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PMID: 11834724 已发表 · ppublish 英语

Homologous pairing and ring and filament structure formation activities of the human Xrcc2*Rad51D complex.

The Journal of biological chemistry ·第 277 卷 ·第 16 期 ·2002-06-07

Kurumizaka Hitoshi, Ikawa Shukuko, Nakada Maki, Enomoto Rima, Kagawa Wataru, Kinebuchi Takashi, Yamazoe Mitsuyoshi, Yokoyama Shigeyuki, Shibata Takehiko

摘要

The Xrcc2 and Rad51D/Rad51L3 proteins, which belong to the Rad51 paralogs, are required for homologous recombinational repair (HRR) in vertebrates. The Xrcc2 and Rad51D/Rad51L3 genes, whose products interact with each other, have essential roles in ensuring normal embryonic development. In the present study, we coexpressed the human Xrcc2 and Rad51D/Rad51L3 proteins (Xrcc2 and Rad51D, respectively) in Escherichia coli, and purified the Xrcc2*Rad51D complex to homogeneity. The Xrcc2 small middle dotRad51D complex catalyzed homologous pairing between single-stranded and double-stranded DNA, similar to the function of the Xrcc3*Rad51C complex, which is another complex of the Rad51 paralogs. An electron microscopic analysis showed that Xrcc2*Rad51D formed a multimeric ring structure in the absence of DNA. In the presence of ssDNA, Xrcc2*Rad51D formed a filamentous structure, which is commonly observed among the human homologous pairing proteins, Rad51, Rad52, and Xrcc3*Rad51C.

文献信息
期刊
The Journal of biological chemistry
期刊简称
J Biol Chem
发表日期
2002-06-07
收录日期
2002-04-15
更新日期
2013-11-21
语言
英语
国家/地区
United States
NLM ID
2985121R
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