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socru: typing of genome-level order and orientation around ribosomal operons in bacteria
Rearrangements of large genome fragments occur in bacteria between repeat sequences and can impact on growth and gene expression. Homologous recombination resulting in inversion between indirect repeats and excision/translocation between direct repeats enables these structural changes. One form of r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478630/ https://www.ncbi.nlm.nih.gov/pubmed/32584752 http://dx.doi.org/10.1099/mgen.0.000396 |
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author | Page, Andrew J. Ainsworth, Emma V. Langridge, Gemma C. |
author_facet | Page, Andrew J. Ainsworth, Emma V. Langridge, Gemma C. |
author_sort | Page, Andrew J. |
collection | PubMed |
description | Rearrangements of large genome fragments occur in bacteria between repeat sequences and can impact on growth and gene expression. Homologous recombination resulting in inversion between indirect repeats and excision/translocation between direct repeats enables these structural changes. One form of rearrangement occurs around ribosomal operons, found in multiple copies across many bacteria, but identification of these rearrangements by sequencing requires reads of several thousand bases to span the ribosomal operons. With long-read sequencing aiding the routine generation of complete bacterial assemblies, we have developed socru, a typing method for the order and orientation of genome fragments between ribosomal operons. It allows for a single identifier to convey the order and orientation of genome-level structure and we have successfully applied this typing to 433 of the most common bacterial species. In a focused analysis, we observed the presence of multiple structural genotypes in nine bacterial pathogens, underscoring the importance of routinely assessing this form of variation alongside traditional single-nucleotide polymorphism (SNP) typing. |
format | Online Article Text |
id | pubmed-7478630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74786302020-09-09 socru: typing of genome-level order and orientation around ribosomal operons in bacteria Page, Andrew J. Ainsworth, Emma V. Langridge, Gemma C. Microb Genom Short Communication Rearrangements of large genome fragments occur in bacteria between repeat sequences and can impact on growth and gene expression. Homologous recombination resulting in inversion between indirect repeats and excision/translocation between direct repeats enables these structural changes. One form of rearrangement occurs around ribosomal operons, found in multiple copies across many bacteria, but identification of these rearrangements by sequencing requires reads of several thousand bases to span the ribosomal operons. With long-read sequencing aiding the routine generation of complete bacterial assemblies, we have developed socru, a typing method for the order and orientation of genome fragments between ribosomal operons. It allows for a single identifier to convey the order and orientation of genome-level structure and we have successfully applied this typing to 433 of the most common bacterial species. In a focused analysis, we observed the presence of multiple structural genotypes in nine bacterial pathogens, underscoring the importance of routinely assessing this form of variation alongside traditional single-nucleotide polymorphism (SNP) typing. Microbiology Society 2020-06-25 /pmc/articles/PMC7478630/ /pubmed/32584752 http://dx.doi.org/10.1099/mgen.0.000396 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Short Communication Page, Andrew J. Ainsworth, Emma V. Langridge, Gemma C. socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title |
socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title_full |
socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title_fullStr |
socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title_full_unstemmed |
socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title_short |
socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
title_sort | socru: typing of genome-level order and orientation around ribosomal operons in bacteria |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478630/ https://www.ncbi.nlm.nih.gov/pubmed/32584752 http://dx.doi.org/10.1099/mgen.0.000396 |
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