Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.

<h4>Background</h4>The myocyte enhancer factor 2 (MEF2) gene family is broadly expressed during the development and maintenance of muscle cells. Although a great deal has been elucidated concerning MEF2 transcription factors' regulation of specific gene expression in diverse program...

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Main Authors: Wenwu Wu, Stefan de Folter, Xia Shen, Wenqian Zhang, Shiheng Tao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-03-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21394201/pdf/?tool=EBI
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author Wenwu Wu
Stefan de Folter
Xia Shen
Wenqian Zhang
Shiheng Tao
author_facet Wenwu Wu
Stefan de Folter
Xia Shen
Wenqian Zhang
Shiheng Tao
author_sort Wenwu Wu
collection DOAJ
description <h4>Background</h4>The myocyte enhancer factor 2 (MEF2) gene family is broadly expressed during the development and maintenance of muscle cells. Although a great deal has been elucidated concerning MEF2 transcription factors' regulation of specific gene expression in diverse programs and adaptive responses, little is known about the origin and evolution of the four members of the MEF2 gene family in vertebrates.<h4>Methodology/principal findings</h4>By phylogenetic analyses, we investigated the origin, conservation, and evolution of the four MEF2 genes. First, among the four MEF2 paralogous branches, MEF2B is clearly distant from the other three branches in vertebrates, mainly because it lacks the HJURP_C (Holliday junction recognition protein C-terminal) region. Second, three duplication events might have occurred to produce the four MEF2 paralogous genes and the latest duplication event occurred near the origin of vertebrates producing MEF2A and MEF2C. Third, the ratio (K(a)/K(s)) of non-synonymous to synonymous nucleotide substitution rates showed that MEF2B evolves faster than the other three MEF2 proteins despite purifying selection on all of the four MEF2 branches. Moreover, a pair model of M0 versus M3 showed that variable selection exists among MEF2 proteins, and branch-site analysis presented that sites 53 and 64 along the MEF2B branch are under positive selection. Finally, and interestingly, substitution rates showed that type II MADS genes (i.e., MEF2-like genes) evolve as slowly as type I MADS genes (i.e., SRF-like genes) in animals, which is inconsistent with the fact that type II MADS genes evolve much slower than type I MADS genes in plants.<h4>Conclusion</h4>Our findings shed light on the relationship of MEF2A, B, C, and D with functional conservation and evolution in vertebrates. This study provides a rationale for future experimental design to investigate distinct but overlapping regulatory roles of the four MEF2 genes in various tissues.
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spelling doaj.art-eab047a76af340daab573434a2f14be22022-12-21T23:10:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-03-0163e1733410.1371/journal.pone.0017334Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.Wenwu WuStefan de FolterXia ShenWenqian ZhangShiheng Tao<h4>Background</h4>The myocyte enhancer factor 2 (MEF2) gene family is broadly expressed during the development and maintenance of muscle cells. Although a great deal has been elucidated concerning MEF2 transcription factors' regulation of specific gene expression in diverse programs and adaptive responses, little is known about the origin and evolution of the four members of the MEF2 gene family in vertebrates.<h4>Methodology/principal findings</h4>By phylogenetic analyses, we investigated the origin, conservation, and evolution of the four MEF2 genes. First, among the four MEF2 paralogous branches, MEF2B is clearly distant from the other three branches in vertebrates, mainly because it lacks the HJURP_C (Holliday junction recognition protein C-terminal) region. Second, three duplication events might have occurred to produce the four MEF2 paralogous genes and the latest duplication event occurred near the origin of vertebrates producing MEF2A and MEF2C. Third, the ratio (K(a)/K(s)) of non-synonymous to synonymous nucleotide substitution rates showed that MEF2B evolves faster than the other three MEF2 proteins despite purifying selection on all of the four MEF2 branches. Moreover, a pair model of M0 versus M3 showed that variable selection exists among MEF2 proteins, and branch-site analysis presented that sites 53 and 64 along the MEF2B branch are under positive selection. Finally, and interestingly, substitution rates showed that type II MADS genes (i.e., MEF2-like genes) evolve as slowly as type I MADS genes (i.e., SRF-like genes) in animals, which is inconsistent with the fact that type II MADS genes evolve much slower than type I MADS genes in plants.<h4>Conclusion</h4>Our findings shed light on the relationship of MEF2A, B, C, and D with functional conservation and evolution in vertebrates. This study provides a rationale for future experimental design to investigate distinct but overlapping regulatory roles of the four MEF2 genes in various tissues.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21394201/pdf/?tool=EBI
spellingShingle Wenwu Wu
Stefan de Folter
Xia Shen
Wenqian Zhang
Shiheng Tao
Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
PLoS ONE
title Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
title_full Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
title_fullStr Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
title_full_unstemmed Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
title_short Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
title_sort vertebrate paralogous mef2 genes origin conservation and evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21394201/pdf/?tool=EBI
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AT xiashen vertebrateparalogousmef2genesoriginconservationandevolution
AT wenqianzhang vertebrateparalogousmef2genesoriginconservationandevolution
AT shihengtao vertebrateparalogousmef2genesoriginconservationandevolution