References
- Bilodeau, S., Kagey, M.H., Frampton, G.M., Rahl, P.B., and Young, R.A. (2009). SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell state. Genes Dev. 23, 2484-2489. https://doi.org/10.1101/gad.1837309
- Blais, A., Tsikitis, M., Acosta-Alvear, D., Sharan, R., Kluger, Y., and Dynlacht, B.D. (2005). An initial blueprint for myogenic differentiation. Genes Dev. 19, 553-569. https://doi.org/10.1101/gad.1281105
- Blum, R., and Dynlacht, B.D. (2013). The role of MyoD1 and histone modifications in the activation of muscle enhancers. Epigenetics 8, 778-784. https://doi.org/10.4161/epi.25441
- Cao, Y., Kumar, R.M., Penn, B.H., Berkes, C.A., Kooperberg, C., Boyer, L.A., Young, R.A., and Tapscott, S.J. (2006). Global and gene-specific analyses show distinct roles for Myod and Myog at a common set of promoters. EMBO J. 25, 502-511. https://doi.org/10.1038/sj.emboj.7600958
- Caretti, G., Di Padova, M., Micales, B., Lyons, G.E., and Sartorelli, V. (2004). The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation. Genes Dev. 18, 2627-2638. https://doi.org/10.1101/gad.1241904
- Chen, C.M., Kraut, N., Groudine, M., and Weintraub, H. (1996). I-mf, a novel myogenic repressor, interacts with members of the MyoD family. Cell 86, 731-741. https://doi.org/10.1016/S0092-8674(00)80148-8
- Choi, J., Jang, H., Kim, H., Lee, J.H., Kim, S.T., Cho, E.J., and Youn, H.D. (2014). Modulation of lysine methylation in myocyte enhancer factor 2 during skeletal muscle cell differentiation. Nucleic Acids Res. 42, 224-234. https://doi.org/10.1093/nar/gkt873
- Delgado, I., Huang, X., Jones, S., Zhang, L., Hatcher, R., Gao, B., and Zhang, P. (2003). Dynamic gene expression during the onset of myoblast differentiation in vitro. Genomics 82, 109-121. https://doi.org/10.1016/S0888-7543(03)00104-6
- Dilworth, F.J., Seaver, K.J., Fishburn, A.L., Htet, S.L., and Tapscott, S.J. (2004). In vitro transcription system delineates the distinct roles of the coactivators pCAF and p300 during MyoD/E47-dependent transactivation. Proc. Natl. Acad. Sci. USA 101, 11593-11598. https://doi.org/10.1073/pnas.0404192101
- Dodge, J.E., Kang, Y.K., Beppu, H., Lei, H., and Li, E. (2004). Histone H3-K9 methyltransferase ESET is essential for early development. Mol. Cell. Biol. 24, 2478-2486. https://doi.org/10.1128/MCB.24.6.2478-2486.2004
- Eom, G.H., Kim, K.B., Kim, J.H., Kim, J.Y., Kim, J.R., Kee, H.J., Kim, D.W., Choe, N., Park, H.J., Son, H.J., et al. (2011). Histone methyltransferase SETD3 regulates muscle differentiation. J. Biol. Chem. 286, 34733-34742. https://doi.org/10.1074/jbc.M110.203307
- Hasty, P., Bradley, A., Morris, J.H., Edmondson, D.G., Venuti, J.M., Olson, E.N., and Klein, W.H. (1993). Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene. Nature 364, 501-506. https://doi.org/10.1038/364501a0
- Jen, Y., Weintraub, H., and Benezra, R. (1992). Overexpression of Id protein inhibits the muscle differentiation program: in vivo association of Id with E2A proteins. Genes Dev 6, 1466-1479. https://doi.org/10.1101/gad.6.8.1466
- Lassar, A.B., Davis, R.L., Wright, W.E., Kadesch, T., Murre, C., Voronova, A., Baltimore, D., and Weintraub, H. (1991). Functional activity of myogenic HLH proteins requires hetero-oligomerization with E12/E47-like proteins in vivo. Cell 66, 305-315. https://doi.org/10.1016/0092-8674(91)90620-E
- Lee, H., Habas, R., and Abate-Shen, C. (2004). MSX1 cooperates with histone H1b for inhibition of transcription and myogenesis. Science 304, 1675-1678. https://doi.org/10.1126/science.1098096
- Ling, B.M., Bharathy, N., Chung, T.K., Kok, W.K., Li, S., Tan, Y.H., Rao, V.K., Gopinadhan, S., Sartorelli, V., Walsh, M.J., et al. (2012). Lysine methyltransferase G9a methylates the transcription factor MyoD and regulates skeletal muscle differentiation. Proc. Natl. Acad. Sci. USA 109, 841-846. https://doi.org/10.1073/pnas.1111628109
