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Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective

BACKGROUND: How gene duplication has influenced the evolution of gene networks is one of the core problems in evolution. Current duplication-divergence theories generally suggested that genes on the periphery of the networks were preferentially retained after gene duplication. However, previous stud...

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Autores principales: Huang, Yong, Zheng, Ying, Su, Zhixi, Gu, Xun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709257/
https://www.ncbi.nlm.nih.gov/pubmed/19594873
http://dx.doi.org/10.1186/1471-2164-10-S1-S14
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author Huang, Yong
Zheng, Ying
Su, Zhixi
Gu, Xun
author_facet Huang, Yong
Zheng, Ying
Su, Zhixi
Gu, Xun
author_sort Huang, Yong
collection PubMed
description BACKGROUND: How gene duplication has influenced the evolution of gene networks is one of the core problems in evolution. Current duplication-divergence theories generally suggested that genes on the periphery of the networks were preferentially retained after gene duplication. However, previous studies were mostly based on gene networks in invertebrate species, and they had the inherent shortcoming of not being able to provide information on how the duplication-divergence process proceeded along the time axis during major speciation events. RESULTS: In this study, we constructed a model system consisting of human G protein-coupled receptors (GPCRs) and their downstream genes in the GPCR pathways. These two groups of genes offered a natural partition of genes in the peripheral and the backbone layers of the network. Analysis of the age distributions of the duplication events in human GPCRs and "downstream genes" gene families indicated that they both experienced an explosive expansion at the time of early vertebrate emergence. However, we found only GPCR families saw a continued expansion after early vertebrates, mostly prominently in several small subfamilies of GPCRs involved in immune responses and sensory responses. CONCLUSION: In general, in the human GPCR model system, we found that the position of a gene in the gene networks has significant influences on the likelihood of fixation of its duplicates. However, for a super gene family, the influence was not uniform among subfamilies. For super families, such as GPCRs, whose gene basis of expression diversity was well established at early vertebrates, continued expansions were mostly prominent in particular small subfamilies mainly involved in lineage-specific functions.
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spelling pubmed-27092572009-07-14 Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective Huang, Yong Zheng, Ying Su, Zhixi Gu, Xun BMC Genomics Research BACKGROUND: How gene duplication has influenced the evolution of gene networks is one of the core problems in evolution. Current duplication-divergence theories generally suggested that genes on the periphery of the networks were preferentially retained after gene duplication. However, previous studies were mostly based on gene networks in invertebrate species, and they had the inherent shortcoming of not being able to provide information on how the duplication-divergence process proceeded along the time axis during major speciation events. RESULTS: In this study, we constructed a model system consisting of human G protein-coupled receptors (GPCRs) and their downstream genes in the GPCR pathways. These two groups of genes offered a natural partition of genes in the peripheral and the backbone layers of the network. Analysis of the age distributions of the duplication events in human GPCRs and "downstream genes" gene families indicated that they both experienced an explosive expansion at the time of early vertebrate emergence. However, we found only GPCR families saw a continued expansion after early vertebrates, mostly prominently in several small subfamilies of GPCRs involved in immune responses and sensory responses. CONCLUSION: In general, in the human GPCR model system, we found that the position of a gene in the gene networks has significant influences on the likelihood of fixation of its duplicates. However, for a super gene family, the influence was not uniform among subfamilies. For super families, such as GPCRs, whose gene basis of expression diversity was well established at early vertebrates, continued expansions were mostly prominent in particular small subfamilies mainly involved in lineage-specific functions. BioMed Central 2009-07-07 /pmc/articles/PMC2709257/ /pubmed/19594873 http://dx.doi.org/10.1186/1471-2164-10-S1-S14 Text en Copyright © 2009 Huang 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
Huang, Yong
Zheng, Ying
Su, Zhixi
Gu, Xun
Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title_full Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title_fullStr Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title_full_unstemmed Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title_short Differences in duplication age distributions between human GPCRs and their downstream genes from a network prospective
title_sort differences in duplication age distributions between human gpcrs and their downstream genes from a network prospective
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709257/
https://www.ncbi.nlm.nih.gov/pubmed/19594873
http://dx.doi.org/10.1186/1471-2164-10-S1-S14
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