A general model for site-specific recombination by the integrase family recombinases

被引:50
作者
Voziyanov, Y
Pathania, S
Jayaram, M [1 ]
机构
[1] Univ Texas, Dept Microbiol, Austin, TX 78712 USA
[2] Univ Texas, Inst Cell & Mol Biol, Austin, TX 78712 USA
[3] Inst Mol Biol & Genet, UA-252143 Kiev, Ukraine
基金
美国国家卫生研究院;
关键词
D O I
10.1093/nar/27.4.930
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
We present here a general model for integrase family site-specific recombination using the geometric relationships of the cleavable phosphodiester bonds and the disposition of the recombinase monomers (defined by their binding planes) with respect to them. The 'oscillation model' is based largely on the conformations of the recombinase-bound DNA duplexes and their dynamics within Holliday junctions. The duplex substrate or the Holliday junction intermediate is capable of 'oscillating' between two cleavage-competent asymmetric states with respect to corresponding chemically inert 'equilibrium positions'. The model accommodates several features of the Flp system and predicts two modes of DNA cleavage during a normal recombination event. It is equally applicable to other systems that mediate recombination across 6, 7 or 8 bp long strand exchange regions (or spacers). The model is consistent with similar to 0-1, 1-2 and 2-3 bp of branch migration during recombination reactions involving 6, 7 and 8 bp spacers, respectively.
引用
收藏
页码:930 / 941
页数:12
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