUBLE-STRAND BREAKS; BROMIDE-STAINED DNA; ESCHERICHIA-COLI; IONIZING-RADIATION; RESTRICTION FRAGMENTS; MOLECULAR LENGTH; OXIDATIVE DAMAGE; HUMAN-LEUKOCYTES; IRRADIATED DNA; HUMAN-CELLS;
D O I
10.1016/j.mrfmmm.2003.08.005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Assessing DNA damage induction, repair and consequences of such damages requires measurement of specific DNA lesions by methods that are independent of biological responses to such lesions. Lesions affecting one DNA strand (altered bases, abasic sites, single strand breaks (SSB)) as well as damages affecting both strands (clustered damages, double strand breaks) can be quantified by direct measurement of DNA using gel electrophoresis, gel imaging and number average length analysis. Damage frequencies as low as a few sites per gigabase pair (10(9) bp) can be quantified by this approach in about 50 ng of non-radioactive DNA, and single molecule methods may allow such measurements in DNA from single cells. This review presents the theoretical basis, biochemical requirements and practical aspects of this approach, and shows examples of their applications in identification and quantitation of complex clustered damages. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:93 / 107
页数:15
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