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Site specific rates of mitochondrial genomes and the phylogeny of eutheria
BACKGROUND: Traditionally, most studies employing data from whole mitochondrial genomes to diagnose relationships among the major lineages of mammals have attempted to exclude regions that potentially complicate phylogenetic analysis. Components generally excluded are 3(rd )codon positions of protei...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796853/ https://www.ncbi.nlm.nih.gov/pubmed/17254354 http://dx.doi.org/10.1186/1471-2148-7-8 |
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author | Kjer, Karl M Honeycutt, Rodney L |
author_facet | Kjer, Karl M Honeycutt, Rodney L |
author_sort | Kjer, Karl M |
collection | PubMed |
description | BACKGROUND: Traditionally, most studies employing data from whole mitochondrial genomes to diagnose relationships among the major lineages of mammals have attempted to exclude regions that potentially complicate phylogenetic analysis. Components generally excluded are 3(rd )codon positions of protein-encoding genes, the control region, rRNAs, tRNAs, and the ND6 gene (encoded on the opposite strand). We present an approach that includes all the data, with the exception of the control region. This approach is based on a site-specific rate model that accommodates excessive homoplasy and that utilizes secondary structure as a reference for proper alignment of rRNAs and tRNAs. RESULTS: Mitochondrial genomic data for 78 eutherian mammals, 8 metatherians, and 3 monotremes were analyzed with a Bayesian analysis and our site specific rate model. The resultant phylogeny revealed strong support for most nodes and was highly congruent with more recent phylogenies based on nuclear DNA sequences. In addition, many of the conflicting relationships observed by earlier mitochondrial-based analyses were resolved without need for the exclusion of large subsets of the data. CONCLUSION: Rather than exclusion of data to minimize presumed noise associated with non-protein encoding genes in the mitochondrial genome, our results indicate that selection of an appropriate model that accommodates rate heterogeneity across data partitions and proper treatment of RNA genes can result in a mitochondrial genome-based phylogeny of eutherian mammals that is reasonably congruent with recent phylogenies derived from nuclear genes. |
format | Text |
id | pubmed-1796853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-17968532007-02-10 Site specific rates of mitochondrial genomes and the phylogeny of eutheria Kjer, Karl M Honeycutt, Rodney L BMC Evol Biol Research Article BACKGROUND: Traditionally, most studies employing data from whole mitochondrial genomes to diagnose relationships among the major lineages of mammals have attempted to exclude regions that potentially complicate phylogenetic analysis. Components generally excluded are 3(rd )codon positions of protein-encoding genes, the control region, rRNAs, tRNAs, and the ND6 gene (encoded on the opposite strand). We present an approach that includes all the data, with the exception of the control region. This approach is based on a site-specific rate model that accommodates excessive homoplasy and that utilizes secondary structure as a reference for proper alignment of rRNAs and tRNAs. RESULTS: Mitochondrial genomic data for 78 eutherian mammals, 8 metatherians, and 3 monotremes were analyzed with a Bayesian analysis and our site specific rate model. The resultant phylogeny revealed strong support for most nodes and was highly congruent with more recent phylogenies based on nuclear DNA sequences. In addition, many of the conflicting relationships observed by earlier mitochondrial-based analyses were resolved without need for the exclusion of large subsets of the data. CONCLUSION: Rather than exclusion of data to minimize presumed noise associated with non-protein encoding genes in the mitochondrial genome, our results indicate that selection of an appropriate model that accommodates rate heterogeneity across data partitions and proper treatment of RNA genes can result in a mitochondrial genome-based phylogeny of eutherian mammals that is reasonably congruent with recent phylogenies derived from nuclear genes. BioMed Central 2007-01-25 /pmc/articles/PMC1796853/ /pubmed/17254354 http://dx.doi.org/10.1186/1471-2148-7-8 Text en Copyright © 2007 Kjer and Honeycutt; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kjer, Karl M Honeycutt, Rodney L Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title | Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title_full | Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title_fullStr | Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title_full_unstemmed | Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title_short | Site specific rates of mitochondrial genomes and the phylogeny of eutheria |
title_sort | site specific rates of mitochondrial genomes and the phylogeny of eutheria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796853/ https://www.ncbi.nlm.nih.gov/pubmed/17254354 http://dx.doi.org/10.1186/1471-2148-7-8 |
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