肠杆菌科 I-E 型和 I-F 型 CRISPR-Cas 系统的机制。

Q1 Medicine
Chaoyou Xue, Dipali G Sashital
{"title":"肠杆菌科 I-E 型和 I-F 型 CRISPR-Cas 系统的机制。","authors":"Chaoyou Xue, Dipali G Sashital","doi":"10.1128/ecosalplus.ESP-0008-2018","DOIUrl":null,"url":null,"abstract":"<p><p>CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against invasion by bacteriophages and other mobile genetic elements. Short fragments of invader DNA are stored as immunological memories within CRISPR (clustered regularly interspaced short palindromic repeat) arrays in the host chromosome. These arrays provide a template for RNA molecules that can guide CRISPR-associated (Cas) proteins to specifically neutralize viruses upon subsequent infection. Over the past 10 years, our understanding of CRISPR-Cas systems has benefited greatly from a number of model organisms. In particular, the study of several members of the Gram-negative <i>Enterobacteriaceae</i> family, especially <i>Escherichia coli</i> and <i>Pectobacterium atrosepticum</i>, have provided significant insights into the mechanisms of CRISPR-Cas immunity. In this review, we provide an overview of CRISPR-Cas systems present in members of the <i>Enterobacteriaceae</i>. We also detail the current mechanistic understanding of the type I-E and type I-F CRISPR-Cas systems that are commonly found in enterobacteria. Finally, we discuss how phages can escape or inactivate CRISPR-Cas systems and the measures bacteria can enact to counter these types of events.</p>","PeriodicalId":11500,"journal":{"name":"EcoSal Plus","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368399/pdf/nihms-1004596.pdf","citationCount":"0","resultStr":"{\"title\":\"Mechanisms of Type I-E and I-F CRISPR-Cas Systems in <i>Enterobacteriaceae</i>.\",\"authors\":\"Chaoyou Xue, Dipali G Sashital\",\"doi\":\"10.1128/ecosalplus.ESP-0008-2018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against invasion by bacteriophages and other mobile genetic elements. Short fragments of invader DNA are stored as immunological memories within CRISPR (clustered regularly interspaced short palindromic repeat) arrays in the host chromosome. These arrays provide a template for RNA molecules that can guide CRISPR-associated (Cas) proteins to specifically neutralize viruses upon subsequent infection. Over the past 10 years, our understanding of CRISPR-Cas systems has benefited greatly from a number of model organisms. In particular, the study of several members of the Gram-negative <i>Enterobacteriaceae</i> family, especially <i>Escherichia coli</i> and <i>Pectobacterium atrosepticum</i>, have provided significant insights into the mechanisms of CRISPR-Cas immunity. In this review, we provide an overview of CRISPR-Cas systems present in members of the <i>Enterobacteriaceae</i>. We also detail the current mechanistic understanding of the type I-E and type I-F CRISPR-Cas systems that are commonly found in enterobacteria. Finally, we discuss how phages can escape or inactivate CRISPR-Cas systems and the measures bacteria can enact to counter these types of events.</p>\",\"PeriodicalId\":11500,\"journal\":{\"name\":\"EcoSal Plus\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368399/pdf/nihms-1004596.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EcoSal Plus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1128/ecosalplus.ESP-0008-2018\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EcoSal Plus","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1128/ecosalplus.ESP-0008-2018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

CRISPR-Cas系统为细菌和古细菌提供适应性免疫力,抵御噬菌体和其他移动遗传因子的入侵。入侵者 DNA 的短片段作为免疫记忆储存在宿主染色体中的 CRISPR(簇状规则间隔短回文重复序列)阵列中。这些阵列为 RNA 分子提供了模板,RNA 分子可以引导 CRISPR 相关(Cas)蛋白在后续感染时特异性地中和病毒。在过去的 10 年中,我们对 CRISPR-Cas 系统的了解极大地得益于一些模式生物。特别是对革兰氏阴性肠杆菌科的几个成员,尤其是大肠杆菌和无核果胶杆菌的研究,为我们深入了解 CRISPR-Cas 免疫机制提供了重要启示。在本综述中,我们概述了肠杆菌科成员中存在的 CRISPR-Cas 系统。我们还详细介绍了目前对肠杆菌中常见的 I-E 型和 I-F 型 CRISPR-Cas 系统的机理认识。最后,我们将讨论噬菌体如何逃避或使 CRISPR-Cas 系统失活,以及细菌可以采取哪些措施来应对这类事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanisms of Type I-E and I-F CRISPR-Cas Systems in <i>Enterobacteriaceae</i>.

Mechanisms of Type I-E and I-F CRISPR-Cas Systems in <i>Enterobacteriaceae</i>.

Mechanisms of Type I-E and I-F CRISPR-Cas Systems in <i>Enterobacteriaceae</i>.

Mechanisms of Type I-E and I-F CRISPR-Cas Systems in Enterobacteriaceae.

CRISPR-Cas systems provide bacteria and archaea with adaptive immunity against invasion by bacteriophages and other mobile genetic elements. Short fragments of invader DNA are stored as immunological memories within CRISPR (clustered regularly interspaced short palindromic repeat) arrays in the host chromosome. These arrays provide a template for RNA molecules that can guide CRISPR-associated (Cas) proteins to specifically neutralize viruses upon subsequent infection. Over the past 10 years, our understanding of CRISPR-Cas systems has benefited greatly from a number of model organisms. In particular, the study of several members of the Gram-negative Enterobacteriaceae family, especially Escherichia coli and Pectobacterium atrosepticum, have provided significant insights into the mechanisms of CRISPR-Cas immunity. In this review, we provide an overview of CRISPR-Cas systems present in members of the Enterobacteriaceae. We also detail the current mechanistic understanding of the type I-E and type I-F CRISPR-Cas systems that are commonly found in enterobacteria. Finally, we discuss how phages can escape or inactivate CRISPR-Cas systems and the measures bacteria can enact to counter these types of events.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
EcoSal Plus
EcoSal Plus Immunology and Microbiology-Microbiology
CiteScore
12.20
自引率
0.00%
发文量
4
期刊介绍: EcoSal Plus is the authoritative online review journal that publishes an ever-growing body of expert reviews covering virtually all aspects of E. coli, Salmonella, and other members of the family Enterobacteriaceae and their use as model microbes for biological explorations. This journal is intended primarily for the research community as a comprehensive and continuously updated archive of the entire corpus of knowledge about the enteric bacterial cell. Thoughtful reviews focus on physiology, metabolism, genetics, pathogenesis, ecology, genomics, systems biology, and history E. coli and its relatives. These provide the integrated background needed for most microbiology investigations and are essential reading for research scientists. Articles contain links to E. coli K12 genes on the EcoCyc database site and are available as downloadable PDF files. Images and tables are downloadable to PowerPoint files.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信