author_facet Sun, Wenqiang
Hu, Shenqiang
Hu, Jiwei
Qiu, Jiamin
Yang, Shuang
Hu, Bo
Gan, Xiang
Liu, Hehe
Li, Liang
Wang, Jiwen
Sun, Wenqiang
Hu, Shenqiang
Hu, Jiwei
Qiu, Jiamin
Yang, Shuang
Hu, Bo
Gan, Xiang
Liu, Hehe
Li, Liang
Wang, Jiwen
author Sun, Wenqiang
Hu, Shenqiang
Hu, Jiwei
Qiu, Jiamin
Yang, Shuang
Hu, Bo
Gan, Xiang
Liu, Hehe
Li, Liang
Wang, Jiwen
spellingShingle Sun, Wenqiang
Hu, Shenqiang
Hu, Jiwei
Qiu, Jiamin
Yang, Shuang
Hu, Bo
Gan, Xiang
Liu, Hehe
Li, Liang
Wang, Jiwen
Bioscience Reports
Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
Cell Biology
Molecular Biology
Biochemistry
Biophysics
author_sort sun, wenqiang
spelling Sun, Wenqiang Hu, Shenqiang Hu, Jiwei Qiu, Jiamin Yang, Shuang Hu, Bo Gan, Xiang Liu, Hehe Li, Liang Wang, Jiwen 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20182152 <jats:title>Abstract</jats:title> <jats:p>Akirin1 is found to be involved in myoblast differentiation. However, the mechanism by which the Akirin1 gene regulates myoblast differentiation still remains unclear. In the present study, we found that ectopic expression of Akirin1 promoted myoblast differentiation by increasing the expression of myogenic regulatory factor (MRF) 4 (MRF4) and myocyte enhancer factor 2B (MEF2B) mRNA. Additionally, we showed that ectopic Akirin1 induced cell cycle arrest by up-regulating p21 mRNA. To further uncover the mechanism by which Akirin1 promotes myoblast differentiation, we showed that the enhanced Akirin1 increased the mRNA expression of P38α. Importantly, the enhanced MRF4 expression by Akirin1 can be abrogated by treatment of SB203580, a p38 inhibitor. Similarly, we found that enhanced MEF2B expression by Akirin1 can be abrogated by treatment with LY294002, a PI3K inhibitor. Together, our results indicate that Akirin1 promotes myoblast differentiation by acting on the p38 and PI3K pathways and subsequently inducing the expression of myoblast differentiation factors.</jats:p> Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors Bioscience Reports
doi_str_mv 10.1042/bsr20182152
facet_avail Online
Free
finc_class_facet Biologie
Chemie und Pharmazie
Physik
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE4MjE1Mg
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE4MjE1Mg
institution DE-Zwi2
DE-D161
DE-Zi4
DE-Gla1
DE-15
DE-Pl11
DE-Rs1
DE-14
DE-105
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
imprint Portland Press Ltd., 2019
imprint_str_mv Portland Press Ltd., 2019
issn 0144-8463
1573-4935
issn_str_mv 0144-8463
1573-4935
language English
mega_collection Portland Press Ltd. (CrossRef)
match_str sun2019akirin1promotesmyoblastdifferentiationbymodulatingmultiplemyoblastdifferentiationfactors
publishDateSort 2019
publisher Portland Press Ltd.
recordtype ai
record_format ai
series Bioscience Reports
source_id 49
title Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_unstemmed Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_full Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_fullStr Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_full_unstemmed Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_short Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_sort akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
topic Cell Biology
Molecular Biology
Biochemistry
Biophysics
url http://dx.doi.org/10.1042/bsr20182152
publishDate 2019
physical
description <jats:title>Abstract</jats:title> <jats:p>Akirin1 is found to be involved in myoblast differentiation. However, the mechanism by which the Akirin1 gene regulates myoblast differentiation still remains unclear. In the present study, we found that ectopic expression of Akirin1 promoted myoblast differentiation by increasing the expression of myogenic regulatory factor (MRF) 4 (MRF4) and myocyte enhancer factor 2B (MEF2B) mRNA. Additionally, we showed that ectopic Akirin1 induced cell cycle arrest by up-regulating p21 mRNA. To further uncover the mechanism by which Akirin1 promotes myoblast differentiation, we showed that the enhanced Akirin1 increased the mRNA expression of P38α. Importantly, the enhanced MRF4 expression by Akirin1 can be abrogated by treatment of SB203580, a p38 inhibitor. Similarly, we found that enhanced MEF2B expression by Akirin1 can be abrogated by treatment with LY294002, a PI3K inhibitor. Together, our results indicate that Akirin1 promotes myoblast differentiation by acting on the p38 and PI3K pathways and subsequently inducing the expression of myoblast differentiation factors.</jats:p>
container_issue 3
container_start_page 0
container_title Bioscience Reports
container_volume 39
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792329889843511299
geogr_code not assigned
last_indexed 2024-03-01T13:16:22.141Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Akirin1+promotes+myoblast+differentiation+by+modulating+multiple+myoblast+differentiation+factors&rft.date=2019-03-29&genre=article&issn=1573-4935&volume=39&issue=3&jtitle=Bioscience+Reports&atitle=Akirin1+promotes+myoblast+differentiation+by+modulating+multiple+myoblast+differentiation+factors&aulast=Wang&aufirst=Jiwen&rft_id=info%3Adoi%2F10.1042%2Fbsr20182152&rft.language%5B0%5D=eng
