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Studies of RNA release reaction catalyzed by E. coli transcription termination factor rho using isolated ternary transcription complexes

机译:使用分离的三元转录复合物研究大肠杆菌转录终止因子rho催化的RNA释放反应

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Protein factor rho catalyzes site-specific termination of transcription in a reaction requiring hydrolysis of nucleoside triphosphate with eventual release of RNA from RNA polymerase and DNA template. We have characterized the rho-catalyzed RNA release reaction using isolated transcription complexes. Transcription complexes containing T7 D111 DNA, RNA polymerase, and 3H-labeled nascent RNA were formed and isolated by gel filtration on an Agarose 5M column. When the ternary complexes were incubated with rho factor in the presence of ATP or dATP, significant amounts of nascent RNA were released from the complexes as determined in a membrane filtration assay. Gel electrophoretic analysis of RNA has revealed that rho releases selected species of discrete-sized RNA from among those originally present in the ternary complexes. These results show that rho essentially acts to release RNA from those ternary complexes which have come to pause, and that this reaction proceeds in a discrete step separately from the pausing of RNA synthesis. Under the conditions used, the extent of RNA release widely varied at individual pausing sites and thus the action of rho exhibited certain site-selectivity.
机译:在需要水解三磷酸核苷并最终从RNA聚合酶和DNA模板中释放出RNA的反应中,蛋白质因子rho催化特定位置的转录终止。我们已经表征了使用分离的转录复合物的rho催化的RNA释放反应。形成含有T7 D111 DNA,RNA聚合酶和 3 H标记的新生RNA的转录复合物,并在琼脂糖5M柱上通过凝胶过滤进行分离。当三元复合物在ATP或dATP的存在下与rho因子一起温育时,如在膜过滤试验中确定的那样,复合物中会释放出大量新生RNA。 RNA的凝胶电泳分析表明,rho释放了三元复合物中最初存在的那些离散大小的RNA。这些结果表明,rho本质上起从已经停止的三元复合物中释放RNA的作用,并且该反应在与RNA合成的暂停分开的不连续步骤中进行。在所使用的条件下,RNA的释放程度在各个暂停位点上差异很大,因此rho的作用表现出一定的位点选择性。

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