[SigE inhibits DNA damage and participates in the regulation of DNA damage repair in Mycobacterium smegmatis].

Jialing Tang, Zhiying Li, Nan Lu, Jiajia Bao, Xia Tang, Junzhuo Si, Huichao Fu, Anlong Li, Lei Xu, Chun Yang, Yonglin He
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Abstract

Objective To investigate the anti-DNA damage role of Sigma factor E (SigE) and its regulation mechanism of DNA damage repair in Mycobacterium smegmatis(MS). Methods The SigE gene of Mycobacterium smegmatis was cloned into plasmid pMV261 to construct recombinant plasmid pMV261(+)-SigE, and the inserted gene was verified by sequencing. The recombinant plasmid was electrically transformed into Mycobacterium smegmatis to construct SigE over-expression strain, and the expression of SigE was detected by Western blot analysis. The Mycobacterium smegmatis containing pMV261 plasmid was used as the control strain. Growth differences between the two stains were monitored by measuring the 600 nm absorbance (A600) value of the bacterial culture suspension. The survival rate differences between two kinds of strains which were treated with three kinds of DNA damaging agents including ultraviolet ray (UV), cisplatin (DDP), and mitomycin C (MMC) were detected by colony forming unit (CFU) counting assay. DNA damage repair pathways of Mycobacteria were analyzed through bioinformatics and SigE-related genes were screened. The relative expression levels of these genes possibly related to the SigE against DNA damage were detected by real-time fluorescence quantitative PCR. Results SigE over-expression strain pMV261(+)-SigE/MS was constructed and the expression of SigE in Mycobacterium smegmatis was detected. Compared with the control strain, the SigE over-expression strain grew more slowly and entered the growth plateau later; survival rate analysis found that SigE over-expression strain was more resistant to three DNA damaging agents including UV, DDP, and MMC. Bioinformatic analysis indicated that SigE gene was closely related to DNA damage repair genes recA, single-strand DNA binding protein, (ssb), and dnaE2; the expression levels of recA, dnaE2, and ssb in SigE over-expression strain all increased with varying degrees compared with those in the control strain. Conclusion SigE plays an important role in inhibiting the DNA damage of Mycobacterium smegmatis, whose mechanism is closely related to the regulation of DNA damage repair.

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[SigE抑制耻垢分枝杆菌DNA损伤并参与DNA损伤修复的调控]。
目的探讨Sigma因子E (SigE)在耻垢分枝杆菌(MS)中抗DNA损伤的作用及其对DNA损伤修复的调控机制。方法将耻垢分枝杆菌SigE基因克隆到质粒pMV261中,构建重组质粒pMV261(+)-SigE,并对插入的基因进行测序验证。将重组质粒电转化耻垢分枝杆菌,构建SigE过表达菌株,Western blot检测SigE的表达。以含pMV261质粒的耻垢分枝杆菌为对照菌株。通过测定细菌培养悬浮液的600 nm吸光度(A600)值来监测两种菌株的生长差异。采用菌落形成单位(CFU)计数法检测紫外线(UV)、顺铂(DDP)和丝裂霉素C (MMC)三种DNA损伤剂对两种菌株的存活率差异。应用生物信息学方法分析分枝杆菌DNA损伤修复途径,筛选sige相关基因。实时荧光定量PCR检测这些可能与SigE有关的基因对DNA损伤的相对表达量。结果构建SigE过表达菌株pMV261(+)-SigE/MS,检测SigE在耻垢分枝杆菌中的表达。与对照菌株相比,SigE过表达菌株生长较慢,进入生长平台期较晚;存活率分析发现SigE过表达菌株对UV、DDP和MMC三种DNA损伤剂的抗性更强。生物信息学分析表明,SigE基因与DNA损伤修复基因recA、单链DNA结合蛋白(ssb)、dnaE2密切相关;SigE过表达菌株中recA、dnaE2和ssb的表达量均较对照菌株有不同程度的升高。结论SigE在抑制耻垢分枝杆菌DNA损伤中起重要作用,其机制与调控DNA损伤修复密切相关。
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