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Arginine methyltransferase CARM1/PRMT4 regulates endochondral ossification

BACKGROUND: Chondrogenesis and subsequent endochondral ossification are processes tightly regulated by the transcription factor Sox9 (SRY-related high mobility group-Box gene 9), but molecular mechanisms underlying this activity remain unclear. Here we report that coactivator-associated arginine met...

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Detalles Bibliográficos
Autores principales: Ito, Tatsuo, Yadav, Neelu, Lee, Jaeho, Furumatsu, Takayuki, Yamashita, Satoshi, Yoshida, Kenji, Taniguchi, Noboru, Hashimoto, Megumi, Tsuchiya, Megumi, Ozaki, Toshifumi, Lotz, Martin, Bedford, Mark T, Asahara, Hiroshi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2754437/
https://www.ncbi.nlm.nih.gov/pubmed/19725955
http://dx.doi.org/10.1186/1471-213X-9-47
Descripción
Sumario:BACKGROUND: Chondrogenesis and subsequent endochondral ossification are processes tightly regulated by the transcription factor Sox9 (SRY-related high mobility group-Box gene 9), but molecular mechanisms underlying this activity remain unclear. Here we report that coactivator-associated arginine methyltransferase 1 (CARM1) regulates chondrocyte proliferation via arginine methylation of Sox9. RESULTS: CARM1-null mice display delayed endochondral ossification and decreased chondrocyte proliferation. Conversely, cartilage development of CARM1 transgenic mice was accelerated. CARM1 specifically methylates Sox9 at its HMG domain in vivo and in vitro. Arg-methylation of Sox9 by CARM1 disrupts interaction of Sox9 with beta-catenin, regulating Cyclin D1 expression and cell cycle progression of chondrocytes. CONCLUSION: These results establish a role for CARM1 as an important regulator of chondrocyte proliferation during embryogenesis.