[Accili D., Arden K.C. (2004). FoxOs at the crossroads of cellular review metabolism, differentiation, and transformation. Cell, 117: 421–426.]Search in Google Scholar
[Andreote A.P.D., Rosario M.F., Ledur M.C., Jorge E.C., Sonstegard T.S., Matukumalli L., Coutinho L.L. (2014). Identification and characterization of microRNAs expressed in chicken skeletal muscle. Genet. Mol. Res., 13: 1465–1479; https://doi.org/10.4238/2014.March.6.5.10.4238/2014..6.5]Open DOISearch in Google Scholar
[Baquero-Perez B., Kuchipudi S.V., Nelli R.K., Chang K.C. (2012). A simplified but robust method for the isolation of avian and mammalian muscle satellite cells. BMC Cell Biol. 13, 16; https://doi.org/10.1186/1471-2121-13-16.10.1186/1471-2121-13-16343259722720831]Open DOISearch in Google Scholar
[Bassel-Duby R., Olson E.N. (2006). Signaling pathways in skeletal muscle remodeling. Annu. Rev. Biochem.,75: 19–37; https://doi.org/10.1146/annurev.biochem.75.103004.142622.10.1146/annurev.biochem.75.103004.14262216756483]Open DOISearch in Google Scholar
[Berkes C.A., Tapscott S.J. (2005). MyoD and the transcriptional control of myogenesis. Semin. Cell Dev. Biol., 16: 585–595; https://doi.org/10.1016/j.semcdb.2005.07.006.10.1016/j.semcdb.2005.07.00616099183]Open DOISearch in Google Scholar
[Bodine S.C., Stitt T.N., Gonzalez M., Kline W.O., Stover G.L., Bauerlein R., Zlotchenko E., Scrimgeour A., Lawrence J.C., Glass D.J., Yancopoulos G.D. (2001). Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo. Nat. Cell Biol., 3: 1014–1019; https://doi.org/10.1038/ncb1101-1014.10.1038/ncb1101-101411715023]Open DOISearch in Google Scholar
[Boutz P.L., Chawla G., Stoilov P., Black D.L. (2007). MicroRNAs regulate the expression of the alternative splicing factor nPTB during muscle development. Genes Dev., 21: 71–84; https://doi.org/10.1101/gad.1500707.10.1101/gad.1500707175990217210790]Open DOISearch in Google Scholar
[Braun T., Gautel M. (2011). Transcriptional mechanisms regulating skeletal muscle differentiation, growth and homeostasis. Nat. Rev. Mol. Cell Biol., 12: 349–361; https://doi.org/10.1038/nrm3118.10.1038/nrm311821602905]Open DOISearch in Google Scholar
[Buckingham M. (2006). Myogenic progenitor cells and skeletal myogenesis in vertebrates. Curr. Opin. Genet. Dev.; https://doi.org/10.1016/j.gde.2006.08.008.10.1016/j.gde.2006.08.00816930987]Open DOISearch in Google Scholar
[Buechner J., Tømte E., Haug B.H., Henriksen J.R., Løkke C., Flægstad T., Einvik C. (2011). Tumour-suppressor microRNAs let-7 and mir-101 target the proto-oncogene MYCN and inhibit cell proliferation in MYCN-amplified neuroblastoma. Br. J. Cancer, 105: 296–303; https://doi.org/10.1038/bjc.2011.220.10.1038/bjc.2011.220314280321654684]Open DOISearch in Google Scholar
[Burattini S., Ferri R., Battistelli M., Curci R., Luchetti F., Falcieri E. (2004). C2C12 murine myoblasts as a model of skeletal muscle development: Morpho-functional characterization. Eur. J. Histochem., 48: 223–233.]Search in Google Scholar
[Cardinalli B., Castellani L., Fasanaro P., Basso A., Alemà S., Martelli F., Falcone G. (2009). Microrna-221 and microrna-222 modulate differentiation and maturation of skeletal muscle cells. PLoS One, 4; https://doi.org/10.1371/journal.pone.0007607.10.1371/journal.pone.0007607276261419859555]Search in Google Scholar
[Castigliego L., Armani A., Grifoni G., Rosati R., Mazzi M., Gianfaldoni D., Guidi A. (2010). Effects of growth hormone treatment on the expression of somatotropic axis genes in the skeletal muscle of lactating Holstein cows. Domest. Anim. Endocrinol., 39: 40–53; https://doi.org/10.1016/j.domaniend.2010.02.00110.1016/j.domaniend.2010.02.00120399067]Open DOISearch in Google Scholar
[Chen B., Xu J., He X., Xu H., Li G., Du H., Nie Q., Zhang X. (2015). A genome-wide mRNA screen and functional analysis reveal FOXO3 as a candidate gene for chicken growth. PLoS One, 10: 1–22; https://doi.org/10.1371/journal.pone.0137087.10.1371/journal.pone.0137087456932826366565]Open DOISearch in Google Scholar
[Chen J.F., Mandel E.M., Thomson J.M., Wu Q., Callis T.E., Hammond S.M., Conlon F.L., Wang D.Z. (2006). The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation. Nat. Genet., 38: 228–233; https://doi.org/10.1038/ng1725.10.1038/ng1725253857616380711]Open DOISearch in Google Scholar
[Chen J.F., Tao Y., Li J., Deng Z., Yan Z., Xiao X., Wang D.Z. (2010) microRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7. J. Cell Biol., 190: 867–879; https://doi.org/10.1083/jcb.200911036.10.1083/jcb.200911036293556520819939]Open DOISearch in Google Scholar
