Charpentier Emmanuelle, Richter Hagen, van der Oost John, White Malcolm F
Helmholtz Centre for Infection Research, Department of Regulation in Infection Biology, Braunschweig 38124, Germany The Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå Centre for Microbial Research (UCMR), Department of Molecular Biology, Umeå University, Umeå 90187, Sweden Hannover Medical School, Hannover 30625, Germany
Helmholtz Centre for Infection Research, Department of Regulation in Infection Biology, Braunschweig 38124, Germany.
FEMS Microbiol Rev. 2015 May;39(3):428-41. doi: 10.1093/femsre/fuv023. Epub 2015 May 19.
CRISPR-Cas is an RNA-mediated adaptive immune system that defends bacteria and archaea against mobile genetic elements. Short mature CRISPR RNAs (crRNAs) are key elements in the interference step of the immune pathway. A CRISPR array composed of a series of repeats interspaced by spacer sequences acquired from invading mobile genomes is transcribed as a precursor crRNA (pre-crRNA) molecule. This pre-crRNA undergoes one or two maturation steps to generate the mature crRNAs that guide CRISPR-associated (Cas) protein(s) to cognate invading genomes for their destruction. Different types of CRISPR-Cas systems have evolved distinct crRNA biogenesis pathways that implicate highly sophisticated processing mechanisms. In Types I and III CRISPR-Cas systems, a specific endoribonuclease of the Cas6 family, either standalone or in a complex with other Cas proteins, cleaves the pre-crRNA within the repeat regions. In Type II systems, the trans-acting small RNA (tracrRNA) base pairs with each repeat of the pre-crRNA to form a dual-RNA that is cleaved by the housekeeping RNase III in the presence of the protein Cas9. In this review, we present a detailed comparative analysis of pre-crRNA recognition and cleavage mechanisms involved in the biogenesis of guide crRNAs in the three CRISPR-Cas types.
CRISPR-Cas是一种RNA介导的适应性免疫系统,可保护细菌和古细菌免受移动遗传元件的侵害。短的成熟CRISPR RNA(crRNA)是免疫途径干扰步骤中的关键元件。由一系列重复序列间隔排列的CRISPR阵列,这些重复序列由从入侵的移动基因组中获取的间隔序列隔开,被转录为前体crRNA(pre-crRNA)分子。这种pre-crRNA经过一个或两个成熟步骤,生成成熟的crRNA,引导CRISPR相关(Cas)蛋白识别并破坏同源入侵基因组。不同类型的CRISPR-Cas系统进化出了不同的crRNA生物合成途径,这些途径涉及高度复杂的加工机制。在I型和III型CRISPR-Cas系统中,Cas6家族的特定核糖核酸内切酶,无论是单独存在还是与其他Cas蛋白形成复合物,都会在重复区域内切割pre-crRNA。在II型系统中,反式作用小RNA(tracrRNA)与pre-crRNA的每个重复序列碱基配对,形成双链RNA,在Cas9蛋白存在的情况下,由管家核糖核酸酶III切割。在这篇综述中,我们对三种CRISPR-Cas类型中引导crRNA生物合成过程中涉及的pre-crRNA识别和切割机制进行了详细的比较分析。