Ret finger protein inhibits muscle differentiation by modulating serum response factor and enhancer of polycomb1open access
- Authors
- Kee, H. J.; Kim, J-R; Joung, H.; Choe, N.; Lee, S. E.; Eom, G. H.; Kim, J. C.; Geyer, S. H.; Jijiwa, M.; Kato, T.; Kawai, K.; Weninger, W. J.; Seo, S. B.; Nam, K-I; Jeong, M. H.; Takahashi, M.; Kook, H.
- Issue Date
- Jan-2012
- Publisher
- NATURE PUBLISHING GROUP
- Keywords
- enhancer of polycomb1; muscle differentiation; ret finger protein; serum response factor
- Citation
- CELL DEATH AND DIFFERENTIATION, v.19, no.1, pp 121 - 131
- Pages
- 11
- Journal Title
- CELL DEATH AND DIFFERENTIATION
- Volume
- 19
- Number
- 1
- Start Page
- 121
- End Page
- 131
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20603
- DOI
- 10.1038/cdd.2011.72
- ISSN
- 1350-9047
1476-5403
- Abstract
- Skeletal myogenesis is precisely regulated by multiple transcription factors. Previously, we demonstrated that enhancer of polycomb 1 (Epc1) induces skeletal muscle differentiation by potentiating serum response factor (SRF)-dependent muscle gene activation. Here, we report that an interacting partner of Epc1, ret finger protein (RFP), blocks skeletal muscle differentiation. Our findings show that RFP was highly expressed in skeletal muscles and was downregulated during myoblast differentiation. Forced expression of RFP delayed myoblast differentiation, whereas knockdown enhanced it. Epc1-induced enhancements of SRF-dependent multinucleation, transactivation of the skeletal a-actin promoter, binding of SRF to the serum response element, and muscle-specific gene induction were blocked by RFP. RFP interfered with the physical interaction between Epc1 and SRF. Muscles from rfp knockout mice (Rfp(-/-)) mice were bigger than those from wild-type mice, and the expression of SRF-dependent muscle-specific genes was upregulated. Myotube formation and myoblast differentiation were enhanced in Rfp(-/-) mice. Taken together, our findings highlight RFP as a novel regulator of muscle differentiation that acts by modulating the expression of SRF-dependent skeletal muscle-specific genes. Cell Death and Differentiation (2012) 19, 121-131; doi:10.1038/cdd.2011.72; published online 3 June 2011
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