Suppr超能文献

II-A型CRISPR前导区域中的保守DNA基序。

Conserved DNA motifs in the type II-A CRISPR leader region.

作者信息

Van Orden Mason J, Klein Peter, Babu Kesavan, Najar Fares Z, Rajan Rakhi

机构信息

Department of Chemistry and Biochemistry, University of Oklahoma, Norman, OK, USA.

出版信息

PeerJ. 2017 Apr 4;5:e3161. doi: 10.7717/peerj.3161. eCollection 2017.

Abstract

The Clustered Regularly Interspaced Short Palindromic Repeats associated (CRISPR-Cas) systems consist of RNA-protein complexes that provide bacteria and archaea with sequence-specific immunity against bacteriophages, plasmids, and other mobile genetic elements. Bacteria and archaea become immune to phage or plasmid infections by inserting short pieces of the intruder DNA (spacer) site-specifically into the leader-repeat junction in a process called adaptation. Previous studies have shown that parts of the leader region, especially the 3' end of the leader, are indispensable for adaptation. However, a comprehensive analysis of leader ends remains absent. Here, we have analyzed the leader, repeat, and Cas proteins from 167 type II-A CRISPR loci. Our results indicate two distinct conserved DNA motifs at the 3' leader end: ATTTGAG (noted previously in the CRISPR1 locus of DGCC7710) and a newly defined CTRCGAG, associated with the CRISPR3 locus of DGCC7710. A third group with a very short CG DNA conservation at the 3' leader end is observed mostly in lactobacilli. Analysis of the repeats and Cas proteins revealed clustering of these CRISPR components that mirrors the leader motif clustering, in agreement with the coevolution of CRISPR-Cas components. Based on our analysis of the type II-A CRISPR loci, we implicate leader end sequences that could confer site-specificity for the adaptation-machinery in the different subsets of type II-A CRISPR loci.

摘要

成簇规律间隔短回文重复序列相关(CRISPR-Cas)系统由RNA-蛋白质复合物组成,该复合物为细菌和古细菌提供针对噬菌体、质粒和其他移动遗传元件的序列特异性免疫。细菌和古细菌通过在一个称为适应的过程中,将入侵者DNA的短片段(间隔序列)位点特异性地插入前导序列-重复序列连接处,从而对噬菌体或质粒感染产生免疫。先前的研究表明,前导序列区域的部分,特别是前导序列的3'端,对于适应过程是必不可少的。然而,目前仍缺乏对前导序列末端的全面分析。在此,我们分析了来自167个II-A型CRISPR基因座的前导序列、重复序列和Cas蛋白。我们的结果表明,在3'前导序列末端存在两个不同的保守DNA基序:ATTTGAG(先前在DGCC7710的CRISPR1基因座中被提及)以及一个新定义的CTRCGAG,它与DGCC则7710的CRISPR3基因座相关。在3'前导序列末端具有非常短的CG DNA保守性的第三组主要在乳酸杆菌中观察到。对重复序列和Cas蛋白的分析揭示了这些CRISPR组件的聚类,这反映了前导基序聚类,这与CRISPR-Cas组件的共同进化一致。基于我们对II-A型CRISPR基因座的分析,我们发现了前导序列末端序列,这些序列可能赋予II-A型CRISPR基因座不同亚组中适应机制的位点特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9231/5382924/2bedfd8a25dc/peerj-05-3161-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验