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Advances in research on the prenatal development of skeletal muscle in animals in relation to the quality of muscle-based food. II – Genetic factors related to animal performance and advances in methodology

Published online by Cambridge University Press:  05 January 2011

C. Rehfeldt ,
M. F. W. Te Pas ,
K. Wimmers ,
J. M. Brameld ,
P. M. Nissen ,
C. Berri ,
L. M. P. Valente ,
D. M. Power ,
B. Picard  and
N. C. Stickland
...Show all authors
C. Rehfeldt*
Affiliation:
Research Units Muscle Biology and Growth/Molecular Biology, Leibniz Institute for Farm Animals (FBN), Wilhelm-Stahl-Allee, D-18196 Dummerstorf, Germany
M. F. W. Te Pas
Affiliation:
Animal Breeding and Genomics Centre, Wageningen UR Livestock Research, PO Box 65, AB Lelystad, The Netherlands
K. Wimmers
Affiliation:
Research Units Muscle Biology and Growth/Molecular Biology, Leibniz Institute for Farm Animals (FBN), Wilhelm-Stahl-Allee, D-18196 Dummerstorf, Germany
J. M. Brameld
Affiliation:
Division of Nutritional Sciences, University of Nottingham, School of Biosciences, Sutton Bonington Campus, Loughborough, Leics. LE12 5RD, UK
P. M. Nissen
Affiliation:
Faculty of Agricultural Sciences, Department of Food Science, Aarhus University, Blichers Allé 20, PO Box 50, DK-8830 Tjele, Denmark
C. Berri
Affiliation:
INRA, UR83 Recherches Avicoles, 37380 Nouzilly, France
L. M. P. Valente
Affiliation:
Centre of Marine and Environmental Research (CIMAR/CIIMAR) and Institute of Biomedical Sciences Abel Salazar (ICBAS), University of Porto, Rua dos Bragas 289, 4050-123 Porto, Portugal
D. M. Power
Affiliation:
Comparative and Molecular Endocrinology Group, CCMAR, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
B. Picard
Affiliation:
INRA, UR1213 Herbivores, Centre de Recherche de Clermont-Ferrand/Theix, 63122 Saint-Genès-Champanelle, France
N. C. Stickland
Affiliation:
Department of Veterinary Basic Sciences, The Royal Veterinary College, Royal College Street, London NW1 0TU, UK
N. Oksbjerg
Affiliation:
Faculty of Agricultural Sciences, Department of Food Science, Aarhus University, Blichers Allé 20, PO Box 50, DK-8830 Tjele, Denmark
*
†E-mail: [email protected]
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Abstract

Selective breeding is an effective tool to improve livestock. Several selection experiments have been conducted to study direct selection responses as well as correlated responses in traits of skeletal muscle growth and function. Moreover, comparisons of domestic with wild-type species and of extreme breeds provide information on the genetic background of the skeletal muscle phenotype. Structural muscular components that differed with increasing distance in lean growth or meat quality in mammals were found to be myofibre number, myofibre size, proportions of fibre types as well as the numbers and proportions of secondary and primary fibres. Furthermore, markers of satellite cell proliferation, metabolic enzyme activities, glycogen and fat contents, the expression of myosin heavy chain isoforms, of activated AMPKα and other proteins in skeletal muscle tissue and circulating IGF1 and IGF-binding proteins have been identified to be involved in selection responses observed in pigs, cattle and/or chicken. The use of molecular methods for selective breeding of fish has only recently been adopted in aquaculture and studies of the genetic basis of growth and flesh quality traits are scarce. Some of the molecular markers of muscle structure/metabolism in livestock have also been identified in fish, but so far no studies have linked them with selection response. Genome scans have been applied to identify genomic regions exhibiting quantitative trait loci that control traits of interest, for example, muscle structure and meat quality in pigs and growth rate in chicken. As another approach, polymorphisms in candidate genes reveal the relationship between genetic variation and target traits. Thus, in large-scale studies with pigs’ associations of polymorphisms in the HMGA2, CA3, EPOR, NME1 and TTN genes with traits of carcass and meat quality were detected. Other studies revealed the significance of mutations in the IGF2 and RYR1 genes for carcass lean and muscle fibre traits in pigs. Mutations in the myostatin (MSTN) gene in fish were also examined. Advances in research of the genetic and environmental control of traits related to meat quality and growth have been made by the application of holistic ‘omics’ techniques that studied the whole muscle-specific genome, transcriptome and proteome in relation to muscle and meat traits, the development of new methods for muscle fibre typing and the adaptation of biophysical measures to develop parameters of muscle fibre traits as well as the application of in vitro studies. Finally, future research priorities in the field are defined.

