{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Li Z"],"funding":["the China Manned Space Flight Technology Project Chinese Space Station","National Natural Science Foundation of China","Key Research Program of Chinese Academy of Sciences","National Key Research and Development Program of China","Youth Innovation Promotion Association of the Chinese Academy of Sciences"],"pagination":["8"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12831727"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(1)"],"pubmed_abstract":["Skeletal muscle aging is characterized by a functional decline in muscle stem cells (MuSCs), yet the key regulatory mechanisms driving this deterioration remain poorly understood. By integrating transcriptomic profiles from aged MuSCs with data from C2C12 cells exposed to spaceflight conditions (which mimic an aging-like phenotype), we identified MORF4-related gene on chromosome 15 (MRG15) as a putative epigenetic regulator involved in age-related myogenic decline. Using a MuSC-specific inducible knockout (iKO) mouse model, we found that loss of MRG15 severely compromises myogenic differentiation and muscle regeneration. Subsequent RNA sequencing of iKO MuSCs, combined with ChIP-seq analysis of histone modifications, revealed that MRG15 modulates the chromatin landscape of myogenic genes t"],"journal":["Cell regeneration (London, England)"],"pubmed_title":["MRG15 decline in aged/injured MuSCs hinders regeneration via differentiation defects."],"pmcid":["PMC12831727"],"funding_grant_id":["32200686","ZDBS-ZRKJZ-TLC004","2021261","91957205","YYWT-0901-EXP-05","32371246","2021YFA1100500"],"pubmed_authors":["Ma R","Li Y","Li Z","Ma M","Shen S","Ding Q","Ying H","Wu Y","Kong W"],"additional_accession":[]},"is_claimable":false,"name":"MRG15 decline in aged/injured MuSCs hinders regeneration via differentiation defects.","description":"Skeletal muscle aging is characterized by a functional decline in muscle stem cells (MuSCs), yet the key regulatory mechanisms driving this deterioration remain poorly understood. By integrating transcriptomic profiles from aged MuSCs with data from C2C12 cells exposed to spaceflight conditions (which mimic an aging-like phenotype), we identified MORF4-related gene on chromosome 15 (MRG15) as a putative epigenetic regulator involved in age-related myogenic decline. Using a MuSC-specific inducible knockout (iKO) mouse model, we found that loss of MRG15 severely compromises myogenic differentiation and muscle regeneration. Subsequent RNA sequencing of iKO MuSCs, combined with ChIP-seq analysis of histone modifications, revealed that MRG15 modulates the chromatin landscape of myogenic genes t","dates":{"release":"2026-01-01T00:00:00Z","publication":"2026 Jan","modification":"2026-07-15T06:07:35.773Z","creation":"2026-07-01T03:07:42.438Z"},"accession":"S-EPMC12831727","cross_references":{"pubmed":["41580578"],"doi":["10.1186/s13619-026-00279-9"]}}