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RNA解旋酶CshA的C末端区域是与机会致病菌金黄色葡萄球菌中的降解体相互作用以及大量RNA周转所必需的。

The C-terminal region of the RNA helicase CshA is required for the interaction with the degradosome and turnover of bulk RNA in the opportunistic pathogen Staphylococcus aureus.

作者信息

Giraud Caroline, Hausmann Stéphane, Lemeille Sylvain, Prados Julien, Redder Peter, Linder Patrick

机构信息

a Department of Microbiology and Molecular Medicine ; Medical Faculty; University of Geneva ; Michel Servet , Geneva , Switzerland.

出版信息

RNA Biol. 2015;12(6):658-74. doi: 10.1080/15476286.2015.1035505.

DOI:10.1080/15476286.2015.1035505
PMID:25997461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4615653/
Abstract

Staphylococcus aureus is a versatile opportunistic pathogen that adapts readily to a variety of different growth conditions. This adaptation requires a rapid regulation of gene expression including the control of mRNA abundance. The CshA DEAD-box RNA helicase was previously shown to be required for efficient turnover of the agr quorum sensing mRNA. Here we show by transcriptome-wide RNA sequencing and microarray analyses that CshA is required for the degradation of bulk mRNA. Moreover a subset of mRNAs is significantly stabilised in absence of CshA. Deletion of the C-terminal extension affects RNA turnover similar to the full deletion of the cshA gene. In accordance with RNA decay data, the C-terminal region of CshA is required for an RNA-independent interaction with components of the RNA degradation machinery. The C-terminal truncation of CshA reduces its ATPase activity and this reduction cannot be compensated at high RNA concentrations. Finally, the deletion of the C-terminal extension does affect growth at low temperatures, but to a significantly lesser degree than the full deletion, indicating that the core of the helicase can assume a partial function and opening the possibility that CshA is involved in different cellular processes.

摘要

金黄色葡萄球菌是一种适应性很强的机会致病菌,能够轻松适应各种不同的生长条件。这种适应需要对基因表达进行快速调控,包括对mRNA丰度的控制。先前已证明CshA DEAD盒RNA解旋酶是群体感应mRNA高效周转所必需的。在这里,我们通过全转录组RNA测序和微阵列分析表明,CshA是大量mRNA降解所必需的。此外,在缺乏CshA的情况下,一部分mRNA会显著稳定。C端延伸的缺失对RNA周转的影响与cshA基因的完全缺失相似。根据RNA衰变数据,CshA的C端区域是与RNA降解机制的成分进行RNA非依赖性相互作用所必需的。CshA的C端截短会降低其ATP酶活性,并且这种降低在高RNA浓度下无法得到补偿。最后,C端延伸的缺失确实会影响低温下的生长,但程度明显小于完全缺失,这表明解旋酶的核心可以发挥部分功能,并开启了CshA参与不同细胞过程的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/83cff9594540/krnb-12-06-1035505-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/308dce0f5bff/krnb-12-06-1035505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/4cb29dddb262/krnb-12-06-1035505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/26057ef12fa8/krnb-12-06-1035505-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/fc676d4702e1/krnb-12-06-1035505-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/83cff9594540/krnb-12-06-1035505-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/308dce0f5bff/krnb-12-06-1035505-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/4cb29dddb262/krnb-12-06-1035505-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/26057ef12fa8/krnb-12-06-1035505-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/fc676d4702e1/krnb-12-06-1035505-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20d7/4615653/83cff9594540/krnb-12-06-1035505-g005.jpg

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