Keywords

farm animalfishskeletal muscleanimal performancegenetic effects
Type
Review
Information
animal , Volume 5 , Issue 5 , 04 April 2011 , pp. 718 - 730
Copyright
Copyright © The Animal Consortium 2011

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Footnotes

*

Authoring on behalf of all members of the COST action 925: http://www.agrsci.dk/costaction925/index.html

References

Archives of Animal Breeding 2005. Special Issue, vol. 48, 1–150.Google Scholar
Archives of Animal Breeding 2006. Special Issue, vol. 49, 1–154.Google Scholar
Archives of Animal Breeding 2007. Special Issue, vol. 50, 1–98.Google Scholar
Archives of Animal Breeding 2008. Special Issue 1, vol. 51, 1–91.CrossRefGoogle Scholar
Ashmore, CR, Tompkins, G, Doerr, L 1972. Postnatal development of muscle fiber types in domestic animals. Journal of Animal Science 34, 37–41.CrossRefGoogle ScholarPubMed
Andersen, NK, Ravn, LS, Guy, JH, Edwards, SA, Harrison, AP 2008. Postnatal changes in electromyographic signals during piglet growth, and in relation to muscle fibre types. Livestock Science 115, 301–312.CrossRefGoogle Scholar
Bai, Q, McGillivray, C, da Costa, N, Dornan, S, Evans, G, Stear, MJ, Chang, KC 2003. Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles. BMC Genomics 4, 8.CrossRefGoogle ScholarPubMed
Beccavin, C, Chevalier, B, Cogburn, LA, Simon, J, Duclos, MJ 2001. Insulin-like growth factors and body growth in chickens divergently selected for high or low growth rate. Journal of Endocrinology 168, 297–306.CrossRefGoogle ScholarPubMed
Bee, G, Deruy, JY 2008. Birth weight affects muscle fiber size and myosin heavy-chain isoform gene expression in the longissimus muscle of slaughter pigs. Proceedings of the Society of Nutrition Physiology 17, 112.Google Scholar
Bee, G, Solomon, MB, Czerwinski, SM, Long, C, Pursel, VG 1999. Correlation between histochemically assessed fiber type distribution and isomyosin and myosin heavy chain content in porcine skeletal muscles. Journal of Animal Science 77, 2104–2111.CrossRefGoogle ScholarPubMed
Bérard, J, Kreuzer, M, Écolan, P, Lefaucheur, L, Bee, G 2008. Effect of foetus weight at day 70 of gestation on muscle fiber number, myosin heavy chain isoform expression and proteomic pattern in three porcine muscles. A preliminary study. In Globalisierung und Klimawandel: Verändern sie die Tierernährung in der Schweiz? Tagungsbericht, Schriftenreihe aus dem INW 30, 120–123.Google Scholar
Bernard, C, Cassar-Malek, I, Le Cunff, M, Dubroeucq, H, Renand, G, Hocquette, J-F 2007. New indicators of beef sensory quality revealed by expression of specific genes. Journal of Agricultural and Food Chemistry 55, 5229–5237.CrossRefGoogle ScholarPubMed
Berri, C, Godet, E, Haj Hattab, N, Duclos, MJ 2006. Growth and differentiation of the chicken Pectoralis major muscle: effect of genotype and early nutrition. Archives of Animal Breeding 49 (Special Issue), 31–32.Google Scholar
Berri, C, Le Bihan-Duval, E, Debut, M, Sante-Lhoutellier, V, Baéza, E, Gigaud, V, Jego, Y, Duclos, MJ 2007. Consequence of muscle hypertrophy on characteristics of Pectoralis major muscle and breast meat quality of broiler chickens. Journal of Animal Science 85, 2005–2011.CrossRefGoogle ScholarPubMed
