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Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery
CRISPR immunity depends on acquisition of fragments of foreign DNA into CRISPR arrays. For type I-E CRISPR–Cas systems two modes of spacer acquisition, naïve and primed adaptation, were described. Naïve adaptation requires just two most conserved Cas1 and Cas2 proteins; it leads to spacer acquisitio...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678832/ https://www.ncbi.nlm.nih.gov/pubmed/26586803 http://dx.doi.org/10.1093/nar/gkv1261 |
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author | Vorontsova, Daria Datsenko, Kirill A. Medvedeva, Sofia Bondy-Denomy, Joseph Savitskaya, Ekaterina E. Pougach, Ksenia Logacheva, Maria Wiedenheft, Blake Davidson, Alan R. Severinov, Konstantin Semenova, Ekaterina |
author_facet | Vorontsova, Daria Datsenko, Kirill A. Medvedeva, Sofia Bondy-Denomy, Joseph Savitskaya, Ekaterina E. Pougach, Ksenia Logacheva, Maria Wiedenheft, Blake Davidson, Alan R. Severinov, Konstantin Semenova, Ekaterina |
author_sort | Vorontsova, Daria |
collection | PubMed |
description | CRISPR immunity depends on acquisition of fragments of foreign DNA into CRISPR arrays. For type I-E CRISPR–Cas systems two modes of spacer acquisition, naïve and primed adaptation, were described. Naïve adaptation requires just two most conserved Cas1 and Cas2 proteins; it leads to spacer acquisition from both foreign and bacterial DNA and results in multiple spacers incapable of immune response. Primed adaptation requires all Cas proteins and a CRISPR RNA recognizing a partially matching target. It leads to selective acquisition of spacers from DNA molecules recognized by priming CRISPR RNA, with most spacers capable of protecting the host. Here, we studied spacer acquisition by a type I-F CRISPR–Cas system. We observe both naïve and primed adaptation. Both processes require not just Cas1 and Cas2, but also intact Csy complex and CRISPR RNA. Primed adaptation shows a gradient of acquisition efficiency as a function of distance from the priming site and a strand bias that is consistent with existence of single-stranded adaption intermediates. The results provide new insights into the mechanism of spacer acquisition and illustrate surprising mechanistic diversity of related CRISPR–Cas systems. |
format | Online Article Text |
id | pubmed-4678832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-46788322015-12-16 Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery Vorontsova, Daria Datsenko, Kirill A. Medvedeva, Sofia Bondy-Denomy, Joseph Savitskaya, Ekaterina E. Pougach, Ksenia Logacheva, Maria Wiedenheft, Blake Davidson, Alan R. Severinov, Konstantin Semenova, Ekaterina Nucleic Acids Res Molecular Biology CRISPR immunity depends on acquisition of fragments of foreign DNA into CRISPR arrays. For type I-E CRISPR–Cas systems two modes of spacer acquisition, naïve and primed adaptation, were described. Naïve adaptation requires just two most conserved Cas1 and Cas2 proteins; it leads to spacer acquisition from both foreign and bacterial DNA and results in multiple spacers incapable of immune response. Primed adaptation requires all Cas proteins and a CRISPR RNA recognizing a partially matching target. It leads to selective acquisition of spacers from DNA molecules recognized by priming CRISPR RNA, with most spacers capable of protecting the host. Here, we studied spacer acquisition by a type I-F CRISPR–Cas system. We observe both naïve and primed adaptation. Both processes require not just Cas1 and Cas2, but also intact Csy complex and CRISPR RNA. Primed adaptation shows a gradient of acquisition efficiency as a function of distance from the priming site and a strand bias that is consistent with existence of single-stranded adaption intermediates. The results provide new insights into the mechanism of spacer acquisition and illustrate surprising mechanistic diversity of related CRISPR–Cas systems. Oxford University Press 2015-12-15 2015-11-19 /pmc/articles/PMC4678832/ /pubmed/26586803 http://dx.doi.org/10.1093/nar/gkv1261 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Vorontsova, Daria Datsenko, Kirill A. Medvedeva, Sofia Bondy-Denomy, Joseph Savitskaya, Ekaterina E. Pougach, Ksenia Logacheva, Maria Wiedenheft, Blake Davidson, Alan R. Severinov, Konstantin Semenova, Ekaterina Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title | Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title_full | Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title_fullStr | Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title_full_unstemmed | Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title_short | Foreign DNA acquisition by the I-F CRISPR–Cas system requires all components of the interference machinery |
title_sort | foreign dna acquisition by the i-f crispr–cas system requires all components of the interference machinery |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678832/ https://www.ncbi.nlm.nih.gov/pubmed/26586803 http://dx.doi.org/10.1093/nar/gkv1261 |
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