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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
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.
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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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