4.7 Article

RNA-activated DNA cleavage by the Type III-B CRISPR-Cas effector complex

期刊

GENES & DEVELOPMENT
卷 30, 期 4, 页码 460-470

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.273722.115

关键词

CRISPR-Cas; CMR; RAMP; nuclease; RNA

资金

  1. National Institutes of Health [GM097330]
  2. Ruth L. Kirschstein National Institutes of Health F31 fellowship [GM105364]

向作者/读者索取更多资源

The CRISPR (clustered regularly interspaced short palindromic repeat) system is an RNA-guided immune system that protects prokaryotes from invading genetic elements. This system represents an inheritable and adaptable immune system that is mediated by multisubunit effector complexes. In the Type III-B system, the Cmr effector complex has been found to cleave ssRNA in vitro. However, in vivo, it has been implicated in transcription-dependent DNA targeting. We show here that the Cmr complex from Thermotoga maritima can cleave an ssRNA target that is complementary to the CRISPR RNA. We also show that binding of a complementary ssRNA target activates an ssDNA-specific nuclease activity in the histidine-aspartate (HD) domain of the Cmr2 subunit of the complex. These data suggest a mechanism for transcription-coupled DNA targeting by the Cmr complex and provide a unifying mechanism for all Type III systems.

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