[Chen L., Li Y.S., Cui J., Ning J.N., Wang G.S., Qian G.S., Lu K.Z., Yi B. (2014). MiR-206 controls the phenotypic modulation of pulmonary arterial smooth muscle cells induced by serum from rats with Hepatopulmonary syndrome by regulating the target gene, Annexin A2. Cell. Physiol. Biochem., 34: 1768–1779; https://doi.org/10.1159/000366377.10.1159/00036637725427750]Open DOISearch in Google Scholar
[Chung F.W., Tellam R.L. (2008). MicroRNA-26a targets the histone methyltransferase enhancer of zeste homolog 2 during myogenesis. J. Biol. Chem., 283: 9836–9843; https://doi.org/10.1074/jbc.M709614200.10.1074/jbc.709614200]Open DOISearch in Google Scholar
[Clop A., Marcq F., Takeda H., Pirottin D., Tordoir X., Bibé B., Bouix J., Caiment F., Elsen J.M., Eychenne F., Larzul C., Laville E., Meish F., Milenkovic D., Tobin J., Charlier C., Georges M. (2006). A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep. Nat. Genet., 38: 813–818; https://doi.org/10.1038/ng1810.10.1038/ng181016751773]Open DOISearch in Google Scholar
[Crippa S., Cassano M., Messina G., Galli D., Galvez B.G., Curk T., Altomare C., Ronzoni F., Toelen J., Gijsbers R., Debyser Z., Janssens S., Zupan B., Zaza A., Cossu G., Sampaolesi M. (2011). miR669a and miR669q prevent skeletal muscle differentiation in postnatal cardiac progenitors. J. Cell Biol., 193: 1197–1212; https://doi.org/10.1083/jcb.201011099.10.1083/jcb.201011099321634021708977]Open DOISearch in Google Scholar
[Crist C.G., Montarras D., Pallafacchina G., Rocancourt D., Cumano A., Conway S.J., Buckingham M. (2009). Muscle stem cell behavior is modified by microRNA-27 regulation of Pax3 expression. Proc. Natl. Acad. Sci., 106: 13383–13387; https://doi.org/10.1073/pnas.0900210106.10.1073/pnas.0900210106272638119666532]Open DOISearch in Google Scholar
[Cui T.X., Schwartz J., Piwien-Pilipuk G., Lanning N., Rathore M., LaPensee C.R., Calinescu A.-A., Lin G., Jin H., Qin Z.S., Carter-Su C., Streeter C. (2011). C/EBPβ mediates growth hormone-regulated expression of multiple target genes. Mol. Endocrinol., 25: 681–693; https://doi.org/10.1210/me.2010-0232.10.1210/me.2010-0232306308621292824]Open DOISearch in Google Scholar
[Cutting A.D., Bannister S.C., Doran T.J., Sinclair A.H., Tizard M.V.L., Smith C.A. (2012). The potential role of microRNAs in regulating gonadal sex differentiation in the chicken embryo. Chromosom. Res., 20: 201–213; https://doi.org/10.1007/s10577-011-9263-y.10.1007/s10577-011-9263-y22161018]Open DOISearch in Google Scholar
[Darnell D.K., Kaur S., Stanislaw S., Konieczka J.K., Yatskievych T.A., Antin P.B. (2006). MicroRNA expression during chick embryo development. Dev. Dyn., 235: 3156–3165; https://doi.org/10.1002/dvdy.20956.10.1002/dvdy.2095617013880]Open DOISearch in Google Scholar
[De Mario A., Quintana-Cabrera R., Martinvalet D., Giacomello M. (2017). (Neuro)degenerated Mitochondria-ER contacts. Biochem. Biophys. Res. Commun., 483: 1096–1109; https://doi.org/10.1016/j.bbrc.2016.07.056.10.1016/j.bbrc.2016.07.05627416756]Open DOISearch in Google Scholar
[Dey B.K., Gagan J., Yan Z., Dutta A. (2012). miR-26a is required for skeletal muscle differentiation and regeneration in mice. Genes Dev., 26: 2180–2191; https://doi.org/10.1101/gad.198085.112.10.1101/gad.198085.112346573923028144]Open DOISearch in Google Scholar
[Draeger A., Babiychuk E.B., Schaller J., Palstra R.-J.T.S., Kämpfer U. (2002). Annexin VI participates in the formation of a reversible, membrane-cytoskeleton complex in smooth muscle cells. J. Biol. Chem., 274: 35191–3519; https://doi.org/10.1074/jbc.274.49.35191.10.1074/jbc.274.49.3519110575003]Search in Google Scholar
[Dupont J., Holzenberger M. (2003). Biology of insulin-like growth factors in development. Birth Defects Res. Part C: Embryo Today: Rev.; https://doi.org/10.1002/bdrc.10022.10.1002/bdrc.1002214745968]Open DOISearch in Google Scholar
[Egerman M.A., Glass D.J. (2014). Signaling pathways controlling skeletal muscle mass. Crit. Rev. Biochem. Mol. Biol., 49: 59–68; https://doi.org/10.3109/10409238.2013.857291.10.3109/10409238.2013.857291391308324237131]Open DOISearch in Google Scholar
[Elia L., Contu R., Quintavalle M., Varrone F., Chimenti C., Russo M.A., Cimino V., De Marinis L., Frustaci A., Catalucci D., Condorelli G. (2009). Reciprocal regulation of microRNA-1 and insulin-like growth factor-1 signal transduction cascade in cardiac and skeletal muscle in physiological and pathological conditions. Circulation, 120: 2377–2385; https://doi.org/10.1161/CIRCULATIONAHA.109.879429.10.1161/CIRCULATIONAHA.109.879429282565619933931]Open DOISearch in Google Scholar
