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细菌中基于RNA对色氨酸合成与降解基因的调控

RNA-based regulation of genes of tryptophan synthesis and degradation, in bacteria.

作者信息

Yanofsky Charles

机构信息

Department of Biological Sciences, Stanford University, Stanford, CA 94305, USA.

出版信息

RNA. 2007 Aug;13(8):1141-54. doi: 10.1261/rna.620507. Epub 2007 Jun 29.

DOI:10.1261/rna.620507
PMID:17601995
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1924887/
Abstract

We are now aware that RNA-based regulatory mechanisms are commonly used to control gene expression in many organisms. These mechanisms offer the opportunity to exploit relatively short, unique RNA sequences, in altering transcription, translation, and/or mRNA stability, in response to the presence of a small or large signal molecule. The ability of an RNA segment to fold and form alternative hairpin secondary structures -- each dedicated to a different regulatory function -- permits selection of specific sequences that can affect transcription and/or translation. In the present paper I will focus on our current understanding of the RNA-based regulatory mechanisms used by Escherichia coli and Bacillus subtilis in controlling expression of the tryptophan biosynthetic operon. The regulatory mechanisms they use for this purpose differ, suggesting that these organisms, or their ancestors, adopted different strategies during their evolution. I will also describe the RNA-based mechanism used by E. coli in regulating expression of its operon responsible for tryptophan degradation, the tryptophanase operon.

摘要

我们现在已经认识到,基于RNA的调控机制在许多生物体中普遍用于控制基因表达。这些机制提供了利用相对较短的独特RNA序列的机会,以响应小或大信号分子的存在来改变转录、翻译和/或mRNA稳定性。RNA片段折叠并形成不同发夹二级结构的能力——每个结构都具有不同的调控功能——允许选择能够影响转录和/或翻译的特定序列。在本文中,我将重点关注我们目前对大肠杆菌和枯草芽孢杆菌用于控制色氨酸生物合成操纵子表达的基于RNA的调控机制的理解。它们用于此目的的调控机制不同,这表明这些生物体或其祖先在进化过程中采用了不同的策略。我还将描述大肠杆菌用于调节其负责色氨酸降解的操纵子(色氨酸酶操纵子)表达的基于RNA的机制。

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本文引用的文献

1
Comparison of tryptophan biosynthetic operon regulation in different Gram-positive bacterial species.不同革兰氏阳性细菌物种中色氨酸生物合成操纵子调控的比较。
Trends Genet. 2007 Sep;23(9):422-6. doi: 10.1016/j.tig.2007.05.005. Epub 2007 Jun 6.
2
Ribosomal features essential for tna operon induction: tryptophan binding at the peptidyl transferase center.对于tna操纵子诱导至关重要的核糖体特征:色氨酸在肽基转移酶中心的结合。
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3
Ribosome recycling factor and release factor 3 action promotes TnaC-peptidyl-tRNA Dropoff and relieves ribosome stalling during tryptophan induction of tna operon expression in Escherichia coli.核糖体循环因子和释放因子3的作用促进TnaC-肽基-tRNA脱落,并在大肠杆菌色氨酸诱导tna操纵子表达过程中缓解核糖体停滞。
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Translation control of trpG from transcripts originating from the folate operon promoter of Bacillus subtilis is influenced by translation-mediated displacement of bound TRAP, while translation control of transcripts originating from a newly identified trpG promoter is not.源自枯草芽孢杆菌叶酸操纵子启动子的转录本对trpG的翻译控制受结合的TRAP的翻译介导置换影响,而源自新鉴定的trpG启动子的转录本的翻译控制则不受此影响。
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RNA polymerase pausing regulates translation initiation by providing additional time for TRAP-RNA interaction.RNA聚合酶暂停通过为TRAP与RNA的相互作用提供额外时间来调节翻译起始。
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6
The trp RNA-binding attenuation protein (TRAP) of Bacillus subtilis regulates translation initiation of ycbK, a gene encoding a putative efflux protein, by blocking ribosome binding.枯草芽孢杆菌的色氨酸RNA结合衰减蛋白(TRAP)通过阻止核糖体结合来调节ycbK(一个编码假定外排蛋白的基因)的翻译起始。
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Changes produced by bound tryptophan in the ribosome peptidyl transferase center in response to TnaC, a nascent leader peptide.结合色氨酸在核糖体肽基转移酶中心响应TnaC(一种新生的前导肽)而产生的变化。
Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3598-603. doi: 10.1073/pnas.0600082103. Epub 2006 Feb 27.
8
Overexpression of tnaC of Escherichia coli inhibits growth by depleting tRNA2Pro availability.大肠杆菌tnaC的过表达通过耗尽tRNA2Pro的可利用性来抑制生长。
J Bacteriol. 2006 Mar;188(5):1892-8. doi: 10.1128/JB.188.5.1892-1898.2006.
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Crystal structure of Bacillus subtilis anti-TRAP protein, an antagonist of TRAP/RNA interaction.枯草芽孢杆菌抗TRAP蛋白(一种TRAP/RNA相互作用的拮抗剂)的晶体结构
Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17600-5. doi: 10.1073/pnas.0508728102. Epub 2005 Nov 23.
10
Complexity in regulation of tryptophan biosynthesis in Bacillus subtilis.枯草芽孢杆菌中色氨酸生物合成调控的复杂性。
Annu Rev Genet. 2005;39:47-68. doi: 10.1146/annurev.genet.39.073003.093745.