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The Evolutionary Value of Recombination Is Constrained by Genome Modularity

Genetic recombination is a fundamental evolutionary mechanism promoting biological adaptation. Using engineered recombinants of the small single-stranded DNA plant virus, Maize streak virus (MSV), we experimentally demonstrate that fragments of genetic material only function optimally if they reside...

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Autores principales: Martin, Darren P, van der Walt, Eric, Posada, David, Rybicki, Edward P
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1262190/
https://www.ncbi.nlm.nih.gov/pubmed/16244707
http://dx.doi.org/10.1371/journal.pgen.0010051
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author Martin, Darren P
van der Walt, Eric
Posada, David
Rybicki, Edward P
author_facet Martin, Darren P
van der Walt, Eric
Posada, David
Rybicki, Edward P
author_sort Martin, Darren P
collection PubMed
description Genetic recombination is a fundamental evolutionary mechanism promoting biological adaptation. Using engineered recombinants of the small single-stranded DNA plant virus, Maize streak virus (MSV), we experimentally demonstrate that fragments of genetic material only function optimally if they reside within genomes similar to those in which they evolved. The degree of similarity necessary for optimal functionality is correlated with the complexity of intragenomic interaction networks within which genome fragments must function. There is a striking correlation between our experimental results and the types of MSV recombinants that are detectable in nature, indicating that obligatory maintenance of intragenome interaction networks strongly constrains the evolutionary value of recombination for this virus and probably for genomes in general.
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spelling pubmed-12621902007-02-28 The Evolutionary Value of Recombination Is Constrained by Genome Modularity Martin, Darren P van der Walt, Eric Posada, David Rybicki, Edward P PLoS Genet Research Article Genetic recombination is a fundamental evolutionary mechanism promoting biological adaptation. Using engineered recombinants of the small single-stranded DNA plant virus, Maize streak virus (MSV), we experimentally demonstrate that fragments of genetic material only function optimally if they reside within genomes similar to those in which they evolved. The degree of similarity necessary for optimal functionality is correlated with the complexity of intragenomic interaction networks within which genome fragments must function. There is a striking correlation between our experimental results and the types of MSV recombinants that are detectable in nature, indicating that obligatory maintenance of intragenome interaction networks strongly constrains the evolutionary value of recombination for this virus and probably for genomes in general. Public Library of Science 2005-10 2005-10-21 /pmc/articles/PMC1262190/ /pubmed/16244707 http://dx.doi.org/10.1371/journal.pgen.0010051 Text en Copyright: © 2005 Martin 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
Martin, Darren P
van der Walt, Eric
Posada, David
Rybicki, Edward P
The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title_full The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title_fullStr The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title_full_unstemmed The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title_short The Evolutionary Value of Recombination Is Constrained by Genome Modularity
title_sort evolutionary value of recombination is constrained by genome modularity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1262190/
https://www.ncbi.nlm.nih.gov/pubmed/16244707
http://dx.doi.org/10.1371/journal.pgen.0010051
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