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一种源自 3'UTR 的小 RNA 连接肠细菌中的氮代谢和碳代谢。

A 3' UTR-derived small RNA connecting nitrogen and carbon metabolism in enteric bacteria.

机构信息

Division of Molecular and Cellular Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892-4417, USA.

National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.

出版信息

Nucleic Acids Res. 2022 Sep 23;50(17):10093-10109. doi: 10.1093/nar/gkac748.

Abstract

Increasing numbers of small, regulatory RNAs (sRNAs) corresponding to 3' untranslated regions (UTR) are being discovered in bacteria. One such sRNA, denoted GlnZ, corresponds to the 3' UTR of the Escherichia coli glnA mRNA encoding glutamine synthetase. Several forms of GlnZ, processed from the glnA mRNA, are detected in cells growing with limiting ammonium. GlnZ levels are regulated transcriptionally by the NtrC transcription factor and post-transcriptionally by RNase III. Consistent with the expression, E. coli cells lacking glnZ show delayed outgrowth from nitrogen starvation compared to wild type cells. Transcriptome-wide RNA-RNA interactome datasets indicated that GlnZ binds to multiple target RNAs. Immunoblots and assays of fusions confirmed GlnZ-mediated repression of glnP and sucA, encoding proteins that contribute to glutamine transport and the citric acid cycle, respectively. Although the overall sequences of GlnZ from E. coli K-12, Enterohemorrhagic E. coli and Salmonella enterica have significant differences due to various sequence insertions, all forms of the sRNA were able to regulate the two targets characterized. Together our data show that GlnZ impacts growth of E. coli under low nitrogen conditions by modulating genes that affect carbon and nitrogen flux.

摘要

越来越多的与 3' 非翻译区 (UTR) 对应的小调控 RNA (sRNA) 在细菌中被发现。其中一种 sRNA,称为 GlnZ,对应于编码谷氨酰胺合成酶的大肠杆菌 glnA mRNA 的 3' UTR。在有限铵生长的细胞中检测到几种从 glnA mRNA 加工而来的 GlnZ 形式。GlnZ 的水平受 NtrC 转录因子的转录调控和 RNase III 的转录后调控。与表达一致,与野生型细胞相比,缺乏 glnZ 的大肠杆菌细胞从氮饥饿中恢复生长的速度较慢。全转录组 RNA-RNA 相互作用数据集表明,GlnZ 结合到多个靶 RNA 上。免疫印迹和融合实验证实了 GlnZ 对编码参与谷氨酰胺转运和柠檬酸循环的蛋白质的 glnP 和 sucA 的抑制作用。尽管由于各种序列插入,来自大肠杆菌 K-12、肠出血性大肠杆菌和沙门氏菌的 GlnZ 的总体序列有很大差异,但该 sRNA 的所有形式都能够调节所研究的两个靶标。我们的数据表明,GlnZ 通过调节影响碳氮通量的基因来影响大肠杆菌在低氮条件下的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb9/9508815/fe95fec88c37/gkac748figgra1.jpg

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