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本文引用的文献

1
Regulation by small RNAs in bacteria: expanding frontiers.细菌中小 RNA 的调控:拓展前沿。
Mol Cell. 2011 Sep 16;43(6):880-91. doi: 10.1016/j.molcel.2011.08.022.
2
Discriminating tastes: physiological contributions of the Hfq-binding small RNA Spot 42 to catabolite repression.区分味道:Hfq 结合小 RNA Spot 42 对分解代谢物阻遏的生理贡献。
RNA Biol. 2011 Sep-Oct;8(5):766-70. doi: 10.4161/rna.8.5.16024. Epub 2011 Jul 26.
3
Small RNAs endow a transcriptional activator with essential repressor functions for single-tier control of a global stress regulon.小 RNA 赋予转录激活因子必要的抑制功能,用于全局应激调控子的单层控制。
Proc Natl Acad Sci U S A. 2011 Aug 2;108(31):12875-80. doi: 10.1073/pnas.1109379108. Epub 2011 Jul 18.
4
Hfq and its constellation of RNA.Hfq 及其 RNA 伴侣。
Nat Rev Microbiol. 2011 Aug 15;9(8):578-89. doi: 10.1038/nrmicro2615.
5
Quantifying the sequence-function relation in gene silencing by bacterial small RNAs.量化细菌小 RNA 基因沉默中的序列-功能关系。
Proc Natl Acad Sci U S A. 2011 Jul 26;108(30):12473-8. doi: 10.1073/pnas.1100432108. Epub 2011 Jul 8.
6
Pervasive post-transcriptional control of genes involved in amino acid metabolism by the Hfq-dependent GcvB small RNA.Hfq 依赖的 GcvB 小 RNA 对参与氨基酸代谢的基因进行普遍的转录后调控。
Mol Microbiol. 2011 Sep;81(5):1144-65. doi: 10.1111/j.1365-2958.2011.07751.x. Epub 2011 Jul 27.
7
RNApredator: fast accessibility-based prediction of sRNA targets.RNApredator:基于快速可及性的 sRNA 靶标预测。
Nucleic Acids Res. 2011 Jul;39(Web Server issue):W149-54. doi: 10.1093/nar/gkr467. Epub 2011 Jun 14.
8
Enzymatic assembly of overlapping DNA fragments.重叠DNA片段的酶促组装
Methods Enzymol. 2011;498:349-61. doi: 10.1016/B978-0-12-385120-8.00015-2.
9
Versatile RNA-sensing transcriptional regulators for engineering genetic networks.多功能 RNA 感应转录调控因子用于工程遗传网络。
Proc Natl Acad Sci U S A. 2011 May 24;108(21):8617-22. doi: 10.1073/pnas.1015741108. Epub 2011 May 9.
10
The base-pairing RNA spot 42 participates in a multioutput feedforward loop to help enact catabolite repression in Escherichia coli.碱基配对 RNA 斑点 42 参与多输出前馈回路,有助于在大肠杆菌中实施分解代谢物阻遏。
Mol Cell. 2011 Feb 4;41(3):286-97. doi: 10.1016/j.molcel.2010.12.027.

多种因素决定了 Hfq 结合小 RNA 的靶标选择。

Multiple factors dictate target selection by Hfq-binding small RNAs.

机构信息

Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.

出版信息

EMBO J. 2012 Apr 18;31(8):1961-74. doi: 10.1038/emboj.2012.52. Epub 2012 Mar 2.

DOI:10.1038/emboj.2012.52
PMID:22388518
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3343335/
Abstract

Hfq-binding small RNAs (sRNAs) in bacteria modulate the stability and translational efficiency of target mRNAs through limited base-pairing interactions. While these sRNAs are known to regulate numerous mRNAs as part of stress responses, what distinguishes targets and non-targets among the mRNAs predicted to base pair with Hfq-binding sRNAs is poorly understood. Using the Hfq-binding sRNA Spot 42 of Escherichia coli as a model, we found that predictions using only the three unstructured regions of Spot 42 substantially improved the identification of previously known and novel Spot 42 targets. Furthermore, increasing the extent of base-pairing in single or multiple base-pairing regions improved the strength of regulation, but only for the unstructured regions of Spot 42. We also found that non-targets predicted to base pair with Spot 42 lacked an Hfq-binding site, folded into a secondary structure that occluded the Spot 42 targeting site, or had overlapping Hfq-binding and targeting sites. By modifying these features, we could impart Spot 42 regulation on non-target mRNAs. Our results thus provide valuable insights into the requirements for target selection by sRNAs.

摘要

细菌中的 Hfq 结合小 RNA(sRNA)通过有限的碱基配对相互作用调节靶 mRNA 的稳定性和翻译效率。虽然这些 sRNA 被认为是作为应激反应的一部分调节众多 mRNA,但对于预测与 Hfq 结合 sRNA 碱基配对的 mRNA 中哪些是靶标,哪些是非靶标,了解甚少。我们以大肠杆菌的 Hfq 结合 sRNA Spot 42 为模型,发现仅使用 Spot 42 的三个无结构区域的预测可以显著提高先前已知和新的 Spot 42 靶标的识别。此外,增加单个或多个碱基配对区域的碱基配对程度可以增强调控强度,但仅针对 Spot 42 的无结构区域。我们还发现,预测与 Spot 42 碱基配对的非靶标缺乏 Hfq 结合位点,折叠成一种二级结构,阻断了 Spot 42 的靶标位点,或者具有重叠的 Hfq 结合和靶标位点。通过修饰这些特征,我们可以将 Spot 42 的调控赋予非靶标 mRNA。因此,我们的研究结果为 sRNA 靶标选择的要求提供了有价值的见解。