A. C. Mcpherron, A. M. Lawler, and S. J. Lee, Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member, Nature, vol.387, pp.83-90, 1997.

R. Kambadur, M. Sharma, T. P. Smith, and J. J. Bass, Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle, Genome Res, vol.7, pp.910-916, 1997.

L. Grobet, L. J. Martin, D. Poncelet, D. Pirottin, B. Brouwers et al., A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle, Nat Genet, vol.17, pp.71-74, 1997.
URL : https://hal.archives-ouvertes.fr/hal-02686447

L. Grobet, D. Poncelet, L. Royo, B. Brouwers, D. Pirottin et al., Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle, Mamm Genome, vol.9, pp.210-213, 1998.
URL : https://hal.archives-ouvertes.fr/hal-02695193

J. H. Holmes and C. R. Ashmore, A histochemical study of development of muscle fiber type and size in normal and "double muscled" cattle, Growth, vol.36, pp.351-372, 1972.

H. J. Swatland and N. M. Kieffer, Fetal development of the double muscled condition in cattle, J Anim Sci, vol.38, pp.752-757, 1974.

H. Gagnière, F. Ménissier, Y. Geay, and B. Picard, Influence of genotype on contractile protein differentiation in different bovine muscles during foetal life, Ann Zoot, vol.49, pp.1-19, 2000.

V. Deveaux, I. Cassar-malek, and P. Picard, Comparison of contractile characteristics of muscle from Holstein and Double-Muscled Belgian Blue foetuses, Comp Biochem Physiol, vol.131, pp.21-29, 2001.
URL : https://hal.archives-ouvertes.fr/hal-02674499

V. Deveaux, B. Picard, and J. Bouley, Cassar-Malek I: Location of myostatin expression during bovine myogenesis in vivo and in vitro, Reprod Nutr Dev, vol.43, pp.527-542, 2003.

A. J. Bailey, M. B. Enser, E. Dransfield, D. J. Restall, N. Avery et al., Muscle and adipose tissue from normal and double muscled cattle: collagen types, muscle fiber diameter, fat cell size and fatty acid composition and organoleptic properties. In Muscle hypertrophy of genetic origin and its use to improve, vol.1982, pp.178-204

K. R. Wagner, Muscle regeneration through myostatin inhibition, Curr Opin Rheumatol, vol.17, pp.720-724, 2005.

D. Joulia-ekaza and G. Cabello, Myostatin regulation of muscle development: Molecular basis, natural mutations, physiological aspects, Exp Cell Res, vol.312, p.345, 2006.

M. Thomas, B. Langley, C. Berry, M. Sharma, S. Kirk et al., Myostatin, a negative regulator of muscle growth, functions by inhibiting myoblast proliferation, J Biol Chem, vol.275, pp.40235-40243, 2000.

B. Picard, F. Depreux, and Y. Geay, Muscle differentiation of normal and double-muscled bovine foetal myoblasts in primary culture, Basic Appl Myol, vol.8, pp.197-203, 1998.
URL : https://hal.archives-ouvertes.fr/hal-02695390

R. Ríos, C. Carneiro, V. Arce, and J. Devesa, Myostatin is an inhibitor of myogenic differentiation

, Am J Physiol Cell Physiol, vol.282, pp.993-999, 2002.

B. Langley, M. Thomas, A. Bishop, M. Sharma, S. Gilmour et al., Myostatin Inhibits Myoblast Differentiation by Down-regulating MyoD Expression, J Biol Chem, vol.277, pp.49831-49840, 2002.

X. Zhu, S. Topouzis, L. F. Liang, and R. L. Stotish, Myostatin signaling through Smad2, Smad3 and Smad4 is regulated by the inhibitory Smad7 by a negative feedback mechanism, Cytokine, vol.26, pp.262-272, 2004.

