Yu Zhenxiao, Jiang Suping, Wang Yuan, Tian Xuhui, Zhao Pengpeng, Xu Jianan, Feng Mingxia, She Qunxin
CRISPR and Archaea Biology Research Center, State Key Laboratory of Microbial Technology, Shandong University, Qingdao, 266237, China.
State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, 430070, China.
Sci China Life Sci. 2021 May;64(5):678-696. doi: 10.1007/s11427-020-1745-0. Epub 2020 Oct 29.
CRISPR-Cas systems provide the small RNA-based adaptive immunity to defend against invasive genetic elements in archaea and bacteria. Organisms of Sulfolobales, an order of thermophilic acidophiles belonging to the Crenarchaeotal Phylum, usually contain both type I and type III CRISPR-Cas systems. Two species, Saccharolobus solfataricus and Sulfolobus islandicus, have been important models for CRISPR study in archaea, and knowledge obtained from these studies has greatly expanded our understanding of molecular mechanisms of antiviral defense in all three steps: adaptation, expression and crRNA processing, and interference. Four subtypes of CRISPR-Cas systems are common in these organisms, including I-A, I-D, III-B, and III-D. These cas genes form functional modules, e.g., all genes required for adaptation and for interference in the I-A immune system are clustered together to form aCas and iCas modules. Genetic assays have been developed to study mechanisms of adaptation and interference by different CRISPR-Cas systems in these model archaea, and these methodologies are useful in demonstration of the protospacer-adjacent motif (PAM)-dependent DNA interference by I-A interference modules and multiple interference activities by III-B Cmr systems. Ribonucleoprotein effector complexes have been isolated for Sulfolobales III-B and III-D systems, and their biochemical characterization has greatly enriched the knowledge of molecular mechanisms of these novel antiviral immune responses.
CRISPR-Cas系统提供基于小RNA的适应性免疫,以抵御古菌和细菌中的入侵遗传元件。硫化叶菌目(属于泉古菌门的嗜热嗜酸菌目)的生物体通常同时含有I型和III型CRISPR-Cas系统。嗜热栖热菌和冰岛硫化叶菌这两个物种一直是古菌中CRISPR研究的重要模型,从这些研究中获得的知识极大地扩展了我们对抗病毒防御分子机制在适应、表达和crRNA加工以及干扰这三个步骤的理解。CRISPR-Cas系统的四种亚型在这些生物体中很常见,包括I-A、I-D、III-B和III-D。这些cas基因形成功能模块,例如,I-A免疫系统中适应和干扰所需的所有基因聚集在一起形成aCas和iCas模块。已经开发了遗传检测方法来研究这些模型古菌中不同CRISPR-Cas系统的适应和干扰机制,这些方法有助于证明I-A干扰模块的原间隔序列相邻基序(PAM)依赖性DNA干扰以及III-B Cmr系统的多种干扰活性。已经分离出了硫化叶菌目III-B和III-D系统的核糖核蛋白效应复合物,它们的生化特性极大地丰富了这些新型抗病毒免疫反应分子机制的知识。