Cargando…

Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export

Skeletal muscle stem cells (also known as satellite cells [SCs]) are essential for muscle regeneration and the regenerative activities of SCs are intrinsically governed by gene regulatory mechanisms, but the post-transcriptional regulation in SCs remains largely unknown. N(6)-methyladenosine (m6A) m...

Descripción completa

Detalles Bibliográficos
Autores principales: Qiao, Yulong, Sun, Qiang, Chen, Xiaona, He, Liangqiang, Wang, Di, Su, Ruibao, Xue, Yuanchao, Sun, Hao, Wang, Huating
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089659/
https://www.ncbi.nlm.nih.gov/pubmed/36892464
http://dx.doi.org/10.7554/eLife.82703
_version_ 1785022808404787200
author Qiao, Yulong
Sun, Qiang
Chen, Xiaona
He, Liangqiang
Wang, Di
Su, Ruibao
Xue, Yuanchao
Sun, Hao
Wang, Huating
author_facet Qiao, Yulong
Sun, Qiang
Chen, Xiaona
He, Liangqiang
Wang, Di
Su, Ruibao
Xue, Yuanchao
Sun, Hao
Wang, Huating
author_sort Qiao, Yulong
collection PubMed
description Skeletal muscle stem cells (also known as satellite cells [SCs]) are essential for muscle regeneration and the regenerative activities of SCs are intrinsically governed by gene regulatory mechanisms, but the post-transcriptional regulation in SCs remains largely unknown. N(6)-methyladenosine (m6A) modification of RNAs is the most pervasive and highly conserved RNA modification in eukaryotic cells; it exerts powerful impact on almost all aspects of mRNA processing that is mainly endowed by its binding with m6A reader proteins. In this study, we investigate the previously uncharacterized regulatory roles of YTHDC1, an m6A reader in mouse SCs. Our results demonstrate that YTHDC1 is an essential regulator of SC activation and proliferation upon acute injury-induced muscle regeneration. The induction of YTHDC1 is indispensable for SC activation and proliferation; thus, inducible YTHDC1 depletion almost abolishes SC regenerative capacity. Mechanistically, transcriptome-wide profiling using LACE-seq in both SCs and mouse C2C12 myoblasts identifies m6A-mediated binding targets of YTHDC1. Next, splicing analysis defines splicing mRNA targets of m6A-YTHDC1. Furthermore, nuclear export analysis also leads to the identification of potential mRNA export targets of m6A-YTHDC1 in SCs and C2C12 myoblasts;interestingly, some mRNAs can be regulated at both splicing and export levels. Lastly, we map YTHDC1 interacting protein partners in myoblasts and unveil a myriad of factors governing mRNA splicing, nuclear export, and transcription, among which hnRNPG appears to be a bona fide interacting partner of YTHDC1. Altogether, our findings uncover YTHDC1 as an essential factor controlling SC regenerative ability through multifaceted gene regulatory mechanisms in mouse myoblast cells.
format Online
Article
Text
id pubmed-10089659
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-100896592023-04-12 Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export Qiao, Yulong Sun, Qiang Chen, Xiaona He, Liangqiang Wang, Di Su, Ruibao Xue, Yuanchao Sun, Hao Wang, Huating eLife Cell Biology Skeletal muscle stem cells (also known as satellite cells [SCs]) are essential for muscle regeneration and the regenerative activities of SCs are intrinsically governed by gene regulatory mechanisms, but the post-transcriptional regulation in SCs remains largely unknown. N(6)-methyladenosine (m6A) modification of RNAs is the most pervasive and highly conserved RNA modification in eukaryotic cells; it exerts powerful impact on almost all aspects of mRNA processing that is mainly endowed by its binding with m6A reader proteins. In this study, we investigate the previously uncharacterized regulatory roles of YTHDC1, an m6A reader in mouse SCs. Our results demonstrate that YTHDC1 is an essential regulator of SC activation and proliferation upon acute injury-induced muscle regeneration. The induction of YTHDC1 is indispensable for SC activation and proliferation; thus, inducible YTHDC1 depletion almost abolishes SC regenerative capacity. Mechanistically, transcriptome-wide profiling using LACE-seq in both SCs and mouse C2C12 myoblasts identifies m6A-mediated binding targets of YTHDC1. Next, splicing analysis defines splicing mRNA targets of m6A-YTHDC1. Furthermore, nuclear export analysis also leads to the identification of potential mRNA export targets of m6A-YTHDC1 in SCs and C2C12 myoblasts;interestingly, some mRNAs can be regulated at both splicing and export levels. Lastly, we map YTHDC1 interacting protein partners in myoblasts and unveil a myriad of factors governing mRNA splicing, nuclear export, and transcription, among which hnRNPG appears to be a bona fide interacting partner of YTHDC1. Altogether, our findings uncover YTHDC1 as an essential factor controlling SC regenerative ability through multifaceted gene regulatory mechanisms in mouse myoblast cells. eLife Sciences Publications, Ltd 2023-03-09 /pmc/articles/PMC10089659/ /pubmed/36892464 http://dx.doi.org/10.7554/eLife.82703 Text en © 2023, Qiao, Sun et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Qiao, Yulong
Sun, Qiang
Chen, Xiaona
He, Liangqiang
Wang, Di
Su, Ruibao
Xue, Yuanchao
Sun, Hao
Wang, Huating
Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title_full Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title_fullStr Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title_full_unstemmed Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title_short Nuclear m6A reader YTHDC1 promotes muscle stem cell activation/proliferation by regulating mRNA splicing and nuclear export
title_sort nuclear m6a reader ythdc1 promotes muscle stem cell activation/proliferation by regulating mrna splicing and nuclear export
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089659/
https://www.ncbi.nlm.nih.gov/pubmed/36892464
http://dx.doi.org/10.7554/eLife.82703
work_keys_str_mv AT qiaoyulong nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT sunqiang nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT chenxiaona nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT heliangqiang nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT wangdi nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT suruibao nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT xueyuanchao nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT sunhao nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport
AT wanghuating nuclearm6areaderythdc1promotesmusclestemcellactivationproliferationbyregulatingmrnasplicingandnuclearexport