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The human phylome

BACKGROUND: Phylogenomics analyses serve to establish evolutionary relationships among organisms and their genes. A phylome, the complete collection of all gene phylogenies in a genome, constitutes a valuable source of information, but its use in large genomes still constitutes a technical challenge...

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Autores principales: Huerta-Cepas, Jaime, Dopazo, Hernán, Dopazo, Joaquín, Gabaldón, Toni
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394744/
https://www.ncbi.nlm.nih.gov/pubmed/17567924
http://dx.doi.org/10.1186/gb-2007-8-6-r109
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author Huerta-Cepas, Jaime
Dopazo, Hernán
Dopazo, Joaquín
Gabaldón, Toni
author_facet Huerta-Cepas, Jaime
Dopazo, Hernán
Dopazo, Joaquín
Gabaldón, Toni
author_sort Huerta-Cepas, Jaime
collection PubMed
description BACKGROUND: Phylogenomics analyses serve to establish evolutionary relationships among organisms and their genes. A phylome, the complete collection of all gene phylogenies in a genome, constitutes a valuable source of information, but its use in large genomes still constitutes a technical challenge. The use of phylomes also requires the development of new methods that help us to interpret them. RESULTS: We reconstruct here the human phylome, which includes the evolutionary relationships of all human proteins and their homologs among 39 fully sequenced eukaryotes. Phylogenetic techniques used include alignment trimming, branch length optimization, evolutionary model testing and maximum likelihood and Bayesian methods. Although differences with alternative topologies are minor, most of the trees support the Coelomata and Unikont hypotheses as well as the grouping of primates with laurasatheria to the exclusion of rodents. We assess the extent of gene duplication events and their relationship with the functional roles of the protein families involved. We find support for at least one, and probably two, rounds of whole genome duplications before vertebrate radiation. Using a novel algorithm that is independent from a species phylogeny, we derive orthology and paralogy relationships of human proteins among eukaryotic genomes. CONCLUSION: Topological variations among phylogenies for different genes are to be expected, highlighting the danger of gene-sampling effects in phylogenomic analyses. Several links can be established between the functions of gene families duplicated at certain phylogenetic splits and major evolutionary transitions in those lineages. The pipeline implemented here can be easily adapted for use in other organisms.
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spelling pubmed-23947442008-05-24 The human phylome Huerta-Cepas, Jaime Dopazo, Hernán Dopazo, Joaquín Gabaldón, Toni Genome Biol Research BACKGROUND: Phylogenomics analyses serve to establish evolutionary relationships among organisms and their genes. A phylome, the complete collection of all gene phylogenies in a genome, constitutes a valuable source of information, but its use in large genomes still constitutes a technical challenge. The use of phylomes also requires the development of new methods that help us to interpret them. RESULTS: We reconstruct here the human phylome, which includes the evolutionary relationships of all human proteins and their homologs among 39 fully sequenced eukaryotes. Phylogenetic techniques used include alignment trimming, branch length optimization, evolutionary model testing and maximum likelihood and Bayesian methods. Although differences with alternative topologies are minor, most of the trees support the Coelomata and Unikont hypotheses as well as the grouping of primates with laurasatheria to the exclusion of rodents. We assess the extent of gene duplication events and their relationship with the functional roles of the protein families involved. We find support for at least one, and probably two, rounds of whole genome duplications before vertebrate radiation. Using a novel algorithm that is independent from a species phylogeny, we derive orthology and paralogy relationships of human proteins among eukaryotic genomes. CONCLUSION: Topological variations among phylogenies for different genes are to be expected, highlighting the danger of gene-sampling effects in phylogenomic analyses. Several links can be established between the functions of gene families duplicated at certain phylogenetic splits and major evolutionary transitions in those lineages. The pipeline implemented here can be easily adapted for use in other organisms. BioMed Central 2007 2007-06-13 /pmc/articles/PMC2394744/ /pubmed/17567924 http://dx.doi.org/10.1186/gb-2007-8-6-r109 Text en Copyright © 2007 Huerta-Cepas, et al.; 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
Huerta-Cepas, Jaime
Dopazo, Hernán
Dopazo, Joaquín
Gabaldón, Toni
The human phylome
title The human phylome
title_full The human phylome
title_fullStr The human phylome
title_full_unstemmed The human phylome
title_short The human phylome
title_sort human phylome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394744/
https://www.ncbi.nlm.nih.gov/pubmed/17567924
http://dx.doi.org/10.1186/gb-2007-8-6-r109
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