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本文引用的文献

1
New aspects of RNA-based regulation by Hfq and its partner sRNAs.基于 Hfq 及其伴侣 sRNAs 的 RNA 调控的新方面。
Curr Opin Microbiol. 2018 Apr;42:53-61. doi: 10.1016/j.mib.2017.10.014. Epub 2017 Nov 7.
2
Crosstalk between the tricarboxylic acid cycle and peptidoglycan synthesis in Caulobacter crescentus through the homeostatic control of α-ketoglutarate.通过α-酮戊二酸的稳态控制,新月柄杆菌中三羧酸循环与肽聚糖合成之间的相互作用。
PLoS Genet. 2017 Aug 21;13(8):e1006978. doi: 10.1371/journal.pgen.1006978. eCollection 2017 Aug.
3
RIsearch2: suffix array-based large-scale prediction of RNA-RNA interactions and siRNA off-targets.RIsearch2:基于后缀数组的RNA-RNA相互作用和小干扰RNA脱靶效应的大规模预测
Nucleic Acids Res. 2017 May 5;45(8):e60. doi: 10.1093/nar/gkw1325.
4
GRIL-seq provides a method for identifying direct targets of bacterial small regulatory RNA by in vivo proximity ligation.GRIL-seq提供了一种通过体内邻近连接来鉴定细菌小调控RNA直接靶标的方法。
Nat Microbiol. 2016 Dec 22;2:16239. doi: 10.1038/nmicrobiol.2016.239.
5
Global Mapping of Small RNA-Target Interactions in Bacteria.细菌中小RNA-靶标相互作用的全球图谱
Mol Cell. 2016 Sep 1;63(5):884-97. doi: 10.1016/j.molcel.2016.07.026.
6
An intracellular compass spatially coordinates cell cycle modules in Caulobacter crescentus.一种细胞内罗盘在新月柄杆菌中对细胞周期模块进行空间协调。
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7
Transcriptomic analysis of the stationary phase response regulator SpdR in Caulobacter crescentus.新月柄杆菌中稳定期响应调节因子SpdR的转录组学分析。
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8
Global RNA recognition patterns of post-transcriptional regulators Hfq and CsrA revealed by UV crosslinking in vivo.通过体内紫外线交联揭示转录后调控因子Hfq和CsrA的全局RNA识别模式。
EMBO J. 2016 May 2;35(9):991-1011. doi: 10.15252/embj.201593360. Epub 2016 Apr 4.
9
Alternative Hfq-sRNA interaction modes dictate alternative mRNA recognition.替代性Hfq-sRNA相互作用模式决定了替代性mRNA识别。
EMBO J. 2015 Oct 14;34(20):2557-73. doi: 10.15252/embj.201591569. Epub 2015 Sep 15.
10
The global regulatory architecture of transcription during the Caulobacter cell cycle.柄杆菌细胞周期中转录的全球调控架构。
PLoS Genet. 2015 Jan 8;11(1):e1004831. doi: 10.1371/journal.pgen.1004831. eCollection 2015 Jan.

新月柄杆菌中 Hfq 结合 RNA 的鉴定。

Identification of Hfq-binding RNAs in Caulobacter crescentus.

机构信息

a Departamento de Microbiologia, Instituto de Ciências Biomédicas , Universidade de São Paulo , São Paulo , Brazil.

b Biozentrum , University of Basel , Basel , Switzerland.

出版信息

RNA Biol. 2019 Jun;16(6):719-726. doi: 10.1080/15476286.2019.1593091. Epub 2019 Mar 26.

DOI:10.1080/15476286.2019.1593091
PMID:30870072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6546397/
Abstract

Small RNAs are important for post-transcriptional regulation of gene expression, affecting stability and activity of their target mRNAs. The bacterial Sm-like protein Hfq is required to promote pairing between both RNAs when their sequence complementarity is limited. To provide a first global view on the post-transcriptional landscape of the α-proteobacterium Caulobacter crescentus, we have identified the Hfq-binding RNAs employing High-throughput sequencing of RNA isolated by cross-linking immunoprecipitation (HITS-CLIP). A total of 261 RNAs, including 3 unannotated RNAs, were successfully identified and classified according to putative function. Moreover, possible interactions between the identified sRNAs with mRNA targets were postulated through computational target predictions.

摘要

小 RNA 对于基因表达的转录后调控非常重要,影响其靶 mRNA 的稳定性和活性。当 RNA 序列互补性有限时,细菌 Sm 样蛋白 Hfq 对于促进两者之间的配对是必需的。为了首次提供α变形菌新月柄杆菌转录后景观的全局视图,我们通过交联免疫沉淀(HITS-CLIP)分离的 RNA 进行高通量测序,鉴定了 Hfq 结合的 RNA。总共鉴定出 261 个 RNA,包括 3 个未注释的 RNA,根据推测的功能进行了分类。此外,通过计算靶预测,提出了所鉴定的 sRNA 与 mRNA 靶之间可能的相互作用。