- Mal, A.K. (2006). Histone methyltransferase Suv39h1 represses MyoD-stimulated myogenic differentiation. EMBO J. 25, 3323-3334. https://doi.org/10.1038/sj.emboj.7601229
- Mal, A., and Harter, M.L. (2003). MyoD is functionally linked to the silencing of a muscle-specific regulatory gene prior to skeletal myogenesis. Proc. Natl. Acad. Sci. USA 100, 1735-1739. https://doi.org/10.1073/pnas.0437843100
- Mal, A., Sturniolo, M., Schiltz, R.L., Ghosh, M.K., and Harter, M.L. (2001). A role for histone deacetylase HDAC1 in modulating the transcriptional activity of MyoD: inhibition of the myogenic program. EMBO J. 20, 1739-1753. https://doi.org/10.1093/emboj/20.7.1739
- Mitchell, P.O., Mills, T., O'Connor, R.S., Kline, E.R., Graubert, T., Dzierzak, E., and Pavlath, G.K. (2005). Sca-1 negatively regulates proliferation and differentiation of muscle cells. Dev. Biol. 283, 240-252. https://doi.org/10.1016/j.ydbio.2005.04.016
- Molkentin, J.D., Black, B.L., Martin, J.F., and Olson, E.N. (1995). Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins. Cell 83, 1125-1136. https://doi.org/10.1016/0092-8674(95)90139-6
- Moran, J.L., Li, Y., Hill, A.A., Mounts, W.M., and Miller, C.P. (2002). Gene expression changes during mouse skeletal myoblast differentiation revealed by transcriptional profiling. Physiol. Genomics 10, 103-111. https://doi.org/10.1152/physiolgenomics.00011.2002
- Puri, P.L., Avantaggiati, M.L., Balsano, C., Sang, N., Graessmann, A., Giordano, A., and Levrero, M. (1997a). p300 is required for MyoD-dependent cell cycle arrest and muscle-specific gene transcription. EMBO J. 16, 369-383. https://doi.org/10.1093/emboj/16.2.369
- Puri, P.L., Sartorelli, V., Yang. X.J., Hamamori. Y., Ogryzko. V.V., Howard. B.H., Kedes. L., Wang. J.Y., Graessmann. A., Nakatani. Y., and Levrero, M. (1997b). Differential roles of p300 and PCAF acetyltransferases in muscle differentiation. Mol. Cell 1 35-45. https://doi.org/10.1016/S1097-2765(00)80005-2
- Rao, S.S., and Kohtz, D.S. (1995). Positive and negative regulation of D-type cyclin expression in skeletal myoblasts by basic fibroblast growth factor and transforming growth factor beta. A role for cyclin D1 in control of myoblast differentiation. J. Biol. Chem. 270, 4093-4100. https://doi.org/10.1074/jbc.270.8.4093
- Rudnicki, M.A., Schnegelsberg, P.N., Stead, R.H., Braun, T., Arnold, H.H., and Jaenisch, R. (1993). MyoD or Myf-5 is required for the formation of skeletal muscle. Cell 75, 1351-1359. https://doi.org/10.1016/0092-8674(93)90621-V
- Sabourin, L.A., and Rudnicki, M.A. (2000). The molecular regulation of myogenesis. Clin. Genet. 57, 16-25.
- Sartorelli, V., and Caretti, G. (2005). Mechanisms underlying the transcriptional regulation of skeletal myogenesis. Curr. Opin. Genet. Dev. 15, 528-535. https://doi.org/10.1016/j.gde.2005.04.015
- Sartorelli, V., and Juan, A.H. (2011). Sculpting chromatin beyond the double helix: epigenetic control of skeletal myogenesis. Curr. Top. Dev. Biol. 96, 57-83. https://doi.org/10.1016/B978-0-12-385940-2.00003-6
- Schultz, D.C., Ayyanathan, K., Negorev, D., Maul, G.G., and Rauscher, F.J., 3rd (2002). SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteins. Genes Dev. 16, 919-932. https://doi.org/10.1101/gad.973302
- Seenundun, S., Rampalli, S., Liu, Q.C., Aziz, A., Palii, C., Hong, S., Blais, A., Brand, M., Ge, K., and Dilworth, F.J. (2010). UTX mediates demethylation of H3K27me3 at muscle-specific genes during myogenesis. EMBO J. 29, 1401-1411. https://doi.org/10.1038/emboj.2010.37
- Singh, J., Verma, N.K., Kansagra, S.M., Kate, B.N., and Dey, C.S. (2007). Altered PPARgamma expression inhibits myogenic differentiation in C2C12 skeletal muscle cells. Mol. Cell. Biochem. 294, 163-171. https://doi.org/10.1007/s11010-006-9256-x
- Song, Y.J., and Lee, H. (2011). YB1/p32, a nuclear Y-box binding protein 1, is a novel regulator of myoblast differentiation that interacts with Msx1 homeoprotein. Exp. Cell Res. 316, 517-529.
