TRANSCRIPTION-DRIVEN SITE-SPECIFIC DNA RECOMBINATION INVITRO

被引:44
作者
DROGE, P
机构
[1] Department of Biology, University of Konstanz, W-7750 Konstanz
关键词
SUPERCOILING; TOPOLOGICAL COUPLING; RNA POLYMERASE;
D O I
10.1073/pnas.90.7.2759
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription of a topologically relaxed, circular DNA triggers recombination between two directly repeated res sites by gammadelta resolvase in vitro. This activation of recombination depends on the res site-to-site distance and the orientation of sites with respect to the direction of RNA polymerase tracking. In addition to functioning as a site-specific recombinase, gammadelta resolvase acts as a site-specific topoisomerase and increases the topological linking number of templates during transcription. The data suggest that the link between transcription and recombination could be negative DNA supercoiling that transiently builds up on a relatively short DNA segment in the wake of an advancing RNA polymerase. Surprisingly, transcription-driven recombination is not inhibited by the presence of large amounts of eukaryotic topoisomerase type I, indicating that site-specific recombination can override relaxation by diffusible topoisomerases. This in vitro system might therefore serve as a model for some transcription-directed recombination events observed in vivo.
引用
收藏
页码:2759 / 2763
页数:5
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