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Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis

Single-stranded DNA is more subject to mutation than double stranded. During transcription, DNA is transiently single stranded and therefore subject to higher mutagenesis. However, if local intra-strand secondary structures are formed, some bases will be paired and therefore less sensitive to mutati...

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Detalles Bibliográficos
Autores principales: Hoede, Claire, Denamur, Erick, Tenaillon, Olivier
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630709/
https://www.ncbi.nlm.nih.gov/pubmed/17083275
http://dx.doi.org/10.1371/journal.pgen.0020176
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author Hoede, Claire
Denamur, Erick
Tenaillon, Olivier
author_facet Hoede, Claire
Denamur, Erick
Tenaillon, Olivier
author_sort Hoede, Claire
collection PubMed
description Single-stranded DNA is more subject to mutation than double stranded. During transcription, DNA is transiently single stranded and therefore subject to higher mutagenesis. However, if local intra-strand secondary structures are formed, some bases will be paired and therefore less sensitive to mutation than unpaired bases. Using complete genome sequences of Escherichia coli, we show that local intra-strand secondary structures can, as a consequence, be used to define an index of transcription-driven mutability. At gene level, we show that natural selection has favoured a reduced transcription-driven mutagenesis via the higher than expected frequency of occurrence of intra-strand secondary structures. Such selection is stronger in highly expressed genes and suggests a sequence-dependent way to control mutation rates and a novel form of selection affecting the evolution of synonymous mutations.
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spelling pubmed-16307092006-11-29 Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis Hoede, Claire Denamur, Erick Tenaillon, Olivier PLoS Genet Research Article Single-stranded DNA is more subject to mutation than double stranded. During transcription, DNA is transiently single stranded and therefore subject to higher mutagenesis. However, if local intra-strand secondary structures are formed, some bases will be paired and therefore less sensitive to mutation than unpaired bases. Using complete genome sequences of Escherichia coli, we show that local intra-strand secondary structures can, as a consequence, be used to define an index of transcription-driven mutability. At gene level, we show that natural selection has favoured a reduced transcription-driven mutagenesis via the higher than expected frequency of occurrence of intra-strand secondary structures. Such selection is stronger in highly expressed genes and suggests a sequence-dependent way to control mutation rates and a novel form of selection affecting the evolution of synonymous mutations. Public Library of Science 2006-11 2006-11-03 /pmc/articles/PMC1630709/ /pubmed/17083275 http://dx.doi.org/10.1371/journal.pgen.0020176 Text en © 2006 Hoede et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hoede, Claire
Denamur, Erick
Tenaillon, Olivier
Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title_full Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title_fullStr Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title_full_unstemmed Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title_short Selection Acts on DNA Secondary Structures to Decrease Transcriptional Mutagenesis
title_sort selection acts on dna secondary structures to decrease transcriptional mutagenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630709/
https://www.ncbi.nlm.nih.gov/pubmed/17083275
http://dx.doi.org/10.1371/journal.pgen.0020176
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