B. Philip, Z. Lu, and Y. Gao, Regulation of GDF-8 signaling by the p38 MAPK, Cell Signalling, vol.17, pp.365-375, 2005.

D. Joulia, H. Bernardi, V. Garandel, F. Rabenoelina, B. Vernus et al., Mechanisms involved in the inhibition of myoblast proliferation and differentiation by myostatin, Exp Cell Res, vol.286, pp.263-275, 2003.
URL : https://hal.archives-ouvertes.fr/hal-02675798

J. Bouley, B. Meunier, C. Chambon, D. Smet, S. Hocquette et al., Proteomic analysis of bovine skeletal muscle hypertrophy, Proteomics, vol.5, pp.490-500, 2005.
URL : https://hal.archives-ouvertes.fr/hal-02680776

K. Sudre, C. Leroux, G. Piétu, I. Cassar-malek, E. Petit et al., Transcriptome analysis of two bovine muscles during ontogenesis, J Biochem, vol.133, pp.745-756, 2003.
URL : https://hal.archives-ouvertes.fr/hal-02682738

B. Picard, L. Lefaucheur, C. Berri, and M. J. Duclos, Muscle fibre ontogenesis in farm animal species, Reprod Nutr Dev, vol.42, pp.415-431, 2002.
URL : https://hal.archives-ouvertes.fr/hal-00900337

A. Everts-van-der-wind, D. M. Larkin, C. A. Green, J. S. Elliott, C. A. Olmstead et al., A highresolution whole-genome cattle-human comparative map reveals details of mammalian chromosome evolution, Proc Natl Acad Sci U S A, vol.102, pp.18526-18531, 2005.

E. Casas, J. W. Keele, S. D. Shackelford, M. Koohmaraie, T. S. Sonstegard et al., Association of the muscle hypertrophy locus with carcass traits in beef cattle, J Anim Sci, vol.76, pp.468-473, 1998.

C. A. Steelman, J. C. Recknor, D. Nettleton, and J. M. Reecy, Transcriptional profiling of myostatin-knockout mice implicates Wnt signaling in postnatal skeletal muscle growth and hypertrophy, FASEB J, vol.20, pp.580-582, 2006.

J. K. Potts, S. E. Echternkamp, T. P. Smith, and J. M. Reecy, Characterization of gene expression in double-muscled and normal-muscled bovine embryos, Anim Genet, vol.34, pp.438-444, 2003.

F. Verrecchia, E. F. Wagner, and A. Mauviel, Distinct involvement of the Jun-N-terminal kinase and NF-kappaB pathways in the repression of the human COL1A2 gene by TNF-alpha, EMBO Rep, vol.3, pp.1069-1074, 2002.
URL : https://hal.archives-ouvertes.fr/inserm-00147463

N. Karasseva, G. Tsika, J. J. Zhang, A. Mao, and X. , Tsika R: 1 binds multiple muscle MEF2 and A/T-rich elements during fast-to-slow skeletal muscle fiber type transitions, Mol Cell Biol, vol.23, pp.5143-5164, 2003.

A. P. Halestrap and D. Meredith, The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond, Pflueg Arch Eur J Physiol, vol.447, pp.619-628, 2004.

S. Girgenrath, K. Song, and L. Whittemore, Loss of myostatin expression alters fiber-type distribution and expression of myosine heavy chain isoforms in slow-and fast-type skeletal muscle, Muscle Nerve, vol.31, pp.34-40, 2005.

C. Ashmore, W. Parker, H. Stokes, and L. Doerr, Comparative aspects of muscle fibre types in fetuses of the normal and double muscled cattle, Growth, vol.38, pp.501-506, 1974.

S. C. Goetsch, T. J. Hawke, T. D. Gallardo, J. A. Richardson, and D. J. Garry, Transcriptional profiling and regulation of the extracellular matrix during muscle regeneration, Physiol Genomics, vol.14, pp.261-271, 2003.

J. R. Sanes, The basement membrane/basal lamina of skeletal muscle, J Biol Chem, vol.278, pp.12601-12604, 2003.

R. Hanset, The major gene of muscular hypertrophy in the Belgian Blue cattle breed, Breeding for disease resistance in farm animals, pp.467-478, 1991.

