New faces of prokaryotic mobile genetic elements: Guide RNAs link transposition with host defense mechanisms

被引:5
|
作者
Koonin, Eugene V. [1 ]
Krupovic, Mart [2 ]
机构
[1] Natl Lib Med, Natl Ctr Biotechnol Informat, Bethesda, MD 20894 USA
[2] Univ Paris Cite, Inst Pasteur, Archaeal Virol Unit, CNRS UMR6047, 25 Rue Dr Roux, F-75015 Paris, France
基金
美国国家卫生研究院;
关键词
CRISPR-CAS SYSTEMS; STRUCTURAL BASIS; EVOLUTION; DIVERSITY; TN7; CLASSIFICATION; TRANSPOSASES; GENOMICS;
D O I
10.1016/j.coisb.2023.100473
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Most life forms harbor multiple, diverse mobile genetic elements (MGE) that widely differ in their rates and mechanisms of mobility. Recent findings on two classes of MGE in prokaryotes revealed a novel mechanism, RNA-guided transposition, where a transposon-encoded guide RNA directs the transposase to a unique site in the host genome. Tn7-like transposons, on multiple occasions, recruited CRISPR systems that lost the capacity to cleave target DNA and instead mediate RNA-guided transposition via CRISPR RNA. Conversely, the abundant transposon-associated, RNA-guided nucleases IscB and TnpB that appear to promote proliferation of IS200/IS605 and IS607 transposons were the likely evolutionary ancestors of type II and type V CRISPR systems, respectively. Thus, RNA-guided target recognition is a major biological phenomenon that connects MGE with host defense mechanisms. More RNA-guided defensive and MGE-associated functionalities are likely to be discovered.
引用
收藏
页数:11
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