[Eun J.L., Baek M., Gusev Y., Brackett D.J., Nuovo G.J., Schmittgen T.D. (2008). Systematic evaluation of microRNA processing patterns in tissues, cell lines, and tumors. RNA, 14: 35–42; https://doi.org/10.1261/rna.804508.10.1261/rna.804508215102718025253]Open DOISearch in Google Scholar
[Feng Y., Cao J.H., Li X.Y., Zhao S.H. (2011). Inhibition of miR-214 expression represses proliferation and differentiation of C2C12 myoblasts. Cell Biochem. Funct., 29: 378–383; https://doi.org/10.1002/cbf.1760.10.1002/cbf.176021520152]Open DOISearch in Google Scholar
[Feng Y., Niu L.L., Wei W., Zhang W.Y., Li X.Y., Cao J.H., Zhao S.H. (2013). A feedback circuit between miR-133 and the ERK1/2 pathway involving an exquisite mechanism for regulating myoblast proliferation and differentiation. Cell Death Dis., 4: 934; https://doi.org/10.1038/cddis.2013.462.10.1038/cddis.2013.462384733824287695]Open DOISearch in Google Scholar
[Flynt A.S., Li N., Thatcher E.J., Solnica-Krezel L., Patton J.G. (2007). Zebrafish miR-214 modulates Hedgehog signaling to specify muscle cell fate. Nat. Genet., 39: 259–263; https://doi.org/10.1038/ng1953.10.1038/ng1953398279917220889]Open DOISearch in Google Scholar
[Gan W., He H., Li L. (2016). Molecular cloning, characterisation and functional analysis of the duck Forkhead box O3 (FOXO3) gene. Br. Poult. Sci., 57: 143–150; https://doi.org/10.1080/00071668.2015.113550.10.1080/00071668.2015.113550]Open DOISearch in Google Scholar
[Ge Y., Sun Y., Chen J. (2011). IGF-II is regulated by microRNA-125b in skeletal myogenesis. J. Cell Biol., 192: 69–81; https://doi.org/10.1083/jcb.201007165.10.1083/jcb.201007165301954721200031]Open DOISearch in Google Scholar
[Glazov E.A., Cottee P.A., Barris W.C., Moore R.J., Dalrymple B.P., Tizard M.L. (2008). A microRNA catalog of the developing chicken embryo identified by a deep sequencing approach. Genome Res., 18: 957–964; https://doi.org/10.1101/gr.074740.107.10.1101/gr.074740.107241316318469162]Open DOISearch in Google Scholar
[Goettsch C., Rauner M., Pacyna N., Hempel U., Bornstein S.R., Hofbauer L.C. (2011). MiR-125b regulates calcification of vascular smooth muscle cells. Am. J. Pathol., 179: 1594–1600; https://doi.org/10.1016/j.ajpath.2011.06.016.10.1016/j.ajpath.2011.06.016318138321806957]Open DOISearch in Google Scholar
[Grifone R., Demignon J., Giordani J., Niro C., Souil E., Bertin F., Laclef C., Xu P.X., Maire P. (2007). Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo. Dev. Biol., 302: 602–616; https://doi.org/10.1016/j.ydbio.2006.08.059.10.1016/j.ydbio.2006.08.05917098221]Open DOISearch in Google Scholar
[Gu L., Xu T., Huang W., Xie M., Sun S., Hou S. (2014). Identification and profiling of microRNAs in the embryonic breast muscle of Pekin duck. PLoS One, 9: 1–13; https://doi.org/10.1371/journal.pone.0086150.10.1371/journal.pone.0086150390048024465928]Open DOISearch in Google Scholar
[Gu Z. (2004). The single nucleotide polymorphisms of the chicken myostatin gene are associated with skeletal muscle and adipose growth. Sci. China Ser. C 47, 25; https://doi.org/10.1360/02yc0201.10.1360/02yc020115382673]Open DOISearch in Google Scholar
[Guo C.S., Degnin C., Fiddler T.A., Stauffer D., Thayer M.J. (2003). Regulation of MyoD activity and muscle cell differentiation by MDM2, pRb, and Sp1. J. Biol. Chem., 278: 22615–22622; https://doi.org/10.1074/jbc.M301943200.10.1074/jbc.301943200]Open DOISearch in Google Scholar
[Hache R.J.G., Wiper-Bergeron N., Salem H.A., Wu D., Tomlinson J.J. (2007). Glucocorticoid-stimulated preadipocyte differentiation is mediated through acetylation of C/EBPbeta by GCN5. Proc. Natl. Acad. Sci., 104: 2703–2708; https://doi.org/10.1073/pnas.0607378104.10.1073/pnas.0607378104181524517301242]Open DOISearch in Google Scholar
[Hadjiargyrou M., Lombardo F., Zhao S., Ahrens W., Joo J., Ahn H., Jurman M., White D.W., Rubin C.T. (2002). Transcriptional profiling of bone regeneration. Insight into the molecular complexity of wound repair. J. Biol. Chem., 277: 30177–30182; https://doi.org/10.1074/jbc.M203171200.10.1074/jbc.203171200]Open DOISearch in Google Scholar
[Hak K.K., Yong S.L., Sivaprasad U., Malhotra A., Dutta A. (2006). Muscle-specific microRNA miR-206 promotes muscle differentiation. J. Cell Biol., 174: 677–687; https://doi.org/10.1083/jcb.200603008.10.1083/jcb.200603008206431116923828]Open DOISearch in Google Scholar
[Hamburger V., Hamilton H.L. (1951). A series of normal stages in the development of the chick embryo. J. Morphol., 88: 49–92; https://doi.org/10.1002/jmor.1050880104.10.1002/jmor.1050880104]Open DOISearch in Google Scholar