Berri, C, Le Bihan-Duval, E, Baéza, E, Chartrin, P, Picgirard, L, Jehl, N, Quentin, M, Picard, M, Duclos, MJ 2005. Further processing characteristics of breast and leg meat from fast-, medium and slow-growing commercial chickens. Animal Research 54, 123–134.CrossRefGoogle Scholar
Bouley, J, Chambon, C, Picard, B 2004. Mapping of bovine skeletal muscle proteins using two-dimensional gel electrophoresis and mass spectrometry. Proteomics 4, 1811–1824.CrossRefGoogle ScholarPubMed
Bouley, J, Meunier, B, Chambon, C, De Smet, S, Hocquette, JF, Picard, B 2005. Proteomic analysis of bovine skeletal muscle hypertrophy. Proteomics 5, 490–500.CrossRefGoogle ScholarPubMed
Brooke, MH, Kaiser, KK 1970. Muscle fiber types: how many and what kind? Archives of Neurology 23, 369–379.CrossRefGoogle ScholarPubMed
Bünger, L, Ott, G, Varga, L, Schlote, W, Rehfeldt, C, Williams, JL, Hill, WG 2004. Marker-assisted introgression of the Compact mutant myostatin allele into a mouse line with extreme growth – effects on body composition and muscularity. Genetic Research 84, 161–173.CrossRefGoogle ScholarPubMed
Cagnazzo, M, Te Pas, MFW, Priem, J, de Wit, A, Pool, MH, Davoli, R, Russo, V 2006. Comparison of prenatal muscle tissue expression profiles of two pig breeds differing in muscle characteristics. Journal of Animal Science 84, 1–10.CrossRefGoogle ScholarPubMed
Canario, AVM, Bargelloni, L, Volckaert, F, Houston, RD, Massault, C, Guiguen, Y 2008. Genomics toolbox for farmed fish. Reviews in Fisheries Science 16, 3–15.CrossRefGoogle Scholar
Cassar-Malek, I, Passelaigue, F, Bernard, C, Léger, J, Hocquette, JF 2007. Target genes of myostatin loss-of-function in muscles of late bovine fetuses. BMC Genomics 8, 63.CrossRefGoogle ScholarPubMed
Castillo, J, Codina, M, Martinez, ML, Navarro, I, Gutierrez, J 2004. Metabolic and mitogenic effects of IGF-I and insulin on muscle cells of rainbow trout. American Journal of Physiology-Regulatory Integrative and Comparative Physiology 286, R935–941.CrossRefGoogle ScholarPubMed
Castillo, J, Ammendrup-Johnsen, I, Codina, M, Navarro, I, Gutierrez, J 2006. IGF-I and insulin receptor signal transduction in trout muscle cells. American Journal of Physiology – Regulatory Integrative and Comparative Physiology 290, R1683–R1690.CrossRefGoogle ScholarPubMed
Cerisuelo, A, Sala, R, Nürnberg, G, Baucells, M, Rehfeldt, C 2007. How many muscle samples are required to obtain reliable estimations of muscle fibre characteristics from pig longissimus muscle? Meat Science 76, 583–587.CrossRefGoogle ScholarPubMed
Chang, KC, Fernandes, K 1997. Developmental expression and 5′ cloning of the porcine 2x and 2b myosin heavy chain genes. DNA and Cell Biology 16, 1429–1437.CrossRefGoogle ScholarPubMed
Chantry-Darmon, C, Urien, C, Hayes, H, Bertaud, M, Chadi-Taourit, S, Chardon, P, Vaiman, D, Rogel-Gaillard, C 2005. Construction of a cytogenetically anchored microsatellite map in rabbit. Mammalian Genome 16, 442–459.CrossRefGoogle ScholarPubMed
Chaze, T, Bouley, J, Chambon, C, Barboiron, C, Picard, B 2006. Mapping of alkaline proteins in bovine skeletal muscle. Proteomics 6, 2571–2575.CrossRefGoogle ScholarPubMed
Chaze, T, Meunier, B, Chambon, C, Jurie, C, Picard, B 2008. In vivo proteome dynamics during early bovine myogenesis. Proteomics 8, 4236–4248.CrossRefGoogle ScholarPubMed
