Drosophila melanogaster RECQ5/QE DNA helicase:: stimulation by GTP binding

被引:45
作者
Kawasaki, K
Maruyama, S
Nakayama, M
Matsumoto, K
Shibata, T
机构
[1] RIKEN, Inst Phys & Chem Res, Mol Cell Biol Lab, Wako, Saitama 3510198, Japan
[2] RIKEN, Inst Phys & Chem Res, Bioarchitect Res Grp, Wako, Saitama 3510198, Japan
[3] JST, CREST, Wako, Saitama 3510198, Japan
[4] Saitama Univ, Fac Biosci & Biotechnol, Dept Biol Mol, Saitamashi, Saitama 3388570, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1093/nar/gkf487
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
The Drosophila melanogaster RECQ5/QE gene encodes a member of the DNA helicase family comprising the Escherichia coli RecQ protein and products of the human Bloom's, Werner's, and Rothmund-Thomson syndrome genes. The full-length product of RECQ5/QE was expressed in the baculovirus system and was purified. Gel filtration experiments indicated that RECQ5/QE was present in an oligomeric state. The RECQ5/QE protein hydrolyzed ATP and even more actively GTP in the presence of single-stranded DNA. ATP drove the DNA helicase activity of RECQ5/QE, whereas GTP had little effect. GTP exhibited a stimulatory effect on DNA unwinding when it was used together with ATP. This effect was more apparent with non-hydrolyzable GTP analogs, such as GTPgammaS and GMPPNP. These results indicate that GTP binding to RECQ5/QE triggers its DNA helicase activity. GTP binding increased the rate of strand separation without affecting the S-0.5 (K-m) values for the substrates during the DNA helicase reaction. The data collectively suggest that the RECQ5/QE protein is activated upon GTP binding through the ATP-binding site.
引用
收藏
页码:3682 / 3691
页数:10
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