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Activation of DNA cleavage by dynemicin A in a B-Z conformational junction.

作者信息

Ichikawa A, Kuboya T, Aoyama T, Sugiura Y

机构信息

Institute for Chemical Research, Kyoto University, Japan.

出版信息

Biochemistry. 1992 Jul 28;31(29):6784-7. doi: 10.1021/bi00144a019.

DOI:10.1021/bi00144a019
PMID:1379070
Abstract

We report here that the DNA strand scission by dynemicin A is not only sequence-specific but also conformation-specific. The salt-induced B----Z conformational transition dramatically enhanced the cleavage by dynemicin A in a B-Z junction region. By contrast, the bleomycin-Fe(II) complex, the elsamicin A-Fe(II) complex, and esperamicin A1 did not induce any preferential DNA cutting in such a DNA structure. The characteristic hyperreactivity of dynemicin A is observed in (dC-dG)8- and (dC-dG)12-inserted DNAs, but not in (dC-dG)5-inserted DNA. These results suggest value in the use of dynemicin A as proof of the existence of a B-Z junction in vivo and also may aid in understanding the structure of B-Z junctions.

摘要

相似文献

1
Activation of DNA cleavage by dynemicin A in a B-Z conformational junction.
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2
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Sequence preference for strand cleavage of gapped duplexes by dynemicin A: possible mechanism of sequence-dependent double-stranded breaks.强力霉素A对缺口双链体链切割的序列偏好性:序列依赖性双链断裂的可能机制
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引用本文的文献

1
The ultimate carcinogen of 4-nitroquinoline 1-oxide does not react with Z-DNA and hyperreacts with B-Z junctions.4-硝基喹啉1-氧化物的最终致癌物不与Z-DNA反应,而与B-Z连接区发生超反应。
Nucleic Acids Res. 1994 Feb 11;22(3):314-20. doi: 10.1093/nar/22.3.314.