Brouns Stan J J, Jore Matthijs M, Lundgren Magnus, Westra Edze R, Slijkhuis Rik J H, Snijders Ambrosius P L, Dickman Mark J, Makarova Kira S, Koonin Eugene V, van der Oost John
Laboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University, Dreijenplein 10, 6703 HB Wageningen, Netherlands.
Science. 2008 Aug 15;321(5891):960-4. doi: 10.1126/science.1159689.
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.
原核生物通过将病毒核酸的短片段整合到成簇规律间隔短回文重复序列(CRISPRs)中来获得病毒抗性。在这里,我们展示了宿主的CRISPR相关(Cas)蛋白如何利用CRISPRs中包含的病毒衍生序列来介导一种抗病毒反应,以对抗感染。CRISPR转录后,一种称为Cascade的Cas蛋白复合物在每个重复序列中切割CRISPR RNA前体,并保留含有病毒衍生序列的切割产物。在解旋酶Cas3的协助下,这些成熟的CRISPR RNA随后作为小向导RNA,使Cascade能够干扰病毒增殖。我们的结果表明,Cascade的CRISPR RNA内切核酸酶亚基形成成熟向导RNA是抗病毒防御的一个机制要求。