[Harding R.L., Velleman S.G. (2016). MicroRNA regulation of myogenic satellite cell proliferation and differentiation. Mol. Cell. Biochem., 412: 181–195; https://doi.org/10.1007/s11010-015-2625-6.10.1007/s11010-015-2625-626715133]Open DOISearch in Google Scholar
[Harris L.K., Westwood M. (2012). Biology and significance of signalling pathways activated by IGF-II. Growth Factors; https://doi.org/10.3109/08977194.2011.640325.10.3109/08977194.2011.64032522136428]Open DOISearch in Google Scholar
[Hennebry A., Berry C., Siriett V., O ’Callaghan P., Chau L., Watson T., Sharma M., Kambadur R. (2008). Myostatin regulates fiber-type composition of skeletal muscle by regulating MEF2 and MyoD gene expression. AJP Cell Physiol., 296: 525–534; https://doi.org/10.1152/ajpcell.00259.2007.10.1152/ajpcell.00259.200719129464]Open DOISearch in Google Scholar
[Hicks J.A., Tembhurne P., Liu H.C. (2008). MicroRNA expression in chicken embryos. Poultry Sci., 87: 2335–2343; https://doi.org/10.3382/ps.2008-00114.10.3382/ps.2008-0011418931185]Open DOISearch in Google Scholar
[Hicks J.A., Trakooljul N., Liu H.-C. (2010). Discovery of chicken microRNAs associated with lipogenesis and cell proliferation. Physiol. Genomics, 41: 185–193; https://doi.org/10.1152/physiolgenomics.00156.2009.10.1152/physiolgenomics.00156.200920103699]Open DOISearch in Google Scholar
[Hillier L.W., Miller W., Birney E., Warren W., Hardison R.C., Ponting C.P., Bork P., Burt D.W., Groenen M.A.M., Delany M.E., Dodgson J.B. (2004). Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Nature, 432: 695–716; https://doi.org/10.1038/nature03154.10.1038/03154]Open DOISearch in Google Scholar
[Hirai H., Verma M., Watanabe S., Tastad C., Asakura Y., Asakura A. (2010). MyoD regulates apoptosis of myoblasts through microRNA-mediated down-regulation of Pax3. J. Cell Biol., 191: 347–365; https://doi.org/10.1083/jcb.201006025.10.1083/jcb.201006025295847920956382]Open DOISearch in Google Scholar
[Hu R., Pan W., Fedulov A. V., Jester W., Jones M.R., Weiss S.T., Panettieri R.A., Tantisira K., Lu Q. (2014). MicroRNA-10a controls airway smooth muscle cell proliferation via direct targeting of the PI3 kinase pathway. FASEB J., 28: 2347–2357; https://doi.org/10.1096/fj.13-247247.10.1096/fj.13-247247398684124522205]Search in Google Scholar
[Huang H., Xie C., Sun X., Ritchie R.P., Zhang J., Eugene Chen Y. (2010). miR-10a contributes to retinoid acid-induced smooth muscle cell differentiation. J. Biol. Chem., 285: 9383–9389; https://doi.org/10.1074/jbc.M109.095612.10.1074/jbc.M109.095612284318720118242]Search in Google Scholar
[Huang M.B., Xu H., Xie S.J., Zhou H., Qu L.H. (2011). Insulin-like growth factor-1 receptor is regulated by microRNA-133 during skeletal myogenesis. PLoS One, 6; https://doi.org/10.1371/journal.pone.0029173.10.1371/journal.pone.0029173324064022195016]Open DOISearch in Google Scholar
[Huang T.H., Zhu M.J., Li X.Y., Zhao S.H. (2008). Discovery of porcine microRNAs and profiling from skeletal muscle tissues during development. PLoS One, 3; https://doi.org/10.1371/journal.pone.0003225.10.1371/journal.pone.0003225252894418795099]Open DOISearch in Google Scholar
[Hunter R.B., Kandarian S.C. (2004). Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy. J. Clin. Invest., 114: 1504–1511; https://doi.org/10.1172/JCI200421696.10.1172/JCI200421696]Open DOISearch in Google Scholar
[Ishibashi J., Perry R.L., Asakura A., Rudnicki M.A. (2005). MyoD induces myogenic differentiation through cooperation of its NH2- and COOH-terminal regions. J. Cell Biol., 171: 471–482; https://doi.org/10.1083/jcb.200502101.10.1083/jcb.200502101217126916275751]Open DOISearch in Google Scholar
[Jebessa E., Ouyang H., Abdalla B.A., Li Z. (2017). Characterization of miRNA and their target gene during chicken embryo skeletal muscle development. Oncotarget, 9: 17309–17324; https://doi.org/10.18632/oncotarget.22457.10.18632/oncotarget.22457591511829707110]Search in Google Scholar
[Jia X., Lin H., Abdalla B.A., Nie Q. (2016). Characterization of miR-206 promoter and its association with birthweight in chicken. Int. J. Mol. Sci. 17, 559; https://doi.org/10.3390/ijms17040559.10.3390/ijms17040559484901527089330]Open DOISearch in Google Scholar
[Juan A.H., Kumar R.M., Marx J.G., Young R.A., Sartorelli V. (2009). Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells. Mol. Cell., 36: 61–74; https://doi.org/10.1016/j.molcel.2009.08.008.10.1016/j.molcel.2009.08.008276124519818710]Open DOISearch in Google Scholar