- Spicer, D.B., Rhee, J., Cheung, W.L., and Lassar, A.B. (1996). Inhibition of myogenic bHLH and MEF2 transcription factors by the bHLH protein Twist. Science 272, 1476-1480. https://doi.org/10.1126/science.272.5267.1476
- Takada, I., Mihara, M., Suzawa, M., Ohtake, F., Kobayashi, S., Igarashi, M., Youn, M.Y., Takeyama, K., Nakamura, T., Mezaki, Y., et al. (2007). A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation. Nat. Cell Biol. 9, 1273-1285. https://doi.org/10.1038/ncb1647
- Takada, I., Kouzmenko, A.P., and Kato, S. (2009). Wnt and PPARgamma signaling in osteoblastogenesis and adipogenesis. Nat. Rev. Rheumatol. 5, 442-447. https://doi.org/10.1038/nrrheum.2009.137
- Tan, S.L., Nishi, M., Ohtsuka, T., Matsui, T., Takemoto, K., Kamio-Miura, A., Aburatani, H., Shinkai, Y., and Kageyama, R. (2012). Essential roles of the histone methyltransferase ESET in the epigenetic control of neural progenitor cells during development. Development 139, 3806-3816. https://doi.org/10.1242/dev.082198
- Tao, Y., Neppl, R.L., Huang, Z.P., Chen, J., Tang, R.H., Cao, R., Zhang, Y., Jin, S.W., and Wang, D.Z. (2011). The histone methyltransferase Set7/9 promotes myoblast differentiation and myofibril assembly. J. Cell Biol. 194, 551-565. https://doi.org/10.1083/jcb.201010090
- Tapscott, S.J. (2005). The circuitry of a master switch: Myod and the regulation of skeletal muscle gene transcription. Development 132, 2685-2695. https://doi.org/10.1242/dev.01874
- Tapscott, S.J. (2005). The circuitry of a master switch: Myod and the regulation of skeletal muscle gene transcription. Development 132, 2685-2695. https://doi.org/10.1242/dev.01874
- Thayer, M.J., Tapscott, S.J., Davis, R.L., Wright, W.E., Lassar, A.B., and Weintraub, H. (1989). Positive autoregulation of the myogenic determination gene MyoD1. Cell 58, 241-248. https://doi.org/10.1016/0092-8674(89)90838-6
- Tomczak, K.K., Marinescu, V.D., Ramoni, M.F., Sanoudou, D., Montanaro, F., Han, M., Kunkel, L.M., Kohane, I.S., and Beggs, A.H. (2004). Expression profiling and identification of novel genes involved in myogenic differentiation. FASEB J. 18, 403-405. https://doi.org/10.1096/fj.03-0568fje
- Wang, J., Helin, K., Jin, P., and Nadal-Ginard, B. (1995). Inhibition of in vitro myogenic differentiation by cellular transcription factor E2F1. Cell Growth Differ. 6, 1299-1306.
- Yang, L., Lawson, K.A., Teteak, C.J., Zou, J., Hacquebord, J., Patterson, D., Ghatan, A.C., Mei, Q., Zielinska-Kwiatkowska, A., Bain, S.D., et al. (2013). ESET histone methyltransferase is essential to hypertrophic differentiation of growth plate chondrocytes and formation of epiphyseal plates. Dev. Biol. 380, 99-110. https://doi.org/10.1016/j.ydbio.2013.04.031
- Yuan, P., Han, J., Guo, G., Orlov, Y.L., Huss, M., Loh, Y.H., Yaw, L.P., Robson, P., Lim, B., and Ng, H.H. (2009). Eset partners with Oct4 to restrict extraembryonic trophoblast lineage potential in embryonic stem cells. Genes Dev. 23, 2507-2520. https://doi.org/10.1101/gad.1831909
- Zhang, W., Behringer, R.R., and Olson, E.N. (1995). Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib anomalies. Genes Dev. 9, 1388-1399. https://doi.org/10.1101/gad.9.11.1388
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