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毒力质粒pXO1中由AtxA控制的小RNA调控基因表达。

AtxA-Controlled Small RNAs of Virulence Plasmid pXO1 Regulate Gene Expression .

作者信息

Corsi Ileana D, Dutta Soumita, van Hoof Ambro, Koehler Theresa M

机构信息

Department of Microbiology and Molecular Genetics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, United States.

MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, The University of Texas, Houston, TX, United States.

出版信息

Front Microbiol. 2021 Jan 15;11:610036. doi: 10.3389/fmicb.2020.610036. eCollection 2020.

Abstract

Small regulatory RNAs (sRNAs) are short transcripts that base-pair to mRNA targets or interact with regulatory proteins. sRNA function has been studied extensively in Gram-negative bacteria; comparatively less is known about sRNAs in Firmicutes. Here we investigate two sRNAs encoded by virulence plasmid pXO1 of , the causative agent of anthrax. The sRNAs, named "XrrA and XrrB" (for pXO1-encoded regulatory RNA) are abundant and highly stable primary transcripts, whose expression is dependent upon AtxA, the master virulence regulator of . sRNA levels are highest during culture conditions that promote AtxA expression and activity, and sRNA levels are unaltered in Hfq RNA chaperone null-mutants. Comparison of the transcriptome of a virulent Ames-derived strain to the transcriptome of isogenic sRNA-null mutants revealed multiple 4.0- to >100-fold differences in gene expression. Most regulatory effects were associated with XrrA, although regulation of some transcripts suggests functional overlap between the XrrA and XrrB. Many sRNA-regulated targets were chromosome genes associated with branched-chain amino acid metabolism, proteolysis, and transmembrane transport. Finally, in a mouse model for systemic anthrax, the lungs and livers of animals infected with -null mutants had a small reduction in bacterial burden, suggesting a role for XrrA in pathogenesis.

摘要

小调控RNA(sRNA)是与mRNA靶标碱基配对或与调控蛋白相互作用的短转录本。sRNA的功能已在革兰氏阴性菌中得到广泛研究;相比之下,对于厚壁菌门中的sRNA了解较少。在这里,我们研究了炭疽病病原体 毒力质粒pXO1编码的两种sRNA。这两种sRNA名为“XrrA和XrrB”(pXO1编码的调控RNA),是丰富且高度稳定的初级转录本,其表达依赖于 主要毒力调节因子AtxA。在促进AtxA表达和活性的培养条件下,sRNA水平最高,并且在Hfq RNA伴侣蛋白缺失突变体中sRNA水平未改变。将毒力Ames衍生菌株的转录组与同基因sRNA缺失突变体的转录组进行比较,发现基因表达存在多个4.0至>100倍的差异。大多数调控作用与XrrA相关,尽管对一些转录本的调控表明XrrA和XrrB之间存在功能重叠。许多受sRNA调控的靶标是与支链氨基酸代谢、蛋白水解和跨膜运输相关的染色体基因。最后,在系统性炭疽病小鼠模型中,感染 缺失突变体的动物的肺和肝脏中的细菌载量略有降低,这表明XrrA在 发病机制中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de97/7843513/e978bcf2c292/fmicb-11-610036-g001.jpg

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