清脆的
反式激活crRNA
生物
核糖核酸
CRISPR干扰
引导RNA
解旋酶
遗传学
抄写(语言学)
核酸内切酶
核酸
Cas9
回文
DNA
病毒
计算生物学
病毒学
细胞生物学
基因
语言学
哲学
作者
Stan J. J. Brouns,Matthijs M. Jore,Magnus Lundgren,Edze R. Westra,Rik J. H. Slijkhuis,Ambrosius P. Snijders,Mark J. Dickman,Kira S. Makarova,Eugene V. Koonin,John van der Oost
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2008-08-14
卷期号:321 (5891): 960-964
被引量:2455
标识
DOI:10.1126/science.1159689
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.
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