Epigenetic regulation of skeletal myogenesis

References

• Buckingham M. Myogenic progenitor cells and skeletal myogenesis in vertebrates. Curr Opin Genet Dev 2006; 16:525 - 532
   PubMed Web of Science ®Google Scholar
• Snider L, Tapscott SJ. Emerging parallels in the generation and regeneration of skeletal muscle. Cell 2003; 113:811 - 812
   PubMed Web of Science ®Google Scholar
• Parker MH, Seale P, Rudnicki MA. Looking back to the embryo: defining transcriptional networks in adult myogenesis. Nat Rev Genet 2003; 4:497 - 507
   PubMed Web of Science ®Google Scholar
• Tajbakhsh S. Skeletal muscle stem cells in developmental versus regenerative myogenesis. J Intern Med 2009; 266:372 - 389
   PubMed Web of Science ®Google Scholar
• Buckingham M, Relaix F. The role of Pax genes in the development of tissues and organs: Pax3 and Pax7 regulate muscle progenitor cell functions. Annu Rev Cell Dev Biol 2007; 23:645 - 673
   PubMed Web of Science ®Google Scholar
• Cossu G, Tajbakhsh S, Buckingham M. How is myogenesis initiated in the embryo?. Trends Genet 1996; 12:218 - 223
   PubMed Web of Science ®Google Scholar
• Cossu G, Borello U. Wnt signaling and the activation of myogenesis in mammals. EMBO J 1999; 18:6867 - 6872
   PubMed Web of Science ®Google Scholar
• Hutcheson DA, Zhao J, Merrell A, Haldar M, Kardon G. Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for beta-catenin. Genes Dev 2009; 23:997 - 1013
   PubMed Web of Science ®Google Scholar
• Morgan JE, Partridge TA. Muscle satellite cells. Int J Biochem Cell Biol 2003; 35:1151 - 1156
   PubMed Web of Science ®Google Scholar
• Gros J, Manceau M, Thome V, Marcelle C. A common somitic origin for embryonic muscle progenitors and satellite cells. Nature 2005; 435:954 - 958
   PubMed Web of Science ®Google Scholar
• Relaix F, Rocancourt D, Mansouri A, Buckingham M. A Pax3/Pax7-dependent population of skeletal muscle progenitor cells. Nature 2005; 435:948 - 953
   PubMed Web of Science ®Google Scholar
• Kuang S, Rudnicki MA. The emerging biology of satellite cells and their therapeutic potential. Trends Mol Med 2008; 14:82 - 91
   PubMed Web of Science ®Google Scholar
• Cossu G, Kelly R, Tajbakhsh S, Di Donna S, Vivarelli E, Buckingham M. Activation of different myogenic pathways: myf-5 is induced by the neural tube and MyoD by the dorsal ectoderm in mouse paraxial mesoderm. Development 1996; 122:429 - 437
   PubMed Web of Science ®Google Scholar
• Pownall ME, Gustafsson MK, Emerson CP Jr. Myogenic regulatory factors and the specification of muscle progenitors in vertebrate embryos. Annu Rev Cell Dev Biol 2002; 18:747 - 783
   PubMed Web of Science ®Google Scholar
• Kassar-Duchossoy L, Gayraud-Morel B, Gomes D, Rocancourt D, Buckingham M, Shinin V, et al. Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice. Nature 2004; 431:466 - 471
   PubMed Web of Science ®Google Scholar
• Puri PL, Sartorelli V. Regulation of muscle regulatory factors by DNA-binding, interacting proteins, and post-transcriptional modifications. J Cell Physiol 2000; 185:155 - 173
   PubMed Web of Science ®Google Scholar
• Molkentin JD, Olson EN. Defining the regulatory networks for muscle development. Curr Opin Genet Dev 1996; 6:445 - 453
   PubMed Web of Science ®Google Scholar
• Weintraub H. The MyoD family and myogenesis: redundancy, networks and thresholds. Cell 1993; 75:1241 - 1244
   PubMed Web of Science ®Google Scholar
• Weintraub H, Tapscott SJ, Davis RL, Thayer MJ, Adam MA, Lassar AB, et al. Activation of musclespecific genes in pigment, nerve, fat, liver and fibroblast cell lines by forced expression of MyoD. Proc Natl Acad Sci USA 1989; 86:5434 - 5438
   PubMed Web of Science ®Google Scholar
• Gerber AN, Klesert TR, Bergstrom DA, Tapscott SJ. Two domains of MyoD mediate transcriptional activation of genes in repressive chromatin: a mechanism for lineage determination in myogenesis. Genes Dev 1997; 11:436 - 450
