DNA Break Mapping Reveals Topoisomerase II Activity Genome-Wide

被引:64
|
作者
Baranello, Laura [1 ]
Kouzine, Fedor [1 ]
Wojtowicz, Damian [2 ]
Cui, Kairong [3 ]
Przytycka, Teresa M. [2 ]
Zhao, Keji [3 ]
Levens, David [1 ]
机构
[1] NCI, Pathol Lab, NIH, Bethesda, MD 20892 USA
[2] NCBI, Computat Biol Branch, NLM, NIH, Bethesda, MD 20894 USA
[3] NHLBI, Syst Biol Ctr, NIH, Bethesda, MD 20892 USA
来源
基金
美国国家卫生研究院;
关键词
topoisomerases; DNA damage; transcription; DOUBLE-STRAND BREAK; CLEAVABLE COMPLEXES; TRANSCRIPTION; REPAIR; BETA; CHROMATIN; DISEASE; DAMAGE; ALPHA; CELLS;
D O I
10.3390/ijms150713111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genomic DNA is under constant assault by endogenous and exogenous DNA damaging agents. DNA breakage can represent a major threat to genome integrity but can also be necessary for genome function. Here we present approaches to map DNA double-strand breaks (DSBs) and single-strand breaks (SSBs) at the genome-wide scale by two methods called DSB- and SSB-Seq, respectively. We tested these methods in human colon cancer cells and validated the results using the Topoisomerase II (Top2)-poisoning agent etoposide (ETO). Our results show that the combination of ETO treatment with break-mapping techniques is a powerful method to elaborate the pattern of Top2 enzymatic activity across the genome.
引用
收藏
页码:13111 / 13122
页数:12
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