[Junqing L., Shuisheng H., Wei H., Junying Y., Wenwu W. (2011). Polymorphisms in the myostatin gene and their association with growth and carcass traits in duck. African J. Biotechnol., 10: 11309–11312; https://doi.org/10.5897/AJB11.512.10.5897/AJB11.512]Search in Google Scholar
[Kablar B., Rudnicki M.A. (2000). Skeletal muscle development in the mouse embryo. Histol. Histopathol.; https://doi.org/10.14670/HH-15.649.]Search in Google Scholar
[Khanna N., Ge Y., Chen J. (2014). MicroRNA-146b promotes myogenic differentiation and modulates multiple gene targets in muscle cells. PLoS One, 9; https://doi.org/10.1371/journal.pone.0100657.10.1371/journal.pone.0100657]Open DOISearch in Google Scholar
[Khatri B., Seo D., Shouse S., Pan J.H., Hudson N.J., Kim J.K., Bottje W., Kong B.C. (2018). MicroRNA profiling associated with muscle growth in modern broilers compared to an unselected chicken breed. BMC Genomics, 19: 1–10; https://doi.org/10.1186/s12864-018-5061-7.10.1186/s12864-018-5061-7]Open DOISearch in Google Scholar
[Koomkrong N., Theerawatanasirikul S., Boonkaewwan C., Jaturasitha S., Kayan A. (2015). Breed-related number and size of muscle fibres and their response to carcass quality in chickens. Ital. J. Anim. Sci., 14: 638–642; https://doi.org/10.4081/ijas.2015.4145.10.4081/ijas.2015.4145]Open DOISearch in Google Scholar
[Koutsoulidou A., Mastroyiannopoulos N.P., Furling D., Uney J.B., Phylactou L.A. (2011). Expression of miR-1, miR-133a, miR-133b and miR-206 increases during development of human skeletal muscle. BMC Dev. Biol.,11: 1–9; https://doi.org/10.1186/1471-213X-11-34.10.1186/1471-213X-11-34]Open DOISearch in Google Scholar
[Lagos-Quintana M., Rauhut R., Yalcin A., Meyer J., Lendeckel W., Tuschl T. (2002). Identification of tissue-specific MicroRNAs from mouse. Curr. Biol., 12: 735–739; https://doi.org/10.1016/S0960-9822(02)00809-6.10.1016/S0960-9822(02)00809-6]Open DOISearch in Google Scholar
[Lawlor M.W., De Chene E.T., Roumm E., Geggel A.S., Moghadaszadeh B., Beggs A.H. (2010). Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion. Hum. Mutat., 31: 176–183; https://doi.org/10.1002/humu.21157.10.1002/humu.21157281519919953533]Open DOISearch in Google Scholar
[Li T., Wu R., Zhang Y., Zhu D. (2011). A systematic analysis of the skeletal muscle miRNA transcriptome of chicken varieties with divergent skeletal muscle growth identifies novel miRNAs and differentially expressed miRNAs. BMC Genomics, 12; https://doi.org/10.1186/1471-2164-12-186.10.1186/1471-2164-12-186310718421486491]Open DOISearch in Google Scholar
[Li Z., Abdalla B.A., Zheng M., He X., Cai B., Han P., Ouyang H., Chen B., Nie Q., Zhang X. (2018). Systematic transcriptome-wide analysis of mRNA–miRNA interactions reveals the involvement of miR-142-5p and its target (FOXO3) in skeletal muscle growth in chickens. Mol. Genet. Genomics, 293: 69–80; https://doi.org/10.1007/s00438-017-1364-7.10.1007/s00438-017-1364-728866851]Open DOISearch in Google Scholar
[Liang Y., Ridzon D., Wong L., Chen C. (2007). Characterization of microRNA expression profiles in normal human tissues. BMC Genomics, 8: 166; https://doi.org/10.1186/1471-2164-8-166.10.1186/1471-2164-8-166190420317565689]Search in Google Scholar
[Liu C., Gersch R.P., Hawke T.J., Hadjiargyrou M. (2010). Silencing of Mustn1 inhibits myogenic fusion and differentiation. Am. J. Physiol. Physiol., 298: 1100–1108; https://doi.org/10.1152/ajpcell.00553.2009.10.1152/ajpcell.00553.2009286739320130207]Open DOISearch in Google Scholar
[Liu J., Luo X.J., Xiong A.W., Zhang Z., Di Yue S., Zhu M.S., Cheng S.Y. (2010). MicroRNA-214 promotes myogenic differentiation by facilitating exit from mitosis via down-regulation of proto-oncogene N-ras. J. Biol. Chem.; https://doi.org/10.1074/jbc.M110.115824.10.1074/jbc.M110.115824292409820534588]Open DOISearch in Google Scholar
[Liu N., Bezprozvannaya S., Shelton J.M., Frisard M.I., Hulver M.W., McMillan R.P., Wu Y., Voelker K.A., Grange R.W., Richardson J.A., Bassel-Duby R., Olson E.N. (2011). Mice lacking microRNA 133a develop dynamin 2-dependent centronuclear myopathy. J. Clin. Invest., 121: 3258–3268; https://doi.org/10.1172/JCI46267.10.1172/JCI46267314873721737882]Open DOISearch in Google Scholar
[Liu X., Cheng Y., Zhang S., Lin Y., Yang J., Zhangr C. (2009). A necessary role of miR-221 and miR-222 in vascular smooth muscle cell prolife ation and neointimal hyperplasia. Circ. Res., 104: 476–486; https://doi.org/10.1161/CIRCRESAHA.108.185363.10.1161/CIRCRESAHA.108.185363272829019150885]Open DOISearch in Google Scholar
