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Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development

The birth weight of chickens does not significantly affect the weight at slaughter, while the different growth rate after birth was one of the important reasons for the difference in slaughter weight. Also, the increase in chickens’ postnatal skeletal muscle weight is the main cause of the slaughter...

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Autores principales: Lin, Shudai, Xian, Mingjian, Ren, Tuanhui, Mo, Guodong, Zhang, Li, Zhang, Xiquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669902/
https://www.ncbi.nlm.nih.gov/pubmed/36407004
http://dx.doi.org/10.3389/fphys.2022.1033075
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author Lin, Shudai
Xian, Mingjian
Ren, Tuanhui
Mo, Guodong
Zhang, Li
Zhang, Xiquan
author_facet Lin, Shudai
Xian, Mingjian
Ren, Tuanhui
Mo, Guodong
Zhang, Li
Zhang, Xiquan
author_sort Lin, Shudai
collection PubMed
description The birth weight of chickens does not significantly affect the weight at slaughter, while the different growth rate after birth was one of the important reasons for the difference in slaughter weight. Also, the increase in chickens’ postnatal skeletal muscle weight is the main cause of the slaughter weight gain, but which genes are involved in this biological process is still unclear. In this study, by integrating four transcriptome datasets containing chicken muscles at different developmental times or different chicken tissues in public databases, a total of nine candidate genes that may be related to postnatal muscle development in chickens were obtained, including RPL3L, FBP2, ASB4, ASB15, CKMT2, PGAM1, YIPF7, PFKM, and LDHA. One of these candidate genes is RPL3L, whose 42 bp insertion/deletion (indel) mutation significantly correlated with multiple carcass traits in the F2 resource population from Xinghua chickens crossing with White Recessive Rock (WRR) chickens, including live weight, carcass weight, half eviscerated weight, eviscerated weight, breast meat weight, wing weight, leg muscle shear force, and breast muscle shear force. Also, there was a very significant difference between different genotypes of the RPL3L 42 bp indel mutation in these trains. Further experiments showed that RPL3L was highly expressed in chicken skeletal muscle, and its overexpression could promote the proliferation and inhibit the differentiation of chicken myoblasts by regulating ASB4 and ASB15 expression. Our findings demonstrated that the RPL3L 42 bp indel may be one of the molecular markers of chicken weight-related traits.
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spelling pubmed-96699022022-11-18 Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development Lin, Shudai Xian, Mingjian Ren, Tuanhui Mo, Guodong Zhang, Li Zhang, Xiquan Front Physiol Physiology The birth weight of chickens does not significantly affect the weight at slaughter, while the different growth rate after birth was one of the important reasons for the difference in slaughter weight. Also, the increase in chickens’ postnatal skeletal muscle weight is the main cause of the slaughter weight gain, but which genes are involved in this biological process is still unclear. In this study, by integrating four transcriptome datasets containing chicken muscles at different developmental times or different chicken tissues in public databases, a total of nine candidate genes that may be related to postnatal muscle development in chickens were obtained, including RPL3L, FBP2, ASB4, ASB15, CKMT2, PGAM1, YIPF7, PFKM, and LDHA. One of these candidate genes is RPL3L, whose 42 bp insertion/deletion (indel) mutation significantly correlated with multiple carcass traits in the F2 resource population from Xinghua chickens crossing with White Recessive Rock (WRR) chickens, including live weight, carcass weight, half eviscerated weight, eviscerated weight, breast meat weight, wing weight, leg muscle shear force, and breast muscle shear force. Also, there was a very significant difference between different genotypes of the RPL3L 42 bp indel mutation in these trains. Further experiments showed that RPL3L was highly expressed in chicken skeletal muscle, and its overexpression could promote the proliferation and inhibit the differentiation of chicken myoblasts by regulating ASB4 and ASB15 expression. Our findings demonstrated that the RPL3L 42 bp indel may be one of the molecular markers of chicken weight-related traits. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9669902/ /pubmed/36407004 http://dx.doi.org/10.3389/fphys.2022.1033075 Text en Copyright © 2022 Lin, Xian, Ren, Mo, Zhang and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Lin, Shudai
Xian, Mingjian
Ren, Tuanhui
Mo, Guodong
Zhang, Li
Zhang, Xiquan
Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title_full Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title_fullStr Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title_full_unstemmed Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title_short Mining of chicken muscle growth genes and the function of important candidate gene RPL3L in muscle development
title_sort mining of chicken muscle growth genes and the function of important candidate gene rpl3l in muscle development
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669902/
https://www.ncbi.nlm.nih.gov/pubmed/36407004
http://dx.doi.org/10.3389/fphys.2022.1033075
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