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转录暂停协调适体结构域和核酶表达平台的折叠。

Transcriptional pausing coordinates folding of the aptamer domain and the expression platform of a riboswitch.

机构信息

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3323-8. doi: 10.1073/pnas.1113086109. Epub 2012 Feb 13.

Abstract

Riboswitches are cis-acting elements that regulate gene expression by affecting transcriptional termination or translational initiation in response to binding of a metabolite. A typical riboswitch is made of an upstream aptamer domain and a downstream expression platform. Both domains participate in the folding and structural rearrangement in the absence or presence of its cognate metabolite. RNA polymerase pausing is a fundamental property of transcription that can influence RNA folding. Here we show that pausing plays an important role in the folding and conformational rearrangement of the Escherichia coli btuB riboswitch during transcription by the E. coli RNA polymerase. This riboswitch consists of an approximately 200 nucleotide, coenzyme B12 binding aptamer domain and an approximately 40 nucleotide expression platform that controls the ribosome access for translational initiation. We found that transcriptional pauses at strategic locations facilitate folding and structural rearrangement of the full-length riboswitch, but have minimal effect on the folding of the isolated aptamer domain. Pausing at these regulatory sites blocks the formation of alternate structures and plays a chaperoning role that couples folding of the aptamer domain and the expression platform. Pausing at strategic locations may be a general mechanism for coordinated folding and conformational rearrangements of riboswitch structures that underlie their response to environmental cues.

摘要

核糖开关是通过结合代谢物来影响转录终止或翻译起始从而调节基因表达的顺式作用元件。一个典型的核糖开关由上游适配体结构域和下游表达平台组成。这两个结构域都参与了没有或存在其同源代谢物时的折叠和结构重排。RNA 聚合酶暂停是转录的一个基本特性,它可以影响 RNA 的折叠。在这里,我们展示了在大肠杆菌 RNA 聚合酶转录过程中,p 因子暂停在大肠杆菌 btuB 核糖开关的折叠和构象重排中起着重要作用。这个核糖开关由大约 200 个核苷酸的钴胺素 B12 结合适配体结构域和大约 40 个核苷酸的表达平台组成,它控制着核糖体进入翻译起始。我们发现,在战略位置的转录暂停促进了全长核糖开关的折叠和结构重排,但对分离的适配体结构域的折叠影响很小。在这些调节位点的暂停阻止了替代结构的形成,并发挥了伴侣作用,将适配体结构域和表达平台的折叠偶联起来。在战略位置的暂停可能是协调核糖开关结构折叠和构象重排的一般机制,这是它们对环境线索做出反应的基础。

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