[Lu L., Zhou L., Chen E.Z., Sun K., Jiang P., Wang L., Su X., Sun H., Wang H. (2012). A novel YY1-miR-1 regulatory circuit in skeletal myogenesis revealed by genome-wide prediction of YY1-miRNA network. PLoS One 7. https://doi.org/10.1371/journal.pone.0027596.10.1371/journal.pone.0027596327107622319554]Open DOISearch in Google Scholar
[Luo W., Nie Q., Zhang X. (2013). MicroRNAs involved in skeletal muscle differentiation. J. Genet. Genomics, 40: 107–116; https://doi.org/10.1016/j.jgg.2013.02.002.10.1016/j.jgg.2013.02.00223522383]Open DOISearch in Google Scholar
[McCarthy J.J. (2008). MicroRNA-206: The skeletal muscle-specific myomiR. Biochim. Biophys. Acta – Gene Regul. Mech., 1779: 682–691; https://doi.org/10.1016/j.bbagrm.2008.03.001.10.1016/j.bbagrm.2008.03.001265639418381085]Open DOISearch in Google Scholar
[McCarthy J.J., Esser K.A. (2006). MicroRNA-1 and microRNA-133a expression are decreased during skeletal muscle hypertrophy. J. Appl. Physiol., 102: 306–313; https://doi.org/10.1152/japplphysiol.00932.2006.10.1152/japplphysiol.00932.200617008435]Open DOISearch in Google Scholar
[McDaneld T.G., Smith T.P.L., Doumit M.E., Miles J.R., Coutinho L.L., Sonstegard T.S., Matukumalli L.K., Nonneman D.J., Wiedmann R.T. (2009). MicroRNA transcriptome profiles during swine skeletal muscle development. BMC Genomics, 10: 77; https://doi.org/10.1186/1471-2164-10-77.10.1186/1471-2164-10-77264674719208255]Search in Google Scholar
[Mendias C.L., Bakhurin K.I., Faulkner J.A. (2008). Tendons of myostatin-deficient mice are small, brittle, and hypocellular. Proc. Natl. Acad. Sci., 105: 388–393; https://doi.org/10.1073/pnas.0707069105.10.1073/pnas.0707069105222422218162552]Open DOISearch in Google Scholar
[Moss F.P., Leblond C.P. (1971). Satellite cells as the source of nuclei in muscles of growing rats. Anat. Rec., 170: 421–435; https://doi.org/10.1002/ar.1091700405.10.1002/ar.10917004055118594]Open DOISearch in Google Scholar
[Naguibneva I., Ameyar-Zazoua M., Polesskaya A., Ait-Si-Ali S., Groisman R., Souidi M., Cuvellier S., Harel-Bellan A. (2006). The microRNA miR-181 targets the homeobox protein Hox-A11 during mammalian myoblast differentiation. Nat. Cell Biol., 8: 278–284; https://doi.org/10.1038/ncb1373.10.1038/ncb137316489342]Search in Google Scholar
[O’Rourke J.R., Mc Anally J., Moresi V., Gerard R.D., Sutherland L.B., Olson E.N., Richardson J.A., Small E.M. (2010). Regulation of PI3-kinase/Akt signaling by muscle-enriched microRNA-486. Proc. Natl. Acad. Sci., 107: 4218–4223; https://doi.org/10.1073/pnas.1000300107.10.1073/pnas.1000300107284009920142475]Open DOISearch in Google Scholar
[Potthoff M.J., Olson E.N. (2007). MEF2: a central regulator of diverse developmental programs. Development, 134: 4131–4140; https://doi.org/10.1242/dev.008367.10.1242/dev.00836717959722]Open DOISearch in Google Scholar
[Rathjen T., Pais H., Sweetman D., Moulton V., Munsterberg A., Dalmay T. (2009). High throughput sequencing of microRNAs in chicken somites. FEBS Lett., 583: 1422–1426; https://doi.org/10.1016/j.febslet.2009.03.048.10.1016/j.febslet.2009.03.04819328789]Open DOISearch in Google Scholar
[Richards M.P., Poch S.M., Mc Murtry J.P. (2005). Expression of insulin-like growth factor system genes in liver and brain tissue during embryonic and post-hatch development of the turkey. Comp. Biochem. Physiol. – A Mol. Integr. Physiol., 141: 76–86; https://doi.org/10.1016/j.cbpb.2005.04.006.10.1016/j.cbpb.2005.04.00615905111]Open DOISearch in Google Scholar
[Rivas D.A., Lessard S.J., Rice N.P., Lustgarten M.S., So K., Goodyear L.J., Parnell L.D., Fielding R.A. (2014). Diminished skeletal muscle microRNA expression with aging is associated with attenuated muscle plasticity and inhibition of IGF-1 signaling. FASEB J., 28: 4133–4147; https://doi.org/10.1096/fj.14-254490.10.1096/fj.14-254490505831824928197]Open DOISearch in Google Scholar
[Saccone V., Puri P.L. (2010). Epigenetic regulation of skeletal myogenesis. Organogenesis, 6: 48–53; https://doi.org/10.4161/org.6.1.11293.10.4161/org.6.1.11293286174320592865]Open DOISearch in Google Scholar
[Schellander K., Holker M., Hossain M.M., Tesfaye D., Salilew-Wondim D., Cinar M.U., Kocamis H., Mohammadi-Sangcheshmeh A. (2013). Expression of microRNA and microRNA processing machinery genes during early quail (Coturnix japonica) embryo development. Poultry Sci., 92: 787–797; https://doi.org/10.3382/ps.2012-02691.10.3382/ps.2012-0269123436530]Open DOISearch in Google Scholar
