The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus

To investigate prenatal muscle satellite cell (MuSC) development and the associated epigenetic modifications in yak. Here, we conducted morphological and protein co-localization analyses of fetal longissimus dorsi muscle at various developmental stages using histology and immunofluorescence staining...

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Main Authors: Guoxiong Nan, Wei Peng, Shangrong Xu, Guowen Wang, Jun Zhang
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Biology
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Online Access:https://www.mdpi.com/2079-7737/13/12/1091
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author Guoxiong Nan
Wei Peng
Shangrong Xu
Guowen Wang
Jun Zhang
author_facet Guoxiong Nan
Wei Peng
Shangrong Xu
Guowen Wang
Jun Zhang
author_sort Guoxiong Nan
collection DOAJ
description To investigate prenatal muscle satellite cell (MuSC) development and the associated epigenetic modifications in yak. Here, we conducted morphological and protein co-localization analyses of fetal longissimus dorsi muscle at various developmental stages using histology and immunofluorescence staining methods. Our study observed that primary muscle fibers began forming at 40 days of gestation, fully developed by 11 weeks, and secondary muscle fibers were predominantly formed by around 105 days. Throughout development, MuSCs were mainly located between the muscle fiber membrane and the basement membrane, acting as a reserve for the stem cell pool. MuSCs appeared within myotubes only during critical phases of primary and secondary muscle fiber formation. The proliferation of MuSCs gradually decreases until birth. MuSCs with 5mC modification show a trend of increasing first and then decreasing. MuSCs with 5hmC modification also present a dynamic change trend. The 41st day and 11th week are the critical periods for the changes of both. From the 11th week to around the 110th day of gestation, the modification effect of histone H3K4me3 is crucial for MuSCs during the development of the fetal longissimus dorsi muscle. Combined, our data identify key time points for yak fetal skeletal muscle growth and development and demonstrate that DNA methylation and histone modifications in MuSCs are closely related to this process, offering a valuable basis for future research into the molecular mechanisms underlying yak muscle development.
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spelling doaj-art-3a95c60c084f49ec91fd25fd7c79cd9f2024-12-27T14:12:15ZengMDPI AGBiology2079-77372024-12-011312109110.3390/biology13121091The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak FetusGuoxiong Nan0Wei Peng1Shangrong Xu2Guowen Wang3Jun Zhang4College of Animal Husbandry and Veterinary Science, Qinghai University, Xining 810016, ChinaCollege of Animal Husbandry and Veterinary Science, Qinghai University, Xining 810016, ChinaCollege of Animal Husbandry and Veterinary Science, Qinghai University, Xining 810016, ChinaCollege of Animal Husbandry and Veterinary Science, Qinghai University, Xining 810016, ChinaCollege of Animal Husbandry and Veterinary Science, Qinghai University, Xining 810016, ChinaTo investigate prenatal muscle satellite cell (MuSC) development and the associated epigenetic modifications in yak. Here, we conducted morphological and protein co-localization analyses of fetal longissimus dorsi muscle at various developmental stages using histology and immunofluorescence staining methods. Our study observed that primary muscle fibers began forming at 40 days of gestation, fully developed by 11 weeks, and secondary muscle fibers were predominantly formed by around 105 days. Throughout development, MuSCs were mainly located between the muscle fiber membrane and the basement membrane, acting as a reserve for the stem cell pool. MuSCs appeared within myotubes only during critical phases of primary and secondary muscle fiber formation. The proliferation of MuSCs gradually decreases until birth. MuSCs with 5mC modification show a trend of increasing first and then decreasing. MuSCs with 5hmC modification also present a dynamic change trend. The 41st day and 11th week are the critical periods for the changes of both. From the 11th week to around the 110th day of gestation, the modification effect of histone H3K4me3 is crucial for MuSCs during the development of the fetal longissimus dorsi muscle. Combined, our data identify key time points for yak fetal skeletal muscle growth and development and demonstrate that DNA methylation and histone modifications in MuSCs are closely related to this process, offering a valuable basis for future research into the molecular mechanisms underlying yak muscle development.https://www.mdpi.com/2079-7737/13/12/1091yakskeletal musclemuscle satellite cellepigenetic modification
spellingShingle Guoxiong Nan
Wei Peng
Shangrong Xu
Guowen Wang
Jun Zhang
The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
Biology
yak
skeletal muscle
muscle satellite cell
epigenetic modification
title The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
title_full The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
title_fullStr The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
title_full_unstemmed The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
title_short The Development of Prenatal Muscle Satellite Cells (MuSCs) and Their Epigenetic Modifications During Skeletal Muscle Development in Yak Fetus
title_sort development of prenatal muscle satellite cells muscs and their epigenetic modifications during skeletal muscle development in yak fetus
topic yak
skeletal muscle
muscle satellite cell
epigenetic modification
url https://www.mdpi.com/2079-7737/13/12/1091
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