Huang Qinqin, Luo Hongping, Liu Minqiang, Zeng Jie, Abdalla Abualgasim Elgaili, Duan Xiangke, Li Qiming, Xie Jianping
Institute of Modern Biopharmaceuticals, State Key Laboratory Breeding Base of Eco-Environment and Bio-Resource of the Three Gorges Area, Key Laboratory of Ministry of Education Eco-Environment of the Three Gorges Reservoir Region, School of Life Sciences, Southwest University, Chongqing 400715, China.
Institute of Modern Biopharmaceuticals, State Key Laboratory Breeding Base of Eco-Environment and Bio-Resource of the Three Gorges Area, Key Laboratory of Ministry of Education Eco-Environment of the Three Gorges Reservoir Region, School of Life Sciences, Southwest University, Chongqing 400715, China.
Infect Genet Evol. 2016 Jun;40:295-301. doi: 10.1016/j.meegid.2015.10.019. Epub 2015 Oct 22.
Clustered regularly interspaced short palindromic repeats (CRISPR) are present in the genome of 40% bacteria and 90% archaea. CRISPR and accompanying Cas proteins constitute an adaptive immune system against disruptive mobile genetic elements. Two CRISPRs and 9 genes encoding CRISPR-associated proteins have been found in the genome of Mycobacterium tuberculosis. The CRISPR-associated Cas2 is an endoribonuclease required for the acquisition of new spacers. In this study, Cas2 encoded by Rv2816c was expressed in Mycobacterium smegmatis lacking CRISPR-Cas system and its role in stress responses of M. smegmatis in vitro and within macrophages was studied. We found that Cas2 mediated M. smegmatis stress response changes were associated with the altered expression of sigma factors which involved in mycobacterial stress response and virulence. We also found that Cas2 decreased the survival of M. smegmatis within macrophages. This study provides new insights on the role of Cas2.
成簇规律间隔短回文重复序列(CRISPR)存在于40%的细菌基因组和90%的古细菌基因组中。CRISPR及其相关的Cas蛋白构成了一种针对破坏性移动遗传元件的适应性免疫系统。在结核分枝杆菌基因组中发现了两个CRISPR和9个编码CRISPR相关蛋白的基因。CRISPR相关的Cas2是获取新间隔序列所需的核糖核酸内切酶。在本研究中,由Rv2816c编码的Cas2在缺乏CRISPR-Cas系统的耻垢分枝杆菌中表达,并研究了其在耻垢分枝杆菌体外和巨噬细胞内应激反应中的作用。我们发现,Cas2介导的耻垢分枝杆菌应激反应变化与参与分枝杆菌应激反应和毒力的σ因子表达改变有关。我们还发现,Cas2降低了耻垢分枝杆菌在巨噬细胞内的存活率。本研究为Cas2的作用提供了新的见解。