[Shen H., McElhinny A.S., Cao Y., Gao P., Liu J., Bronson R., Griffin J.D., Wu L. (2006). The Notch coactivator, MAML1, functions as a novel coactivator for MEF2C-mediated transcription and is required for normal myogenesis. Genes Dev., 20: 675–688; https://doi.org/10.1101/gad.1383706.10.1101/gad.1383706141328416510869]Open DOISearch in Google Scholar
[Song C.L., Liu H.H., Kou J., Lv L., Li L., Wang W.X., Wang J.W. (2012). Expression profile of insulin-like growth factor system genes in muscle tissues during the postnatal development growth stage in ducks. Genet. Mol. Res., 12: 4500–4514; https://doi.org/10.4238/2013.May.6.3.10.4238/2013..6.3]Open DOISearch in Google Scholar
[Sumariwalla V.M., Klein W.H. (2001). Similar myogenic functions for myogenin and MRF4 but not MyoD in differentiated murine embryonic stem cells. Genesis, 30: 239–249; https://doi.org/10.1002/gene.1070.10.1002/gene.107011536430]Open DOISearch in Google Scholar
[Sun Q., Zhang Y., Yang G., Chen X., Zhang Y., Cao G., Wang J., Sun Y., Zhang P., Fan M., Shao N., Yang X. (2008). Transforming growth factor-β-regulated miR-24 promotes skeletal muscle differentiation. Nucleic Acids Res., 36: 2690–2699; https://doi.org/10.1093/nar/gkn032.10.1093/nar/gkn032237743418353861]Open DOISearch in Google Scholar
[Sun Y., Ge Y., Drnevich J., Zhao Y., Band M., Chen J. (2010). Mammalian target of rapamycin regulates miRNA-1 and follistatin in skeletal myogenesis. J. Cell Biol., 189: 1157–1169; https://doi.org/10.1083/jcb.200912093.10.1083/jcb.200912093289444820566686]Open DOISearch in Google Scholar
[Sweetman D., Goljanek K., Rathjen T., Oustanina S., Braun T., Dalmay T., Münsterberg A. (2008). Specific requirements of MRFs for the expression of muscle specific microRNAs, miR-1, miR-206 and miR-133. Dev. Biol., 321: 491–499; https://doi.org/10.1016/j.ydbio.2008.06.019.10.1016/j.ydbio.2008.06.01918619954]Open DOISearch in Google Scholar
[Takaya T., Ono K., Kawamura T., Takanabe R., Kaichi S., Morimoto T., Wada H., Kita T., Shimatsu A., Hasegawa K. (2009). MicroRNA-1 and MicroRNA-133 in spontaneous myocardial differentiation of mouse embryonic stem cells. Circ. J., 73: 1492–1497; https://doi.org/10.1253/circj.CJ-08-1032.10.1253/circj.CJ-08-1032]Open DOISearch in Google Scholar
[Townley-Tilson W.H.D., Callis T.E., Wang D. (2010). MicroRNAs 1, 133, and 206: Critical factors of skeletal and cardiac muscle development, function, and disease. Int. J. Biochem. Cell Biol.; https://doi.org/10.1016/j.biocel.2009.03.002.10.1016/j.biocel.2009.03.002290432220619221]Open DOISearch in Google Scholar
[van der Horst A., Burgering B.M.T., (2007). Stressing the role of FoxO proteins in lifespan and disease. Nat. Rev. Mol. Cell Biol., 8: 440–450; https://doi.org/10.1038/nrm2190.10.1038/nrm219017522590]Search in Google Scholar
[van Rooij E., Sutherland L.B., Qi X., Richardson J.A., Hill J., Olson E.N. (2007). Control of stress-dependent cardiac growth and gene expression by a microRNA. Science, 80: 575–579; https://doi.org/10.1126/science.1139089.10.1126/.1139089]Open DOISearch in Google Scholar
[van Rooij E., Liu N., Olson E.N. (2008). MicroRNAs flex their muscles. Trends Genet., 24: 159–166; https://doi.org/10.1016/j.tig.2008.01.007.10.1016/j.tig.2008.01.00718325627]Open DOISearch in Google Scholar
[Velleman S.G., Nestor K.E., Coy C.S., Harford I., Anthony N.B. (2010). Effect of posthatch feed restriction on broiler breast muscle development and muscle transcriptional regulatory factor gene and heparan sulfate proteoglycan expression. Int. J. Poult. Sci., 9: 417–425; https://doi.org/10.3923/ijps.2010.417.425.10.3923/ijps.2010.417.425]Open DOISearch in Google Scholar
[Wang H., Li X., Liu H., Sun L., Zhang R., Li L., Wangding M., Wang J. (2016). Six1 induces protein synthesis signaling expression in duck myoblasts mainly via up-regulation of mTOR. Genet. Mol. Biol., 39: 151–161; https://doi.org/10.1590/1678-4685-GMB-2015-0075.10.1590/1678-4685-GMB-2015-0075480738227007909]Open DOISearch in Google Scholar
[Wang S., Aurora A.B., Johnson B.A., Qi X., McAnally J., Hill J.A., Richardson J.A., Bassel-Duby R., Olson E.N. (2008). The endothelial-specific MicroRNA miR-126 governs vascular integrity and angiogenesis. Dev. Cell, 15: 261–271; https://doi.org/10.1016/j.devcel.2008.07.002.10.1016/j.devcel.2008.07.002268576318694565]Open DOISearch in Google Scholar
[Wang X.H., Hu Z., Klein J.D., Zhang L., Fang F., Mitch W.E. (2011). Decreased miR-29 suppresses myogenesis in CKD. J. Am. Soc. Nephrol., 22: 2068–2076; https://doi.org/10.1681/ASN.2010121278.10.1681/ASN.2010121278323178321965375]Open DOISearch in Google Scholar
