Ichikawa H Travis, Cooper John C, Lo Leja, Potter Jason, Terns Rebecca M, Terns Michael P
Department of Biochemistry and Molecular Biology, University of Georgia, Athens, Georgia, United States of America.
Thermo Fisher Scientific, Carlsbad, California, United States of America.
PLoS One. 2017 Apr 25;12(4):e0176221. doi: 10.1371/journal.pone.0176221. eCollection 2017.
The CRISPR-Cas systems provide invader defense in a wide variety of prokaryotes, as well as technologies for many powerful applications. The Type III-A or Csm CRISPR-Cas system is one of the most widely distributed across prokaryotic phyla, and cleaves targeted DNA and RNA molecules. In this work, we have constructed modules of Csm systems from 3 bacterial species and heterologously expressed the functional modules in E. coli. The modules include a Cas6 protein and a CRISPR locus for crRNA production, and Csm effector complex proteins. The expressed modules from L. lactis, S. epidermidis and S. thermophilus specifically eliminate invading plasmids recognized by the crRNAs of the systems. Characteristically, activation of plasmid targeting activity depends on transcription of the plasmid sequence recognized by the crRNA. Activity was not observed when transcription of the crRNA target sequence was blocked, or when the opposite strand or a non-target sequence was transcribed. Moreover, the Csm module can be programmed to recognize plasmids with novel target sequences by addition of appropriate crRNA coding sequences to the module. These systems provide a platform for investigation of Type III-A CRISPR-Cas systems in E. coli, and for introduction of programmable transcription-activated DNA targeting into novel organisms.
CRISPR-Cas系统为多种原核生物提供抗入侵防御,同时也是许多强大应用技术的基础。III-A型或Csm CRISPR-Cas系统是在原核生物门类中分布最广泛的系统之一,可切割靶向DNA和RNA分子。在本研究中,我们构建了来自3种细菌的Csm系统模块,并在大肠杆菌中进行了异源功能表达。这些模块包括一个Cas6蛋白、一个用于产生crRNA的CRISPR基因座以及Csm效应复合物蛋白。从乳酸乳球菌、表皮葡萄球菌和嗜热栖热菌中表达的模块可特异性消除被系统crRNA识别的入侵质粒。其特点是,质粒靶向活性的激活取决于被crRNA识别的质粒序列的转录。当crRNA靶序列的转录被阻断,或者转录相反链或非靶序列时,未观察到活性。此外,通过向模块中添加适当的crRNA编码序列,可对Csm模块进行编程,使其识别具有新靶序列的质粒。这些系统为在大肠杆菌中研究III-A型CRISPR-Cas系统以及将可编程转录激活DNA靶向引入新生物体提供了一个平台。