   PubMedGoogle Scholar
• Guasconi V, Puri PL. Chromatin: the interface between extrinsic cues and the epigenetic regulation of muscle regeneration. Trends Cell Biol 2009; 19:286 - 294
   PubMed Web of Science ®Google Scholar
• Seale P, Sabourin LA, Girgis-Gabardo A, Mansouri A, Gruss P, Rudnicki MA. Pax7 is required for the specification of myogenic satellite cells. Cell 2000; 102:777 - 786
   PubMed Web of Science ®Google Scholar
• Oustanina S, Hause G, Braun T. Pax7 directs postnatal renewal and propagation of myogenic satellite cells but not their specification. EMBO J 2004; 23:3430 - 3439
   PubMed Web of Science ®Google Scholar
• Lepper C, Conway SJ, Fan CM. Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements. Nature 2009; 460:627 - 631
   PubMed Web of Science ®Google Scholar
• Zammit PS, Relaix F, Nagata Y, Ruiz AP, Collins CA, Partridge TA, et al. Pax7 and myogenic progression in skeletal muscle satellite cells. J Cell Sci 2006; 119:1824 - 1832
   PubMed Web of Science ®Google Scholar
• Kuang S, Kuroda K, Le Grand F, Rudnicki MA. Asymmetric self-renewal and commitment of satellite stem cells in muscle. Cell 2007; 129:999 - 1010
   PubMed Web of Science ®Google Scholar
• Conboy IM, Rando TA. The regulation of Notch signaling controls satellite cell activation and cell fate determination in postnatal myogenesis. Dev Cell 2002; 3:397 - 409
   PubMed Web of Science ®Google Scholar
• Shinin V, Gayraud-Morel B, Gomes D, Tajbakhsh S. Asymmetric division and cosegregation of template DNA strands in adult muscle satellite cells. Nat Cell Biol 2006; 8:677 - 687
   PubMed Web of Science ®Google Scholar
• Fischle W, Wang Y, Allis CD. Histone and chromatin cross-talk. Curr Opin Cell Biol 2003; 15:172 - 183
   PubMed Web of Science ®Google Scholar
• Mal A, Sturniolo M, Schiltz RL, Ghosh MK, Harter ML. A role for histone deacetylase HDAC1 in modulating the transcriptional activity of MyoD: inhibition of the myogenic program. EMBO J 2001; 20:1739 - 1753
   PubMed Web of Science ®Google Scholar
• Puri PL, Iezzi S, Stiegler P, Chen TT, Schiltz RL, Muscat GE, et al. Class I histone deacetylases sequentially interact with MyoD and pRb during skeletal myogenesis. Mol Cell 2001; 8:885 - 897
   PubMed Web of Science ®Google Scholar
• McKinsey TA, Zhang CL, Lu J, Olson EN. Signaldependent nuclear export of a histone deacetylase regulates muscle differentiation. Nature 2000; 408:106 - 111
   PubMed Web of Science ®Google Scholar
• McKinsey TA, Zhang CL, Olson EN. Signaling chromatin to make muscle. Curr Opin Cell Biol 2002; 14:763 - 772
   PubMed Web of Science ®Google Scholar
• Sartorelli V, Puri PL. The link between chromatin structure, protein acetylation and cellular differentiation. Front Biosci 2001; 6:1024 - 1047
   Web of Science ®Google Scholar
• Zhang CL, McKinsey TA, Olson EN. Association of class II histone deacetylases with heterochromatin protein 1: potential role for histone methylation in control of muscle differentiation. Mol Cell Biol 2002; 22:7302 - 7312
   PubMed Web of Science ®Google Scholar
• Caretti G, Di Padova M, Micales B, Lyons GE, Sartorelli V. The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation. Genes Dev 2004; 18:2627 - 2638
   PubMed Web of Science ®Google Scholar
• Eckner R, Yao TP, Oldread E, Livingston DM. Interaction and functional collaboration of p300/CBP and bHLH proteins in muscle and B-cell differentiation. Genes Dev 1996; 10:2478 - 2490
   PubMed Web of Science ®Google Scholar
• Yuan W, Condorelli G, Caruso M, Felsani A, Giordano A. Human p300 protein is a coactivator for the transcription factor MyoD. J Biol Chem 1996; 271:9009 - 9013
   PubMed Web of Science ®Google Scholar