Chelh, I, Meunier, B, Picard, B, Reecy, JM, Chevalier, C, Hocquette, J-F, Cassar-Malek, I 2009. Molecular profiles of quadriceps muscle in myostatin-null mice reveal PI3K and apoptotic pathways as myostatin targets. BMC Genomics 10, 196.CrossRefGoogle ScholarPubMed
Circa, AV, Eknath, AE, Taduan, AG 1995. Genetic improvement of farmed tilapias: the growth performance of the GIFT strain of Nile tilapia (Oreochromis niloticus) in rice-fish environments. Aquaculture 137, 329–330.CrossRefGoogle Scholar
Codina, M, de la Serrana, DG, Sanchez-Gurmaches, J, Montserrat, N, Chistyakova, O, Navarro, I, Gutierrez, J 2008. Metabolic and mitogenic effects of IGF-II in rainbow trout (Oncorhynchus mykiss) myocytes in culture and the role of IGF-II in the PI3K/Akt and MAPK signalling pathways. General and Comparative Endocrinology 157, 116–124.CrossRefGoogle ScholarPubMed
Cogburn, LA, Wang, X, Carre, W, Rejto, L, Aggrey, SE, Duclos, MJ, Simon, J, Porter, TE 2004. Functional genomics in chickens: development of integrated-systems microarrays for transcriptional profiling and discovery of regulatory pathways. Comparative and Functional Genomics 5, 253–261.CrossRefGoogle ScholarPubMed
Cogburn, LA, Porter, TE, Duclos, MJ, Simon, J, Burgess, S, Zhu, JJ, Cheng, H, Dodgson, JB, Burnside, J 2007. Functional genomics of the chicken: a model organism. Poultry Science 86, 2059–2094.CrossRefGoogle Scholar
Da Costa, N, Blackley, R, Alzuherri, H, Chang, KC 2002. Quantifying the temporospatial expression of postnatal porcine skeletal myosin heavy chain genes. Journal of Histochemistry and Cytochemistry 50, 353–364.CrossRefGoogle ScholarPubMed
Demars, J, Riquet, J, Sanchez, MP, Billon, Y, Hocquette, JF, Lebret, B, Iannuccelli, N, Bidanel, JP, Milan, D, Gondret, F 2007. Metabolic and histochemical characteristics of fat and muscle tissues in homozygous or heterozygous pigs for the body composition QTL located on chromosome 7. Physiological Genomics 30, 232–241.CrossRefGoogle ScholarPubMed
De-Santis, C, Jerry, DR 2007. Candidate growth genes in finfish – where should we be looking? Aquaculture 272, 22–38.CrossRefGoogle Scholar
Deveaux, V, Picard, B, Bouley, J, Cassar-Malek, I 2003. Location of myostatin expression during bovine myogenesis in vivo and in vitro. Reproduction Nutrition Development 43, 527–542.CrossRefGoogle ScholarPubMed
Duclos, MJ, Berri, C, Hattab, NJ 2005. Selection for growth rate alters the expression of rapid myosin heavy chain isoforms in chicken breast muscle. Archives of Animal Breeding 48 (Special Issue), 76.Google Scholar
Duclos, M, Berri, C, Le Bihan-Duval, E 2007. Muscle growth and meat quality. Journal of Applied Poultry Research 16, 107–112.CrossRefGoogle Scholar
Duclos, MJ, Molette, C, Guernec, A, Rémignon, H, Berri, C 2006. Cellular aspects of breast muscle development in chickens with high or low growth rate. Archives of Animal Breeding 49 (Special Issue), 147–151.Google Scholar
Duclos, MJ, Chevalier, B, Remignon, H, Ricard, FH, Goddard, C, Simon, J 1996. Divergent selection for high or low growth rate modifies the response of muscle cells to serum or insulin-like growth factor-I in vitro. Growth Regulation 6, 176–184.Google ScholarPubMed
