The antiterminator NusB enhances termination at a sub-optimal Rho site

被引:6
作者
Carlomagno, MS
Nappo, A
机构
[1] Univ Naples Federico II, Dipartimento Biol & Patol Cellulare & Mol L Calif, I-80131 Naples, Italy
[2] CNR, Ctr Endocrinol & Oncol Sperimentale G Salvatore, I-80131 Naples, Italy
关键词
boxA; his operon; polarity; Rho-dependent termination; rut sites;
D O I
10.1006/jmbi.2001.4678
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
Interactions between the antiterminator NusB and boxA elements in the nut sites are necessary to ensure lambda N-mediated processive antitermination. Similarly, in the bacterial cell, interactions between NusB and boxA elements help RNA polymerase to counteract polarity during transcription of rm operons. We analyzed the effects of NusB on intragenic termination at the level of two tandem terminators located in the hisG cistron, GTTE1 and GTTE2. Unexpectedly, we found that NusB enhances transcription termination at the sub-optimal Rho site GT'TE1. Moreover, site-directed mutagenesis of a boxA homolog located within GTTE1 and the masking of this element by translating ribosomes demonstrated that the recruitment of NusB in the termination complex is mediated by a boxA element. The mutated boxA also abolishes the formation of a NusB-dependent complex on GTTE1 RNA. On the whole, results provide evidence that interactions between NusB and boxA can enhance Rho-dependent termination. (C) 2001 Academic Press.
引用
收藏
页码:19 / 28
页数:10
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