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基于转录组分析的 LexA 对 中 UV 诱导的 SOS 反应的调控。

The Regulation of LexA on UV-Induced SOS Response in Based on Transcriptome Analysis.

机构信息

State Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong University, Qingdao 266237, P.R. China.

出版信息

J Microbiol Biotechnol. 2021 Jul 28;31(7):912-920. doi: 10.4014/jmb.2103.03047.

Abstract

SOS response is a conserved response to DNA damage in prokaryotes and is negatively regulated by LexA protein, which recognizes specifically an "SOS-box" motif present in the promoter region of SOS genes. DK1622 possesses a gene, and while the deletion of had no significant effect on either bacterial morphology, UV-C resistance, or sporulation, it did delay growth. UV-C radiation resulted in 651 upregulated genes in , including the typical SOS genes , , , and so on, mostly enriched in the pathways of DNA replication and repair, secondary metabolism, and signal transduction. The UV-irradiated mutant also showed the induced expression of SOS genes and these SOS genes enriched into a similar pathway profile to that of wild-type strain. Without irradiation treatment, the absence of LexA enhanced the expression of 122 genes that were not enriched in any pathway. Further analysis of the promoter sequence revealed that in the 122 genes, only the promoters of , and an operon composed of three genes (, and ) had SOS box sequence to which the LexA protein is bound directly. These results update our current understanding of SOS response in and show that UV induces more genes involved in secondary metabolism and signal transduction in addition to DNA replication and repair; and while the canonical LexA-dependent regulation on SOS response has shrunk, only 5 SOS genes are directly repressed by LexA.

摘要

SOS 响应是原核生物中对 DNA 损伤的保守反应,受 LexA 蛋白的负调控,LexA 蛋白特异性识别 SOS 基因启动子区域中存在的“ SOS 盒”基序。DK1622 拥有一个 基因,虽然该基因的缺失对细菌形态、UV-C 抗性或孢子形成没有显著影响,但它确实延迟了生长。UV-C 辐射导致 中 651 个上调基因,包括典型的 SOS 基因 、 、 等,主要富集在 DNA 复制和修复、次生代谢和信号转导途径中。受 UV 照射的 突变体也表现出 SOS 基因的诱导表达,这些 SOS 基因富集到与野生型菌株相似的途径谱中。在没有照射处理的情况下,LexA 的缺失增强了 122 个未富集到任何途径的基因的表达。对启动子序列的进一步分析表明,在这 122 个基因中,只有 、 和由三个基因( 、 和 )组成的操纵子的启动子具有 LexA 蛋白直接结合的 SOS 盒序列。这些结果更新了我们对 中 SOS 反应的现有认识,并表明除了 DNA 复制和修复之外,UV 还诱导更多参与次生代谢和信号转导的基因;尽管经典的 LexA 依赖性 SOS 反应调节已经缩小,但只有 5 个 SOS 基因直接受到 LexA 的抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1c9/9705874/d279a2fd68e1/jmb-31-7-912-f1.jpg

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