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...
Autores principales: | , , , , , , , , |
---|---|
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 |