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Evolutionary pressures on simple sequence repeats in prokaryotic coding regions
Simple sequence repeats (SSRs) are indel mutational hotspots in genomes. In prokaryotes, SSR loci can cause phase variation, a microbial survival strategy that relies on stochastic, reversible on–off switching of gene activity. By analyzing multiple strains of 42 fully sequenced prokaryotic species,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315296/ https://www.ncbi.nlm.nih.gov/pubmed/22123746 http://dx.doi.org/10.1093/nar/gkr1078 |
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author | Lin, Wei-Hsiang Kussell, Edo |
author_facet | Lin, Wei-Hsiang Kussell, Edo |
author_sort | Lin, Wei-Hsiang |
collection | PubMed |
description | Simple sequence repeats (SSRs) are indel mutational hotspots in genomes. In prokaryotes, SSR loci can cause phase variation, a microbial survival strategy that relies on stochastic, reversible on–off switching of gene activity. By analyzing multiple strains of 42 fully sequenced prokaryotic species, we measure the relative variability and density distribution of SSRs in coding regions. We demonstrate that repeat type strongly influences indel mutation rates, and that the most mutable types are most strongly avoided across genomes. We thoroughly characterize SSR density and variability as a function of N→C position along protein sequences. Using codon-shuffling algorithms that preserve amino acid sequence, we assess evolutionary pressures on SSRs. We find that coding sequences suppress repeats in the middle of proteins, and enrich repeats near termini, yielding U-shaped SSR density curves. We show that for many species this characteristic shape can be attributed to purely biophysical constraints of protein structure. In multiple cases, however, particularly in certain pathogenic bacteria, we observe over enrichment of SSRs near protein N-termini significantly beyond expectation based on structural constraints. This increases the probability that frameshifts result in non-functional proteins, revealing that these species may evolutionarily tune SSR positions in coding regions to facilitate phase variation. |
format | Online Article Text |
id | pubmed-3315296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33152962012-03-30 Evolutionary pressures on simple sequence repeats in prokaryotic coding regions Lin, Wei-Hsiang Kussell, Edo Nucleic Acids Res Computational Biology Simple sequence repeats (SSRs) are indel mutational hotspots in genomes. In prokaryotes, SSR loci can cause phase variation, a microbial survival strategy that relies on stochastic, reversible on–off switching of gene activity. By analyzing multiple strains of 42 fully sequenced prokaryotic species, we measure the relative variability and density distribution of SSRs in coding regions. We demonstrate that repeat type strongly influences indel mutation rates, and that the most mutable types are most strongly avoided across genomes. We thoroughly characterize SSR density and variability as a function of N→C position along protein sequences. Using codon-shuffling algorithms that preserve amino acid sequence, we assess evolutionary pressures on SSRs. We find that coding sequences suppress repeats in the middle of proteins, and enrich repeats near termini, yielding U-shaped SSR density curves. We show that for many species this characteristic shape can be attributed to purely biophysical constraints of protein structure. In multiple cases, however, particularly in certain pathogenic bacteria, we observe over enrichment of SSRs near protein N-termini significantly beyond expectation based on structural constraints. This increases the probability that frameshifts result in non-functional proteins, revealing that these species may evolutionarily tune SSR positions in coding regions to facilitate phase variation. Oxford University Press 2012-03 2011-11-26 /pmc/articles/PMC3315296/ /pubmed/22123746 http://dx.doi.org/10.1093/nar/gkr1078 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Lin, Wei-Hsiang Kussell, Edo Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title | Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title_full | Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title_fullStr | Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title_full_unstemmed | Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title_short | Evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
title_sort | evolutionary pressures on simple sequence repeats in prokaryotic coding regions |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315296/ https://www.ncbi.nlm.nih.gov/pubmed/22123746 http://dx.doi.org/10.1093/nar/gkr1078 |
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