Ernst, CW, Rilington, VD, Raney, NE, Yao, J, Sipkovsky, SS, Saama, PM, Tempelman, RJ, Coussens, PM 2002. Use of cDNA microarrays to detect differentially expressed genes in developing pig skeletal muscle. Abstracts for the Plant, Animal & Microbe Genomes X Conference, San Diego, CA, USA, 702pp.Google Scholar
Fiedler, I, Dietl, G, Rehfeldt, C, Wegner, J, Ender, K 2004. Muscle fibre traits as additional selection criteria for muscle growth and meat quality in pig – results of a simulated selection. Journal of Animal Breeding and Genetics 121, 331–344.CrossRefGoogle Scholar
Gardan, D, Gondret, F, Van den Maagdenberg, K, Buys, N, De Smet, S, Louveau, I 2008. Lipid metabolism and cellular features of skeletal muscle and subcutaneous adipose tissue in pigs differing in IGF-II genotype. Domestic Animal Endocrinology 34, 45–53.CrossRefGoogle ScholarPubMed
Gil, M, Delday, MI, Gispert, M, Font i Furnols, M, Maltin, CM, Plastow, GS, Klont, R, Sosnicki, AA, Carrión, D 2008. Relationships between biochemical characteristics and meat quality of longissimus thoracis and semimembranosus muscles in five porcine lines. Meat Science 3, 927–933.CrossRefGoogle Scholar
Gjedrem, T 2000. Genetic improvement of cold-water fish species. Aquaculture Research 31, 25–33.CrossRefGoogle Scholar
Gjoen, HM, Bentsen, HB 1997. Past, present, and future of genetic improvement in salmon aquaculture. ICES Journal of Marine Science 54, 1009–1014.CrossRefGoogle Scholar
Goddard, C, Wilkie, RS, Dunn, IC 1988. The relationship between insulin-like growth factor-1, growth hormone, thyroid hormones and insulin in chickens selected for growth. Domestic Animal Endocrinology 5, 165–176.CrossRefGoogle ScholarPubMed
Gondret, F, Larzul, C, Combes, S, de Rochambeau, H 2005. Carcass composition, bone mechanical properties, and meat quality traits in relation to growth rate in rabbits. Journal of Animal Science 83, 1526–1535.CrossRefGoogle ScholarPubMed
Graziotti, GH, Ríos, CM, Rivero, JL 2001. Evidence for three fast myosin heavy chain isoforms in type II skeletal muscle fibers in the adult Llama (Lama glama). Journal of Histochemistry and Cytochemistry 49, 1033–1044.CrossRefGoogle ScholarPubMed
Guernec, A, Berri, C, Chevalier, B, Wacrenier-Céré, N, Le Bihan-Duval, E, Duclos, MJ 2003. Muscle development, insulin-like growth factor-I and myostatin mRNA levels in chickens selected for increased breast muscle yield. Growth Hormone and IGF Research 13, 8–18.CrossRefGoogle ScholarPubMed
Harrison, AP, Latorre, R, Dauncey, MJ 1997. Postnatal development and differentiation of myofibres in functionally diverse porcine skeletal muscles. Reproduction and Fertility Development 9, 731–740.CrossRefGoogle ScholarPubMed
Hemmings, K, Parr, T, Buttery, P, Brameld, J 2008a. Development and evaluation of a real-time PCR method for determining skeletal muscle fibre type composition in sheep. Proceedings of the British Society for Animal Science, 47.Google Scholar
Hemmings, K, Parr, T, Buttery, P, Brameld, J 2008b. Development of a real-time PCR method for determining skeletal muscle fibre type composition in sheep. Archives of Animal Breeding 51 (Special Issue 1), 30.Google Scholar
