Cargando…

A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken

BACKGROUND: Development of skeletal muscle is closely related to broiler production traits. The myocyte-specific enhancer binding factor (MEF) 2D gene (MEF2D) and its variant transcripts play important parts in myogenesis. METHODS: To identify the transcript variants of chicken MEF2D gene and their...

Descripción completa

Detalles Bibliográficos
Autores principales: Ouyang, Hongjia, Yu, Jiao, Chen, Xiaolan, Wang, Zhijun, Nie, Qinghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006513/
https://www.ncbi.nlm.nih.gov/pubmed/32117604
http://dx.doi.org/10.7717/peerj.8351
_version_ 1783495160132272128
author Ouyang, Hongjia
Yu, Jiao
Chen, Xiaolan
Wang, Zhijun
Nie, Qinghua
author_facet Ouyang, Hongjia
Yu, Jiao
Chen, Xiaolan
Wang, Zhijun
Nie, Qinghua
author_sort Ouyang, Hongjia
collection PubMed
description BACKGROUND: Development of skeletal muscle is closely related to broiler production traits. The myocyte-specific enhancer binding factor (MEF) 2D gene (MEF2D) and its variant transcripts play important parts in myogenesis. METHODS: To identify the transcript variants of chicken MEF2D gene and their function, this study cloned chicken MEF2D gene and identified its transcript variants from different tissue samples. The expression levels of different transcripts of MEF2D gene in different tissues and different periods were measured, and their effects on myoblast proliferation and differentiation were investigated. Variations in MEF2D were identified and association analysis with chicken production traits carried out. RESULTS: Four novel transcript variants of MEF2D were obtained, all of which contained highly conserved sequences, including MADS-Box and MEF2-Domain functional regions. Transcript MEF2D-V4 was expressed specifically in muscle, and its expression was increased during embryonic muscle development. The MEF2D-V4 could promote differentiation of chicken myoblasts and its expression was regulated by RBFOX2. The single nucleotide polymorphism g.36186C > T generated a TAG stop codon, caused MEF2D-V4 to terminate translation early, and was associated with several growth traits, especially on early body weight. CONCLUSION: We cloned the muscle-specific transcript of MEF2D and preliminarily revealed its role in embryonic muscle development.
format Online
Article
Text
id pubmed-7006513
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-70065132020-02-28 A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken Ouyang, Hongjia Yu, Jiao Chen, Xiaolan Wang, Zhijun Nie, Qinghua PeerJ Molecular Biology BACKGROUND: Development of skeletal muscle is closely related to broiler production traits. The myocyte-specific enhancer binding factor (MEF) 2D gene (MEF2D) and its variant transcripts play important parts in myogenesis. METHODS: To identify the transcript variants of chicken MEF2D gene and their function, this study cloned chicken MEF2D gene and identified its transcript variants from different tissue samples. The expression levels of different transcripts of MEF2D gene in different tissues and different periods were measured, and their effects on myoblast proliferation and differentiation were investigated. Variations in MEF2D were identified and association analysis with chicken production traits carried out. RESULTS: Four novel transcript variants of MEF2D were obtained, all of which contained highly conserved sequences, including MADS-Box and MEF2-Domain functional regions. Transcript MEF2D-V4 was expressed specifically in muscle, and its expression was increased during embryonic muscle development. The MEF2D-V4 could promote differentiation of chicken myoblasts and its expression was regulated by RBFOX2. The single nucleotide polymorphism g.36186C > T generated a TAG stop codon, caused MEF2D-V4 to terminate translation early, and was associated with several growth traits, especially on early body weight. CONCLUSION: We cloned the muscle-specific transcript of MEF2D and preliminarily revealed its role in embryonic muscle development. PeerJ Inc. 2020-02-04 /pmc/articles/PMC7006513/ /pubmed/32117604 http://dx.doi.org/10.7717/peerj.8351 Text en © 2020 Ouyang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Molecular Biology
Ouyang, Hongjia
Yu, Jiao
Chen, Xiaolan
Wang, Zhijun
Nie, Qinghua
A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title_full A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title_fullStr A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title_full_unstemmed A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title_short A novel transcript of MEF2D promotes myoblast differentiation and its variations associated with growth traits in chicken
title_sort novel transcript of mef2d promotes myoblast differentiation and its variations associated with growth traits in chicken
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006513/
https://www.ncbi.nlm.nih.gov/pubmed/32117604
http://dx.doi.org/10.7717/peerj.8351
work_keys_str_mv AT ouyanghongjia anoveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT yujiao anoveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT chenxiaolan anoveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT wangzhijun anoveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT nieqinghua anoveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT ouyanghongjia noveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT yujiao noveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT chenxiaolan noveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT wangzhijun noveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken
AT nieqinghua noveltranscriptofmef2dpromotesmyoblastdifferentiationanditsvariationsassociatedwithgrowthtraitsinchicken