SOLR
_version_ 1792329889843511299
author Sun, Wenqiang, Hu, Shenqiang, Hu, Jiwei, Qiu, Jiamin, Yang, Shuang, Hu, Bo, Gan, Xiang, Liu, Hehe, Li, Liang, Wang, Jiwen
author_facet Sun, Wenqiang, Hu, Shenqiang, Hu, Jiwei, Qiu, Jiamin, Yang, Shuang, Hu, Bo, Gan, Xiang, Liu, Hehe, Li, Liang, Wang, Jiwen, Sun, Wenqiang, Hu, Shenqiang, Hu, Jiwei, Qiu, Jiamin, Yang, Shuang, Hu, Bo, Gan, Xiang, Liu, Hehe, Li, Liang, Wang, Jiwen
author_sort sun, wenqiang
container_issue 3
container_start_page 0
container_title Bioscience Reports
container_volume 39
description <jats:title>Abstract</jats:title> <jats:p>Akirin1 is found to be involved in myoblast differentiation. However, the mechanism by which the Akirin1 gene regulates myoblast differentiation still remains unclear. In the present study, we found that ectopic expression of Akirin1 promoted myoblast differentiation by increasing the expression of myogenic regulatory factor (MRF) 4 (MRF4) and myocyte enhancer factor 2B (MEF2B) mRNA. Additionally, we showed that ectopic Akirin1 induced cell cycle arrest by up-regulating p21 mRNA. To further uncover the mechanism by which Akirin1 promotes myoblast differentiation, we showed that the enhanced Akirin1 increased the mRNA expression of P38α. Importantly, the enhanced MRF4 expression by Akirin1 can be abrogated by treatment of SB203580, a p38 inhibitor. Similarly, we found that enhanced MEF2B expression by Akirin1 can be abrogated by treatment with LY294002, a PI3K inhibitor. Together, our results indicate that Akirin1 promotes myoblast differentiation by acting on the p38 and PI3K pathways and subsequently inducing the expression of myoblast differentiation factors.</jats:p>
doi_str_mv 10.1042/bsr20182152
facet_avail Online, Free
finc_class_facet Biologie, Chemie und Pharmazie, Physik
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Mi9ic3IyMDE4MjE1Mg
imprint Portland Press Ltd., 2019
imprint_str_mv Portland Press Ltd., 2019
institution DE-Zwi2, DE-D161, DE-Zi4, DE-Gla1, DE-15, DE-Pl11, DE-Rs1, DE-14, DE-105, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1
issn 0144-8463, 1573-4935
issn_str_mv 0144-8463, 1573-4935
language English
last_indexed 2024-03-01T13:16:22.141Z
match_str sun2019akirin1promotesmyoblastdifferentiationbymodulatingmultiplemyoblastdifferentiationfactors
mega_collection Portland Press Ltd. (CrossRef)
physical
publishDate 2019
publishDateSort 2019
publisher Portland Press Ltd.
record_format ai
recordtype ai
series Bioscience Reports
source_id 49
spelling Sun, Wenqiang Hu, Shenqiang Hu, Jiwei Qiu, Jiamin Yang, Shuang Hu, Bo Gan, Xiang Liu, Hehe Li, Liang Wang, Jiwen 0144-8463 1573-4935 Portland Press Ltd. Cell Biology Molecular Biology Biochemistry Biophysics http://dx.doi.org/10.1042/bsr20182152 <jats:title>Abstract</jats:title> <jats:p>Akirin1 is found to be involved in myoblast differentiation. However, the mechanism by which the Akirin1 gene regulates myoblast differentiation still remains unclear. In the present study, we found that ectopic expression of Akirin1 promoted myoblast differentiation by increasing the expression of myogenic regulatory factor (MRF) 4 (MRF4) and myocyte enhancer factor 2B (MEF2B) mRNA. Additionally, we showed that ectopic Akirin1 induced cell cycle arrest by up-regulating p21 mRNA. To further uncover the mechanism by which Akirin1 promotes myoblast differentiation, we showed that the enhanced Akirin1 increased the mRNA expression of P38α. Importantly, the enhanced MRF4 expression by Akirin1 can be abrogated by treatment of SB203580, a p38 inhibitor. Similarly, we found that enhanced MEF2B expression by Akirin1 can be abrogated by treatment with LY294002, a PI3K inhibitor. Together, our results indicate that Akirin1 promotes myoblast differentiation by acting on the p38 and PI3K pathways and subsequently inducing the expression of myoblast differentiation factors.</jats:p> Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors Bioscience Reports
spellingShingle Sun, Wenqiang, Hu, Shenqiang, Hu, Jiwei, Qiu, Jiamin, Yang, Shuang, Hu, Bo, Gan, Xiang, Liu, Hehe, Li, Liang, Wang, Jiwen, Bioscience Reports, Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors, Cell Biology, Molecular Biology, Biochemistry, Biophysics
title Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_full Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_fullStr Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_full_unstemmed Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_short Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_sort akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
title_unstemmed Akirin1 promotes myoblast differentiation by modulating multiple myoblast differentiation factors
topic Cell Biology, Molecular Biology, Biochemistry, Biophysics
url http://dx.doi.org/10.1042/bsr20182152