• Puri PL, Avantaggiati ML, Balsano C, Sang N, Graessmann A, Giordano A, et al. p300 is required for MyoD-dependent cell cycle arrest and muscle-specific gene transcription. EMBO J 1997; 16:369 - 383
   PubMed Web of Science ®Google Scholar
• Sartorelli V, Huang J, Hamamori Y, Kedes L. Molecular mechanisms of myogenic coactivation by p300: direct interaction with the activation domain of MyoD and with the MADS box of MEF2C. Mol Cell Biol 1997; 17:1010 - 1026
   PubMed Web of Science ®Google Scholar
• Puri PL, Sartorelli V, Yang XJ, Hamamori Y, Ogryzko VV, Howard BH, et al. Differential roles of p300 and PCAF acetyltransferases in muscle differentiation. Mol Cell 1997; 1:35 - 45
   PubMed Web of Science ®Google Scholar
• Chen SL, Loffler KA, Chen D, Stallcup MR, Muscat GE. The coactivator-associated arginine methyltransferase is necessary for muscle differentiation: CARM1 coactivates myocyte enhancer factor-2. J Biol Chem 2002; 277:4324 - 4333
   PubMed Web of Science ®Google Scholar
• Dacwag CS, Ohkawa Y, Pal S, Sif S, Imbalzano AN. The protein arginine methyltransferase Prmt5 is required for myogenesis because it facilitates ATPdependent chromatin remodeling. Mol Cell Biol 2007; 27:384 - 394
   PubMed Web of Science ®Google Scholar
• de la Serna IL, Carlson KA, Imbalzano AN. Mammalian SWI/SNF complexes promote MyoD-mediated muscle differentiation. Nat Genet 2001; 27:187 - 190
   PubMedGoogle Scholar
• Simone C, Forcales SV, Hill DA, Imbalzano AN, Latella L, Puri PL. p38 pathway targets SWI-SNF chromatin-remodeling complex to muscle-specific loci. Nat Genet 2004; 36:738 - 743
   PubMed Web of Science ®Google Scholar
• Rampalli S, Li L, Mak E, Ge K, Brand M, Tapscott SJ, et al. p38 MAPK signaling regulates recruitment of Ash2L-containing methyltransferase complexes to specific genes during differentiation. Nat Struct Mol Biol 2007; 14:1150 - 1156
   PubMed Web of Science ®Google Scholar
• de la Serna IL, Ohkawa Y, Imbalzano AN. Chromatin remodelling in mammalian differentiation: lessons from ATP-dependent remodellers. Nat Rev Genet 2006; 7:461 - 473
   PubMed Web of Science ®Google Scholar
• Martens JA, Winston F. Recent advances in understanding chromatin remodeling by Swi/Snf complexes. Curr Opin Genet Dev 2003; 13:136 - 142
   PubMed Web of Science ®Google Scholar
• Serra C, Palacios D, Mozzetta C, Forcales SV, Morantte I, Ripani M, et al. Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation. Mol Cell 2007; 28:200 - 213
   PubMed Web of Science ®Google Scholar
• Gillespie MA, Le Grand F, Scime A, Kuang S, von Maltzahn J, Seale V, et al. p38-{gamma~-dependent gene silencing restricts entry into the myogenic differentiation program. J Cell Biol 2009; 187:991 - 1005
   PubMed Web of Science ®Google Scholar
• Lassar AB, Paterson BM, Weintraub H. Transfection of a DNA locus that mediates the conversion of 10T1/2 fibroblasts to myoblasts. Cell 1986; 47:649 - 656
   PubMed Web of Science ®Google Scholar
• Lee H, Habas R, Abate-Shen C. MSX1 cooperates with histone H1b for inhibition of transcription and myogenesis. Science 2004; 304:1675 - 1678
   PubMed Web of Science ®Google Scholar
• Yokoyama S, Ito Y, Ueno-Kudoh H, Shimizu H, Uchibe K, Albini S, et al. A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58. Dev Cell 2009; 17:836 - 848
   PubMed Web of Science ®Google Scholar
• Ambros V. microRNAs: tiny regulators with great potential. Cell 2001; 107:823 - 826
   PubMed Web of Science ®Google Scholar
• Williams AH, Liu N, van Rooij E, Olson EN. MicroRNA control of muscle development and disease. Curr Opin Cell Biol 2009; 21:461 - 469
   PubMed Web of Science ®Google Scholar
• Bartel DP. MicroRNAs: genomics, biogenesis, mechanism and function. Cell 2004; 116:281 - 297
   PubMed Web of Science ®Google Scholar
• Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell 2009; 136:215 - 233
   PubMed Web of Science ®Google Scholar
