Origin and evolution of gene families in Bacteria and Archaea

<p>Abstract</p> <p>Background</p> <p>Comparison of complete genomes of Bacteria and Archaea shows that gene content varies considerably and that genomes evolve quite rapidly via gene duplication and deletion and horizontal gene transfer. We analyze a diverse set of 92 B...

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Main Authors: Merz Hugh, Collins R, Higgs Paul G
Format: Article
Language:English
Published: BMC 2011-10-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/12/S9/S14
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spelling doaj-f97a2988f7234a51ab7f74074a178ad92020-11-24T20:44:30ZengBMCBMC Bioinformatics1471-21052011-10-0112Suppl 9S1410.1186/1471-2105-12-S9-S14Origin and evolution of gene families in Bacteria and ArchaeaMerz HughCollins RHiggs Paul G<p>Abstract</p> <p>Background</p> <p>Comparison of complete genomes of Bacteria and Archaea shows that gene content varies considerably and that genomes evolve quite rapidly via gene duplication and deletion and horizontal gene transfer. We analyze a diverse set of 92 Bacteria and 79 Archaea in order to investigate the processes governing the origin and evolution of families of related genes within genomes.</p> <p>Results</p> <p>Genes were clustered into related groups using similarity criteria derived from BLAST. Most clusters contained genes from only one or a small number of genomes, and relatively few core clusters were found that spanned all genomes. Gene clusters found in larger numbers of genomes tended to have larger numbers of genes per genome; however, clusters with unusually large numbers of genes per genome were found among both narrowly and widely distributed clusters. Larger genomes were found to have larger mean gene family sizes and a greater proportion of families of very large size. We used a model of birth, death, and innovation to predict the distribution of gene family sizes. The key parameter is <it>r</it>, the ratio of duplications to deletions. It was found that the model can give a good fit to the observed distribution only if there are several classes of genes with different values of <it>r.</it> The preferred model in most cases had three classes of genes.</p> <p>Conclusions</p> <p>There appears to be a rapid rate of origination of new gene families within individual genomes. Most of these gene families are deleted before they spread to large numbers of genomes, which suggests that they may not be generally beneficial to the organisms. The family size distribution is best described by a large fraction of families that tend to have only one or two genes and a small fraction of families of multi-copy genes that are highly prone to duplication. Larger families occur more frequently in larger genomes, indicating higher <it>r</it> in these genomes, possibly due to a greater tolerance for non-beneficial gene duplicates. The smallest genomes contain very few multi-copy families, suggesting a high rate of deletion of all but the most beneficial genes in these genomes.</p> http://www.biomedcentral.com/1471-2105/12/S9/S14
collection DOAJ
language English
format Article
sources DOAJ
author Merz Hugh
Collins R
Higgs Paul G
spellingShingle Merz Hugh
Collins R
Higgs Paul G
Origin and evolution of gene families in Bacteria and Archaea
BMC Bioinformatics
author_facet Merz Hugh
Collins R
Higgs Paul G
author_sort Merz Hugh
title Origin and evolution of gene families in Bacteria and Archaea
title_short Origin and evolution of gene families in Bacteria and Archaea
title_full Origin and evolution of gene families in Bacteria and Archaea
title_fullStr Origin and evolution of gene families in Bacteria and Archaea
title_full_unstemmed Origin and evolution of gene families in Bacteria and Archaea
title_sort origin and evolution of gene families in bacteria and archaea
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2011-10-01
description <p>Abstract</p> <p>Background</p> <p>Comparison of complete genomes of Bacteria and Archaea shows that gene content varies considerably and that genomes evolve quite rapidly via gene duplication and deletion and horizontal gene transfer. We analyze a diverse set of 92 Bacteria and 79 Archaea in order to investigate the processes governing the origin and evolution of families of related genes within genomes.</p> <p>Results</p> <p>Genes were clustered into related groups using similarity criteria derived from BLAST. Most clusters contained genes from only one or a small number of genomes, and relatively few core clusters were found that spanned all genomes. Gene clusters found in larger numbers of genomes tended to have larger numbers of genes per genome; however, clusters with unusually large numbers of genes per genome were found among both narrowly and widely distributed clusters. Larger genomes were found to have larger mean gene family sizes and a greater proportion of families of very large size. We used a model of birth, death, and innovation to predict the distribution of gene family sizes. The key parameter is <it>r</it>, the ratio of duplications to deletions. It was found that the model can give a good fit to the observed distribution only if there are several classes of genes with different values of <it>r.</it> The preferred model in most cases had three classes of genes.</p> <p>Conclusions</p> <p>There appears to be a rapid rate of origination of new gene families within individual genomes. Most of these gene families are deleted before they spread to large numbers of genomes, which suggests that they may not be generally beneficial to the organisms. The family size distribution is best described by a large fraction of families that tend to have only one or two genes and a small fraction of families of multi-copy genes that are highly prone to duplication. Larger families occur more frequently in larger genomes, indicating higher <it>r</it> in these genomes, possibly due to a greater tolerance for non-beneficial gene duplicates. The smallest genomes contain very few multi-copy families, suggesting a high rate of deletion of all but the most beneficial genes in these genomes.</p>
url http://www.biomedcentral.com/1471-2105/12/S9/S14
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