Department of Clinical Microbiology and Immunology, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Department of Regulation in Infection Biology, Helmholtz Centre for Infection Research, Braunschweig 38124, Germany; Department of Regulation in Infection Biology, Max Planck Institute for Infection Biology, Berlin 10117, Germany.
Mol Cell. 2016 Mar 17;61(6):797-808. doi: 10.1016/j.molcel.2016.01.030. Epub 2016 Mar 3.
Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins constitute an adaptive immune system in prokaryotes. The system preserves memories of prior infections by integrating short segments of foreign DNA, termed spacers, into the CRISPR array in a process termed adaptation. During the past 3 years, significant progress has been made on the genetic requirements and molecular mechanisms of adaptation. Here we review these recent advances, with a focus on the experimental approaches that have been developed, the insights they generated, and a proposed mechanism for self- versus non-self-discrimination during the process of spacer selection. We further describe the regulation of adaptation and the protein players involved in this fascinating process that allows bacteria and archaea to harbor adaptive immunity.
成簇规律间隔短回文重复序列 (CRISPR) 和 CRISPR 相关 (Cas) 蛋白构成了原核生物的适应性免疫系统。该系统通过将称为间隔区的外源 DNA 短片段整合到 CRISPR 阵列中,从而对先前的感染产生记忆,这个过程称为适应。在过去的 3 年中,人们在适应的遗传要求和分子机制方面取得了重大进展。在这里,我们回顾这些最新进展,重点介绍已开发的实验方法、它们所产生的见解,以及在间隔区选择过程中自我与非自我区分的建议机制。我们还进一步描述了适应的调控以及该迷人过程中涉及的蛋白,该过程使细菌和古菌能够拥有适应性免疫。