Ahmad Sohail, Huang Qihong, Ni Jinfeng, Xiao Yuanxi, Yang Yunfeng, Shen Yulong
CRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Microbial Technology Institute, Shandong University, Qingdao, China.
Front Microbiol. 2020 Dec 1;11:607431. doi: 10.3389/fmicb.2020.607431. eCollection 2020.
EndoMS is a recently identified mismatch specific endonuclease in Thermococcales of Archaea and Mycobacteria of Bacteria. The homologs of EndoMS are conserved in Archaea and Actinobacteria, where classic MutS-MutL-mediated DNA mismatch repair pathway is absent or non-functional. Here, we report a study on the mismatch cleavage activity and function of an EndoMS homolog (SisEndoMS) from REY15A, the model archaeon belonging to Crenarchaeota. SisEndoMS is highly active on duplex DNA containing G/T, G/G, and T/T mismatches. Interestingly, the cleavage activity of SisEndoMS is stimulated by the heterotrimeric PCNAs, and when Mn was used as the co-factor instead of Mg, SisEndoMS was also active on DNA substrates containing C/T or A/G mismatches, suggesting that the endonuclease activity can be regulated by ion co-factors and accessory proteins. We compared the spontaneous mutation rate of the wild type strain REY15A and ∆ by counter selection against 5-fluoroorotic acid (5-FOA). The knockout mutant had much higher spontaneous mutation rate (5.06 × 10) than that of the wild type (4.6 × 10). A mutation accumulation analysis also showed that the deletion mutant had a higher mutation occurrence than the wild type, with transition mutation being the dominant, suggesting that SisEndoMS is responsible for mutation avoidance in this hyperthermophilic archaeon. Overexpression of the wild type SisEndoMS in resulted in retarded growth and abnormal cell morphology, similar to strains overexpressing Hje and Hjc, the Holliday junction endonucleases. Transcriptomic analysis revealed that SisEndoMS overexpression led to upregulation of distinct gene including the CRISPR-Cas IIIB system, methyltransferases, and glycosyltransferases, which are mainly localized to specific regions in the chromosome. Collectively, our results support that EndoMS proteins represent a noncanonical DNA repair pathway in Archaea. The mechanism of the mismatch repair pathway in which have a single chromosome is discussed.
EndoMS是最近在古菌的嗜热栖热菌属和细菌的分枝杆菌中鉴定出的一种错配特异性核酸内切酶。EndoMS的同源物在古菌和放线菌中保守,而在这些菌中经典的MutS-MutL介导的DNA错配修复途径不存在或无功能。在此,我们报道了一项关于来自泉古菌门的模式古菌REY15A的EndoMS同源物(SisEndoMS)的错配切割活性和功能的研究。SisEndoMS对含有G/T、G/G和T/T错配的双链DNA具有高活性。有趣的是,异源三聚体增殖细胞核抗原(PCNA)可刺激SisEndoMS的切割活性,并且当使用锰作为辅助因子而非镁时,SisEndoMS对含有C/T或A/G错配的DNA底物也有活性,这表明核酸内切酶活性可受离子辅助因子和辅助蛋白调控。我们通过针对5-氟乳清酸(5-FOA)的反选择来比较野生型菌株REY15A和缺失突变体的自发突变率。缺失突变体的自发突变率(5.06×10)比野生型(4.6×10)高得多。突变积累分析还表明,缺失突变体的突变发生率高于野生型,其中转换突变占主导,这表明SisEndoMS负责该嗜热古菌中的突变避免。野生型SisEndoMS在[此处原文缺失相关菌株信息]中的过表达导致生长迟缓以及细胞形态异常,类似于过表达Holliday连接点核酸内切酶Hje和Hjc的菌株。转录组分析显示,SisEndoMS的过表达导致包括CRISPR-Cas IIIB系统、甲基转移酶和糖基转移酶在内的不同基因上调,这些基因主要定位于染色体的特定区域。总体而言,我们的结果支持EndoMS蛋白代表古菌中的一种非经典DNA修复途径。文中还讨论了具有单条染色体的[此处原文缺失相关菌属信息]中的错配修复途径机制。