Institute of Evolutionary Biology, University of Edinburgh, The Kings Buildings, West Mains Road, Edinburgh EH9 3JT, UK.
Proc Biol Sci. 2010 Jul 22;277(1691):2097-103. doi: 10.1098/rspb.2010.0055. Epub 2010 Mar 17.
The past is never dead. It's not even past William Faulkner (1951). Bacteria can acquire heritable immunity to viral (phage) enemies by incorporating phage DNA into their own genome. This mechanism of anti-viral defence, known by the acronym CRISPR, simultaneously stores detailed information about current and past enemies and the evolved resistance to them. As a high-resolution genetic marker that is intimately tied with the host-pathogen interaction, the CRISPR system offers a unique, and relatively untapped, opportunity to study epidemiological and coevolutionary dynamics in microbial communities that were previously neglected because they could not be cultured in the laboratory. We briefly review the molecular mechanisms of CRISPR-mediated host-pathogen resistance, before assessing their potential importance for coevolution in nature, and their utility as a means of studying coevolutionary dynamics through metagenomics and laboratory experimentation.
过去从未消逝。正如威廉·福克纳(William Faulkner)所言(1951):“过去永远不会过去。”细菌可以通过将噬菌体 DNA 整合到自身基因组中来获得对病毒(噬菌体)的遗传抗性。这种抗病毒防御机制,简称 CRISPR,同时存储有关当前和过去的敌人以及对它们进化产生的抗性的详细信息。作为一种与宿主-病原体相互作用密切相关的高分辨率遗传标记,CRISPR 系统为研究以前因无法在实验室中培养而被忽视的微生物群落中的流行病学和共同进化动态提供了一个独特且相对未被充分利用的机会。我们简要回顾了 CRISPR 介导的宿主-病原体抗性的分子机制,然后评估了它们在自然界中共同进化的潜在重要性,以及它们作为通过宏基因组学和实验室实验研究共同进化动态的手段的实用性。