Small CRISPR RNAs guide antiviral defense in prokaryotes

被引:1857
作者
Brouns, Stan J. J. [1 ]
Jore, Matthijs M. [1 ]
Lundgren, Magnus [1 ]
Westra, Edze R. [1 ]
Slijkhuis, Rik J. H. [1 ]
Snijders, Ambrosius P. L. [2 ]
Dickman, Mark J. [2 ]
Makarova, Kira S. [3 ]
Koonin, Eugene V. [3 ]
van der Oost, John [1 ]
机构
[1] Univ Wageningen & Res Ctr, Dept Agrotechnol & Food Sci, Microbiol Lab, NL-6703 HB Wageningen, Netherlands
[2] Univ Sheffield, Dept Chem & Proc Engn, Sheffield S1 3JD, S Yorkshire, England
[3] NIH, Natl Ctr Biotechnol Informat, Natl Lib Med, Bethesda, MD 20894 USA
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1126/science.1159689
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prokaryotes acquire virus resistance by integrating short fragments of viral nucleic acid into clusters of regularly interspaced short palindromic repeats ( CRISPRs). Here we show how virus- derived sequences contained in CRISPRs are used by CRISPR- associated ( Cas) proteins from the host to mediate an antiviral response that counteracts infection. After transcription of the CRISPR, a complex of Cas proteins termed Cascade cleaves a CRISPR RNA precursor in each repeat and retains the cleavage products containing the virus- derived sequence. Assisted by the helicase Cas3, these mature CRISPR RNAs then serve as small guide RNAs that enable Cascade to interfere with virus proliferation. Our results demonstrate that the formation of mature guide RNAs by the CRISPR RNA endonuclease subunit of Cascade is a mechanistic requirement for antiviral defense.
引用
收藏
页码:960 / 964
页数:5
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