[White R.B., Biérinx A., Gnocchi V.F., Zammit P.S. (2010). Dynamics of muscle fibre growth during postnatal mouse development, BMC Developmental Biology, 10.10.1186/1471-213X-10-21283699020175910]Search in Google Scholar
[Wood W.M., Etemad S., Yamamoto M., Goldhamer D.J. (2013). MyoD-expressing progenitors are essential for skeletal myogenesis and satellite cell development. Dev. Biol., 384: 114–127; https://doi.org/10.1016/j.ydbio.2013.09.012.10.1016/j.ydbio.2013.09.012383890124055173]Open DOISearch in Google Scholar
[Wu N., Gu T., Lu L., Cao Z., Song Q., Wang Z., Zhang Y., Chang G., Xu Q., Chen G. (2019). Roles of miRNA-1 and miRNA-133 in the proliferation and differentiation of myoblasts in duck skeletal muscle. J. Cell. Physiol., 234: 3490–3499; https://doi.org/10.1002/jcp.26857.10.1002/jcp.2685730471101]Open DOISearch in Google Scholar
[Xu T., Huang W., Zhang X., Ye B., Zhou H., Hou S. (2012). Identification and characterization of genes related to the development of breast muscles in Pekin duck. Mol. Biol. Rep., 39: 7647–7655; https://doi.org/10.1007/s11033-012-1599-7.10.1007/s11033-012-1599-722451153]Open DOISearch in Google Scholar
[Xu T.S., Gu L.H., Zhang X.H., Ye B.G., Liu X.L., Hou S.S. (2013 a). Characterization of myostatin gene (MSTN) of Pekin duck and the association of its polymorphism with breast muscle traits. Genet. Mol. Res., 12: 3166–3177; https://doi.org/10.4238/2013.February.28.18.10.4238/2013.February.28.1823479163]Open DOISearch in Google Scholar
[Xu T.S., Gu L.H., Zhang X.H., Huang W., Ye B.G., Liu X.L., Hou S.S. (2013 b). IGF-1 and FoxO3 expression profiles and developmental differences of breast and leg muscle in Pekin ducks during postnatal stages. J. Anim. Vet. Adv., 12: 852–858.]Search in Google Scholar
[Xu T.S., Gu L.H., Sun Y., Zhang X.H., Ye B.G., Liu X.L., Hou S.S. (2015). Characterization of MUSTN1 gene and its relationship with skeletal muscle development at postnatal stages in Pekin ducks. Genet. Mol. Res., 14: 4448–4460; https://doi.org/10.4238/2015.May.4.2.10.4238/2015..4.2]Open DOISearch in Google Scholar
[Xu T.S., Gu L.H., Huang W., Xia W.L., Zhang Y.S., Zhang Y.G., Rong G., Schachtschneider K., Hou S.S. (2017). Gene expression profiling in Pekin duck embryonic breast muscle. PLoS One, 12: 1–18; https://doi.org/10.1371/journal.pone.0174612.10.1371/journal.pone.0174612541748328472139]Open DOISearch in Google Scholar
[Yaffe D., Saxel O. (1977). A myogenic cell line with altered serum requirements for differentiation. Differentiation, 7: 159–166; https://doi.org/10.1111/j.1432-0436.1977.tb01507.x.10.1111/j.1432-0436.1977.tb01507.x558123]Open DOISearch in Google Scholar
[Yin H., Pasut A., Soleimani V.D., Bentzinger C.F., Antoun G., Thorn S., Seale P., Fernando P., Van Ijcken W., Grosveld F., Dekemp R.A., Boushel R., Harper M.E., Rudnicki M.A. (2013). MicroRNA-133 controls brown adipose determination in skeletal muscle satellite cells by targeting Prdm16. Cell Metab., 17: 210–224; https://doi.org/10.1016/j.cmet.2013.01.004.10.1016/j.cmet.2013.01.004364165723395168]Open DOISearch in Google Scholar
[Yin H., Zhang S., Gilbert E.R., Siegel P.B., Zhu Q., Wong E.A. (2014). Expression profiles of muscle genes in postnatal skeletal muscle in lines of chickens divergently selected for high and low body weight. Poultry Sci., 93: 147–154; https://doi.org/10.3382/ps.2013-03612.10.3382/ps.2013-0361224570434]Open DOISearch in Google Scholar
[Zhang J., Ying Z.Z., Tang Z.L., Long L.Q., Li K. (2012). MicroRNA-148a promotes myogenic differentiation by targeting the ROCK1 gene. J. Biol. Chem. 287: 21093–21101; https://doi.org/10.1074/jbc.M111.330381.10.1074/jbc.M111.330381337553222547064]Open DOISearch in Google Scholar
[Zhao Y., Samal E., Srivastava D. (2005). Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis. Nature, 436: 214–220; https://doi.org/10.1038/nature03817.10.1038/03817]Open DOISearch in Google Scholar
[Zhao Y., Hou Y., Zhang K., Yuan B., Peng X. (2017). Identification of differentially expressed miRNAs through high-throughput sequencing in the chicken lung in response to Mycoplasma gallisepticum HS. Comp. Biochem. Physiol. – Part D Genomics Proteomics, 22: 146–156; https://doi.org/10.1016/j.cbd.2017.04.004.10.1016/j.cbd.2017.04.00428433919]Open DOISearch in Google Scholar
[Zhu C., Song W., Tao Z., Liu H., Xu W., Zhang S., Li H. (2017). Deep RNA sequencing of pectoralis muscle transcriptomes during late-term embryonic to neonatal development in indigenous Chinese duck breeds. PLoS One, 12: 1–18; https://doi.org/10.1371/journal.pone.0180403.10.1371/journal.pone.0180403554242728771592]Open DOISearch in Google Scholar