• Stefani G, Slack FJ. Small non-coding RNAs in animal development. Nat Rev Mol Cell Biol 2008; 9:219 - 230
   PubMed Web of Science ®Google Scholar
• van Rooij E, Liu N, Olson EN. MicroRNAs flex their muscles. Trends Genet 2008; 24:159 - 166
   PubMed Web of Science ®Google Scholar
• Bernstein E, Kim SY, Carmell MA, Murchison EP, Alcorn H, Li MZ, et al. Dicer is essential for mouse development. Nat Genet 2003; 35:215 - 217
   PubMed Web of Science ®Google Scholar
• O’Rourke JR, Georges SA, Seay HR, Tapscott SJ, McManus MT, Goldhamer DJ, et al. Essential role for Dicer during skeletal muscle development. Dev Biol 2007; 311:359 - 368
   PubMed Web of Science ®Google Scholar
• Chen JF, Mandel EM, Thomson JM, Wu Q, Callis TE, Hammond SM, et al. The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation. Nat Genet 2006; 38:228 - 233
   PubMed Web of Science ®Google Scholar
• Liu N, Williams AH, Kim Y, McAnally J, Bezprozvannaya S, Sutherland LB, et al. An intragenic MEF2-dependent enhancer directs muscle-specific expression of microRNAs 1 and 133. Proc Natl Acad Sci USA 2007; 104:20844 - 20849
   PubMed Web of Science ®Google Scholar
• Rao PK, Kumar RM, Farkhondeh M, Baskerville S, Lodish HF. Myogenic factors that regulate expression of muscle-specific microRNAs. Proc Natl Acad Sci USA 2006; 103:8721 - 8726
   PubMed Web of Science ®Google Scholar
• Rosenberg MI, Georges SA, Asawachaicharn A, Analau E, Tapscott SJ. MyoD inhibits Fstl1 and Utrn expression by inducing transcription of miR-206. J Cell Biol 2006; 175:77 - 85
   PubMed Web of Science ®Google Scholar
• Mishima Y, Abreu-Goodger C, Staton AA, Stahlhut C, Shou C, Cheng C, et al. Zebrafish miR-1 and miR-133 shape muscle gene expression and regulate sarcomeric actin organization. Genes Dev 2009; 23:619 - 632
   PubMed Web of Science ®Google Scholar
• Juan AH, Kumar RM, Marx JG, Young RA, Sartorelli V. Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells. Mol Cell 2009; 36:61 - 74
   PubMed Web of Science ®Google Scholar
• Watanabe T, Sato T, Amano T, Kawamura Y, Kawamura N, Kawaguchi H, et al. Dnm3os, a non-coding RNA, is required for normal growth and skeletal development in mice. Dev Dyn 2008; 237:3738 - 3748
   PubMed Web of Science ®Google Scholar
• Wong CF, Tellam RL. MicroRNA-26a targets the histone methyltransferase Enhancer of Zeste homolog 2 during myogenesis. J Biol Chem 2008; 283:9836 - 9843
   PubMed Web of Science ®Google Scholar
• Wang H, Garzon R, Sun H, Ladner KJ, Singh R, Dahlman J, et al. NFkappaB-YY1-miR-29 regulatory circuitry in skeletal myogenesis and rhabdomyosarcoma. Cancer Cell 2008; 14:369 - 381
   PubMed Web of Science ®Google Scholar
• Kim HK, Lee YS, Sivaprasad U, Malhotra A, Dutta A. Muscle-specific microRNA miR-206 promotes muscle differentiation. J Cell Biol 2006; 174:677 - 687
   PubMed Web of Science ®Google Scholar
• Anderson C, Catoe H, Werner R. MIR-206 regulates connexin43 expression during skeletal muscle development. Nucleic Acids Res 2006; 34:5863 - 5871
   PubMed Web of Science ®Google Scholar
• Taulli R, Bersani F, Foglizzo V, Linari A, Vigna E, Ladanyi M, et al. The muscle-specific microRNA miR-206 blocks human rhabdomyosarcoma growth in xenotransplanted mice by promoting myogenic differentiation. J Clin Invest 2009; 119:2366 - 2378
   PubMed Web of Science ®Google Scholar
• Naguibneva I, Ameyar-Zazoua M, Polesskaya A, Ait-Si-Ali S, Groisman R, Souidi M, et al. The microRNA miR-181 targets the homeobox protein Hox-A11 during mammalian myoblast differentiation. Nat Cell Biol 2006; 8:278 - 284
   PubMed Web of Science ®Google Scholar
• Crist CG, Montarras D, Pallafacchina G, Rocancourt D, Cumano A, Conway SJ, et al. Muscle stem cell behavior is modified by microRNA-27 regulation of Pax3 expression. Proc Natl Acad Sci USA 2009; 13383 - 13387
   PubMed Web of Science ®Google Scholar