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Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation

To acquire the ability to recognize and destroy virus and plasmid invaders, prokaryotic CRISPR–Cas systems capture fragments of DNA within the host CRISPR locus. Our results indicate that the process of adaptation by a Type II-A CRISPR–Cas system in Streptococcus thermophilus requires Cas1, Cas2, an...

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Autores principales: Wei, Yunzhou, Terns, Rebecca M., Terns, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335292/
https://www.ncbi.nlm.nih.gov/pubmed/25691466
http://dx.doi.org/10.1101/gad.257550.114
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author Wei, Yunzhou
Terns, Rebecca M.
Terns, Michael P.
author_facet Wei, Yunzhou
Terns, Rebecca M.
Terns, Michael P.
author_sort Wei, Yunzhou
collection PubMed
description To acquire the ability to recognize and destroy virus and plasmid invaders, prokaryotic CRISPR–Cas systems capture fragments of DNA within the host CRISPR locus. Our results indicate that the process of adaptation by a Type II-A CRISPR–Cas system in Streptococcus thermophilus requires Cas1, Cas2, and Csn2. Surprisingly, we found that Cas9, previously identified as the nuclease responsible for ultimate invader destruction, is also essential for adaptation. Cas9 nuclease activity is dispensable for adaptation. In addition, our studies revealed extensive, unbiased acquisition of the self-targeting host genome sequence by the CRISPR–Cas system that is masked in the presence of active target destruction.
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spelling pubmed-43352922015-08-15 Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation Wei, Yunzhou Terns, Rebecca M. Terns, Michael P. Genes Dev Research Communication To acquire the ability to recognize and destroy virus and plasmid invaders, prokaryotic CRISPR–Cas systems capture fragments of DNA within the host CRISPR locus. Our results indicate that the process of adaptation by a Type II-A CRISPR–Cas system in Streptococcus thermophilus requires Cas1, Cas2, and Csn2. Surprisingly, we found that Cas9, previously identified as the nuclease responsible for ultimate invader destruction, is also essential for adaptation. Cas9 nuclease activity is dispensable for adaptation. In addition, our studies revealed extensive, unbiased acquisition of the self-targeting host genome sequence by the CRISPR–Cas system that is masked in the presence of active target destruction. Cold Spring Harbor Laboratory Press 2015-02-15 /pmc/articles/PMC4335292/ /pubmed/25691466 http://dx.doi.org/10.1101/gad.257550.114 Text en © 2015 Wei et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Communication
Wei, Yunzhou
Terns, Rebecca M.
Terns, Michael P.
Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title_full Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title_fullStr Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title_full_unstemmed Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title_short Cas9 function and host genome sampling in Type II-A CRISPR–Cas adaptation
title_sort cas9 function and host genome sampling in type ii-a crispr–cas adaptation
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335292/
https://www.ncbi.nlm.nih.gov/pubmed/25691466
http://dx.doi.org/10.1101/gad.257550.114
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