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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
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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 |
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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 |
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