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Regulatory interplay between small RNAs and transcription termination factor Rho

机译:小RNA和转录终止因子RHO之间的监管相互作用

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摘要

The largest and best studied group of regulatory small RNAs (sRNAs) in bacteria act by modulating translation or turnover of messenger RNAs (mRNAs) through base-pairing interactions that typically take place near the 5' end of the mRNA. This allows the sRNA to bind the complementary target sequence while the remainder of the mRNA is still being made, creating conditions whereby the action of the sRNA can extend to transcriptional steps, most notably transcription termination. Increasing evidence corroborates the existence of a functional interplay between sRNAs and termination factor Rho. Two general mechanisms have emerged. One mechanism operates in translated regions subjected to sRNA repression. By inhibiting ribosome binding co-transcriptionally, the sRNA uncouples translation from transcription, allowing Rho to bind the nascent RNA and promote termination. In the second mechanism, which functions in 5' untranslated regions, the sRNA antagonizes termination directly by interfering with Rho binding to the RNA or the subsequent translocation along the RNA. Here, we review the above literature in the context of other mechanisms that underlie the participation of Rho-dependent transcription termination in gene regulation. This article is part of a Special Issue entitled: RNA and gene control in bacteria edited by Dr. M. Guillier and F. Repoila.
机译:通过调节Messenger RNA(MRNA)的转换或转换通过通常在mRNA的5'末端附近进行的碱基配对相互作用调节或营业额来对细菌的最大和最佳学习的小rNA(srnas)。这允许SRNA结合互补靶序列,同时仍在进行MRNA的剩余部分,产生SRNA的作用可以延伸到转录步骤的条件,最值得注意的转录终止。越来越多的证据证实了SRNA和终止因子RHO之间的功能相互作用的存在。出现了两种一般机制。一种机制在经过SRNA抑制的转化区域中运行。通过抑制核糖体结合同步,SRNA与转录的翻译源,允许rho结合新生的RNA并促进终止。在第二种机制中,在5'未转换区域中起作用,SRNA通过干扰与RNA的RHO结合或随后沿RNA的易位而直接拮抗终止。在这里,我们在其他机制的背景下审查了上述文献,这使得RHO依赖性转录终止在基因调节中的参与。本文是标题的特殊问题的一部分:由M. Guillier博士和F. repoila编辑的细菌中的RNA和基因对照。

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