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CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data
CRISPR arrays and CRISPR-associated (Cas) proteins comprise a widespread adaptive immune system in bacteria and archaea. These systems function as a defense against exogenous parasitic mobile genetic elements that include bacteriophages, plasmids and foreign nucleic acids. With the continuous spread...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671303/ https://www.ncbi.nlm.nih.gov/pubmed/33575613 http://dx.doi.org/10.1093/nargab/lqaa063 |
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author | Podlevsky, Joshua D Hudson, Corey M Timlin, Jerilyn A Williams, Kelly P |
author_facet | Podlevsky, Joshua D Hudson, Corey M Timlin, Jerilyn A Williams, Kelly P |
author_sort | Podlevsky, Joshua D |
collection | PubMed |
description | CRISPR arrays and CRISPR-associated (Cas) proteins comprise a widespread adaptive immune system in bacteria and archaea. These systems function as a defense against exogenous parasitic mobile genetic elements that include bacteriophages, plasmids and foreign nucleic acids. With the continuous spread of antibiotic resistance, knowledge of pathogen susceptibility to bacteriophage therapy is becoming more critical. Additionally, gene-editing applications would benefit from the discovery of new cas genes with favorable properties. While next-generation sequencing has produced staggering quantities of data, transitioning from raw sequencing reads to the identification of CRISPR/Cas systems has remained challenging. This is especially true for metagenomic data, which has the highest potential for identifying novel cas genes. We report a comprehensive computational pipeline, CasCollect, for the targeted assembly and annotation of cas genes and CRISPR arrays—even isolated arrays—from raw sequencing reads. Benchmarking our targeted assembly pipeline demonstrates significantly improved timing by almost two orders of magnitude compared with conventional assembly and annotation, while retaining the ability to detect CRISPR arrays and cas genes. CasCollect is a highly versatile pipeline and can be used for targeted assembly of any specialty gene set, reconfigurable for user provided Hidden Markov Models and/or reference nucleotide sequences. |
format | Online Article Text |
id | pubmed-7671303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76713032021-02-10 CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data Podlevsky, Joshua D Hudson, Corey M Timlin, Jerilyn A Williams, Kelly P NAR Genom Bioinform Standard Article CRISPR arrays and CRISPR-associated (Cas) proteins comprise a widespread adaptive immune system in bacteria and archaea. These systems function as a defense against exogenous parasitic mobile genetic elements that include bacteriophages, plasmids and foreign nucleic acids. With the continuous spread of antibiotic resistance, knowledge of pathogen susceptibility to bacteriophage therapy is becoming more critical. Additionally, gene-editing applications would benefit from the discovery of new cas genes with favorable properties. While next-generation sequencing has produced staggering quantities of data, transitioning from raw sequencing reads to the identification of CRISPR/Cas systems has remained challenging. This is especially true for metagenomic data, which has the highest potential for identifying novel cas genes. We report a comprehensive computational pipeline, CasCollect, for the targeted assembly and annotation of cas genes and CRISPR arrays—even isolated arrays—from raw sequencing reads. Benchmarking our targeted assembly pipeline demonstrates significantly improved timing by almost two orders of magnitude compared with conventional assembly and annotation, while retaining the ability to detect CRISPR arrays and cas genes. CasCollect is a highly versatile pipeline and can be used for targeted assembly of any specialty gene set, reconfigurable for user provided Hidden Markov Models and/or reference nucleotide sequences. Oxford University Press 2020-09-03 /pmc/articles/PMC7671303/ /pubmed/33575613 http://dx.doi.org/10.1093/nargab/lqaa063 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Standard Article Podlevsky, Joshua D Hudson, Corey M Timlin, Jerilyn A Williams, Kelly P CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title | CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title_full | CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title_fullStr | CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title_full_unstemmed | CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title_short | CasCollect: targeted assembly of CRISPR-associated operons from high-throughput sequencing data |
title_sort | cascollect: targeted assembly of crispr-associated operons from high-throughput sequencing data |
topic | Standard Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671303/ https://www.ncbi.nlm.nih.gov/pubmed/33575613 http://dx.doi.org/10.1093/nargab/lqaa063 |
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