Co-transcriptional DNA and RNA Cleavage during Type III CRISPR-Cas Immunity
Immune systems must recognize and destroy different pathogens that threaten the host. CRISPR-Cas immune systems protect prokaryotes from viral and plasmid infection utilizing small CRISPR RNAs that are complementary to the invader’s genome and specify the targets of RNA-guided Cas nucleases. Type II...
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Published in | Cell Vol. 161; no. 5; pp. 1164 - 1174 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
21.05.2015
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Subjects | |
Online Access | Get full text |
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Summary: | Immune systems must recognize and destroy different pathogens that threaten the host. CRISPR-Cas immune systems protect prokaryotes from viral and plasmid infection utilizing small CRISPR RNAs that are complementary to the invader’s genome and specify the targets of RNA-guided Cas nucleases. Type III CRISPR-Cas immunity requires target transcription, and whereas genetic studies demonstrated DNA targeting, in vitro data have shown crRNA-guided RNA cleavage. The molecular mechanism behind these disparate activities is not known. Here, we show that transcription across the targets of the Staphylococcus epidermidis type III-A CRISPR-Cas system results in the cleavage of the target DNA and its transcripts, mediated by independent active sites within the Cas10-Csm ribonucleoprotein effector complex. Immunity against plasmids and DNA viruses requires DNA, but not RNA, cleavage activity. Our studies reveal a highly versatile mechanism of CRISPR immunity that can defend microorganisms against diverse DNA and RNA invaders.
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•Type III CRISPR-Cas systems provide immunity when the target DNA is transcribed•The type III Cas10-Csm complex performs co-transcriptional RNA-guided DNA cleavage•The complex is also capable of RNA-guided RNA cleavage•Both the target DNA and its transcript are subject to RNA-guided cleavage in vivo
The type III-A CRISPR-Cas system is capable of RNA-guided DNA and RNA cleavage in vivo, revealing a highly versatile mechanism of CRISPR immunity that protects microorganisms against diverse DNA and RNA invaders. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: Department of Biological Sciences, The University of Alabama, 300 Hackberry Lane, Tuscaloosa, AL 35487, USA. |
ISSN: | 0092-8674 1097-4172 1097-4172 |
DOI: | 10.1016/j.cell.2015.04.027 |