F. Ménissier, General survey of the effect of double muscling on cattle performance. In Muscle hypertrophy of genetic origin and its use to improve beef production Edited by: King JBW, Ménissier F. The Hague Martinus Nijhoff, vol.1982, pp.21-53

A. Listrat, B. Picard, and Y. Geay, Age-related changes and location of type I, III, IV, V and VI collagens during development of four foetal skeletal muscles of double-muscled and normal bovine animals, Tissue Cell, vol.31, pp.17-27, 1999.
URL : https://hal.archives-ouvertes.fr/hal-02688751

K. Rautavuoma, K. Takaluoma, R. Sormunen, J. Myllyharju, K. I. Kivirikko et al., Premature aggregation of type IV collagen and early lethality in lysylhydroxylase 3 null mice, Proc Natl Acad Sci, vol.101, pp.14120-14125, 2004.

A. Schaffler, A. Ehling, E. Neumann, H. Herfarth, I. Tarner et al., Genomic organization, chromosomal localization and adipocytic expression of the murine gene for CORS-26 (collagenous repeat-containing sequence of 26 kDa protein), Biochim Biophys Acta, vol.1628, pp.64-70, 2003.

J. Lin, H. B. Arnold, M. A. Della-fera, M. J. Azain, D. L. Hartzell et al., Myostatin knockout in mice increases myogenesis and decreases adipogenesis, Biochem Biophys Res Commun, vol.291, pp.701-716, 2002.

J. N. Artaza, S. Bhasin, T. R. Magee, S. Reisz-porszasz, R. Shen et al., Myostatin inhibits myogenesis and promotes adipogenesis in C3H 10T(1/2) mesenchymal multipotent cells, Endocrinology, vol.146, pp.3547-3557, 2005.

I. Barnola, J. Hocquette, I. Cassar-malek, C. Jurie, G. Gentès et al., Adipocyte fatty acid-binding protein expression and mitochondrial activity as indicators of Intramuscular fat content in young bulls, Indicators of milk and beef quality Edited by: Hocquette J-F, Gigli S. EAAP Publication 112, pp.419-424, 2005.
URL : https://hal.archives-ouvertes.fr/hal-02763158

D. S. Cianzo, D. G. Topel, G. B. Whitehurst, D. C. Beitz, and H. L. Self, Adipose tissue growth and cellularity: changes in bovine adipocyte and number, J Anim Sci, vol.60, pp.970-976, 1985.

H. Gagnière, B. Picard, and Y. Geay, Contractile differentiation of foetal cattle muscles: intermuscular variability, Reprod Nutr Dev, vol.39, pp.637-655, 1999.

. Cardioserve, IFR 26 de Nantes

A. Brazma, P. Hingamp, J. Quackenbush, G. Sherlock, P. Spellman et al.,

T. , G. P. Holstege, F. Kim, I. F. Markowitz, V. Matese et al., Minimum information about a microarray experiment (MIAME) -toward standards for microarray data, Nature Genet, vol.29, pp.365-371, 2001.

G. Entrez and . Profiles,

L. Meur, N. Lamirault, G. Bihouée, A. Steenman, M. Bédrine-ferran et al., A dynamic, web-accessible resource to process raw microarray scan data into consolidated gene expression values: importance of replication, Nucleic Acids Res, vol.32, pp.5349-5358, 2004.

V. G. Tusher, R. Tibshirani, and G. Chu, Significance analysis of microarrays applied to the ionizing radiation response, Proc Natl Acad Sci, vol.98, pp.5116-5120, 2001.

G. Didier, P. Brezellec, R. E. Henaut, and A. , GeneANOVA -gene expression analysis of variance, Bioinformatics, vol.18, pp.490-491, 2002.
URL : https://hal.archives-ouvertes.fr/hal-01614111

A. Sturn, J. Quackenbush, and Z. Trajanoski, Genesis: cluster analysis of microarray data, Bioinformatics, vol.18, pp.207-208, 2002.

, Babelomics

F. Al-shahrour, P. Minguez, J. M. Vaquerizas, L. Conde, and J. Dopazo, Babelomics: a suite of web-tools for functional annotation and analysis of group of genes in high-throughput experiments, Nucleic Acids Res, vol.33, pp.460-464, 2005.

G. Portal,