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Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont

Indel mutations play key roles in genome and protein evolution, yet we lack a comprehensive understanding of how indels impact evolutionary processes. Genome-wide analyses enabled by next-generation sequencing can clarify the context and effect of indels, thereby integrating a more detailed consider...

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Autores principales: Williams, Laura E., Wernegreen, Jennifer J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622351/
https://www.ncbi.nlm.nih.gov/pubmed/23475937
http://dx.doi.org/10.1093/gbe/evt033
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author Williams, Laura E.
Wernegreen, Jennifer J.
author_facet Williams, Laura E.
Wernegreen, Jennifer J.
author_sort Williams, Laura E.
collection PubMed
description Indel mutations play key roles in genome and protein evolution, yet we lack a comprehensive understanding of how indels impact evolutionary processes. Genome-wide analyses enabled by next-generation sequencing can clarify the context and effect of indels, thereby integrating a more detailed consideration of indels with our knowledge of nucleotide substitutions. To this end, we sequenced Blochmannia chromaiodes, an obligate bacterial endosymbiont of carpenter ants, and compared it with the close relative, B. pennsylvanicus. The genetic distance between these species is small enough for accurate whole genome alignment but large enough to provide a meaningful spectrum of indel mutations. We found that indels are subjected to purifying selection in coding regions and even intergenic regions, which show a reduced rate of indel base pairs per kilobase compared with nonfunctional pseudogenes. Indels occur almost exclusively in repeat regions composed of homopolymers and multimeric simple sequence repeats, demonstrating the importance of sequence context for indel mutations. Despite purifying selection, some indels occur in protein-coding genes. Most are multiples of three, indicating selective pressure to maintain the reading frame. The deleterious effect of frameshift-inducing indels is minimized by either compensation from a nearby indel to restore reading frame or the indel’s location near the 3'-end of the gene. We observed amino acid divergence exceeding nucleotide divergence in regions affected by frameshift-inducing indels, suggesting that these indels may either drive adaptive protein evolution or initiate gene degradation. Our results shed light on how indel mutations impact processes of molecular evolution underlying endosymbiont genome evolution.
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spelling pubmed-36223512013-04-10 Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont Williams, Laura E. Wernegreen, Jennifer J. Genome Biol Evol Letter Indel mutations play key roles in genome and protein evolution, yet we lack a comprehensive understanding of how indels impact evolutionary processes. Genome-wide analyses enabled by next-generation sequencing can clarify the context and effect of indels, thereby integrating a more detailed consideration of indels with our knowledge of nucleotide substitutions. To this end, we sequenced Blochmannia chromaiodes, an obligate bacterial endosymbiont of carpenter ants, and compared it with the close relative, B. pennsylvanicus. The genetic distance between these species is small enough for accurate whole genome alignment but large enough to provide a meaningful spectrum of indel mutations. We found that indels are subjected to purifying selection in coding regions and even intergenic regions, which show a reduced rate of indel base pairs per kilobase compared with nonfunctional pseudogenes. Indels occur almost exclusively in repeat regions composed of homopolymers and multimeric simple sequence repeats, demonstrating the importance of sequence context for indel mutations. Despite purifying selection, some indels occur in protein-coding genes. Most are multiples of three, indicating selective pressure to maintain the reading frame. The deleterious effect of frameshift-inducing indels is minimized by either compensation from a nearby indel to restore reading frame or the indel’s location near the 3'-end of the gene. We observed amino acid divergence exceeding nucleotide divergence in regions affected by frameshift-inducing indels, suggesting that these indels may either drive adaptive protein evolution or initiate gene degradation. Our results shed light on how indel mutations impact processes of molecular evolution underlying endosymbiont genome evolution. Oxford University Press 2013 2013-03-07 /pmc/articles/PMC3622351/ /pubmed/23475937 http://dx.doi.org/10.1093/gbe/evt033 Text en © The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 Letter
Williams, Laura E.
Wernegreen, Jennifer J.
Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title_full Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title_fullStr Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title_full_unstemmed Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title_short Sequence Context of Indel Mutations and Their Effect on Protein Evolution in a Bacterial Endosymbiont
title_sort sequence context of indel mutations and their effect on protein evolution in a bacterial endosymbiont
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622351/
https://www.ncbi.nlm.nih.gov/pubmed/23475937
http://dx.doi.org/10.1093/gbe/evt033
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