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CroS 是 λ Cro 阻遏物的同源物,在抑制 polV 依赖性诱变中起主要作用。

CroS , an ortholog of the λ Cro repressor, plays a major role in suppressing polV -dependent mutagenesis.

机构信息

Laboratory of Genomic Integrity, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.

Department of Biology, Southwestern University, Georgetown, TX, USA.

出版信息

Mol Microbiol. 2021 Sep;116(3):877-889. doi: 10.1111/mmi.14777. Epub 2021 Jul 12.

DOI:10.1111/mmi.14777
PMID:34184328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8460599/
Abstract

When subcloned into low-copy-number expression vectors, rumAB, encoding polV (RumA' B), is best characterized as a potent mutator giving rise to high levels of spontaneous mutagenesis in vivo. This is in dramatic contrast to the poorly mutable phenotype when polV is expressed from the native 88.5 kb R391, suggesting that R391 expresses cis-acting factors that suppress the expression and/or the activity of polV . Indeed, we recently discovered that SetR , an ortholog of λ cI repressor, is a transcriptional repressor of rumAB. Here, we report that CroS , an ortholog of λ Cro, also serves as a potent transcriptional repressor of rumAB. Levels of RumA are dependent upon an interplay between SetR and CroS , with the greatest reduction of RumA protein levels observed in the absence of SetR and the presence of CroS . Under these conditions, CroS completely abolishes the high levels of mutagenesis promoted by polV expressed from low-copy-number plasmids. Furthermore, deletion of croS on the native R391 results in a dramatic increase in mutagenesis, indicating that CroS plays a major role in suppressing polV mutagenesis in vivo. Inactivating mutations in CroS therefore have the distinct possibility of increasing cellular mutagenesis that could lead to the evolution of antibiotic resistance of pathogenic bacteria harboring R391.

摘要

当亚克隆到低拷贝数表达载体中时,编码 polV( RumA' B)的 rumAB 被最好地描述为一种强大的诱变剂,在体内导致高水平的自发突变。这与 polV 从天然的 88.5kb R391 表达时突变表型很差形成鲜明对比,表明 R391 表达顺式作用因子抑制 polV 的表达和/或活性。事实上,我们最近发现,λ cI 阻遏物的同源物 SetR 是 rumAB 的转录阻遏物。在这里,我们报告说,λ Cro 的同源物 CroS 也是 rumAB 的有效转录阻遏物。 RumA 的水平取决于 SetR 和 CroS 之间的相互作用,在没有 SetR 和存在 CroS 的情况下观察到 RumA 蛋白水平的最大降低。在这些条件下,CroS 完全消除了低拷贝数质粒表达的 polV 促进的高水平诱变。此外,在天然 R391 上缺失 croS 会导致突变率急剧增加,表明 CroS 在体内抑制 polV 突变中起主要作用。因此,CroS 的失活突变很有可能增加细胞突变率,导致携带 R391 的致病性细菌对抗生素耐药性的进化。

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Adv Genet. 2020;105:229-292. doi: 10.1016/bs.adgen.2019.12.002. Epub 2020 May 6.
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Isolation, nucleotide sequencing and genomic comparison of a Novel SXT/R391 ICE mobile genetic element isolated from a municipal wastewater environment.从城市废水环境中分离出的一种新型 SXT/R391 ICE 移动遗传元件的分离、核苷酸测序和基因组比较。
Sci Rep. 2020 May 26;10(1):8716. doi: 10.1038/s41598-020-65216-5.
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Integration of the blaNDM-1 carbapenemase gene into a novel SXT/R391 integrative and conjugative element in Proteus vulgaris.
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Sending out an SOS - the bacterial DNA damage response.发出求救信号——细菌的DNA损伤反应。
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