Henckel, P, Oksbjerg, N, Erlandsen, E, Barton-Gade, P, Bejerholm, C 1997. Histo- and biochemical characteristics of the Longissimus dorsi muscle in pigs and their relationships to performance and meat quality. Meat Science 47, 311–321.CrossRefGoogle ScholarPubMed
Hurley, MS, Flux, C, Salter, AM, Brameld, JM 2006. Effects of fatty acids on skeletal muscle cell differentiation in vitro. British Journal of Nutrition 95, 623–630.CrossRefGoogle ScholarPubMed
Kalbe, C, Mau, M, Rehfeldt, C 2008. Developmental changes and the impact of isoflavones on mRNA expression of IGF-I receptor, EGF receptor and related growth factors in porcine skeletal muscle cell cultures. Growth Hormone & IGF Research 18, 424–433.CrossRefGoogle ScholarPubMed
Kalbe, C, Mau, M, Wollenhaupt, K, Rehfeldt, C 2007. Evidence for estrogen receptor α and β expression in skeletal muscle of pigs. Histochemistry and Cell Biology 127, 95–107.CrossRefGoogle ScholarPubMed
Knibb, W 2000. Genetic improvement of marine fish – which method for industry? Aquaculture Research 31, 11–23.CrossRefGoogle Scholar
Kwiecinska, P, Rosziewicz, B, ̡okociejewska, M, Orzechowski, A 2005. Elevated expression of NF-κB and Bcl-2 proteins in C2C12 myocytes during myogenesis is affected by PD98059, LY294002 or SB203580 treatments. Cell Biology International 29, 319–331.CrossRefGoogle ScholarPubMed
Larzul, C, Gondret, F, Combes, S, de Rochambeau, H 2005. Divergent selection on 63-day body weight in the rabbit: response on growth, carcass and muscle traits. Genetics Selection Evolution 37, 105–122.CrossRefGoogle ScholarPubMed
Le Bihan-Duval, E, Beaumont, C, Colleau, JJ 1996. Genetic parameters of the twisted legs syndrome in broiler chickens. Genetics Selection Evolution 28, 177–195.CrossRefGoogle Scholar
Le Bihan-Duval, E, Berri, C, Pitel, F, Nadaf, J, Sibut, V, Jenkins, C, Duclos, MJ 2007. A general approach combining QTL research and gene expression profiling to identify genes controlling chicken meat quality. Sciences des Aliments 27, 143–152.CrossRefGoogle Scholar
Le Bihan-Duval, E, Debut, M, Berri, CM, Sellier, N, Sante-Lhoutellier, V, Jego, Y, Beaumont, C 2008. Chicken meat quality: genetic variability and relationship with growth and muscle characteristics. BMC Genetics 9, 6.CrossRefGoogle ScholarPubMed
Lefaucheur, L 2006. Myofibre typing and its relationships to growth performance and meat quality. Archives of Animal Breeding 49 (Special Issue), 4–17.Google Scholar
Lefaucheur, L, Ecolan, P 2005. Pattern of muscle fiber formation in Large White and Meishan pigs. Archives of Animal Breeding 48 (Special Issue), 117–122.Google Scholar
Lefaucheur, L, Ecolan, P 2007. Changes in muscle proteome during development in the pig. Archives of Animal Breeding 50 (Special Issue), 15–16.Google Scholar
Lefaucheur, L, Milan, D, Ecolan, P, Le Callennec, C 2004. Myosin heavy chain composition of different skeletal muscles in Large White and Meishan pigs. Journal of Animal Science 82, 1931–1941.CrossRefGoogle ScholarPubMed
Lefaucheur, L, Ecolan, P, Lebret, B, Damon, M, Louveau, I, Sellier, P, Gilbert, H 2005. Influence of divergent selection on residual feed intake in the growing pig on muscle compositional traits. Archives of Animal Breeding 51 (Special Issue 1), 117–122.Google Scholar
Lefaucheur, L, Lebret, B, Ecolan, P, Galian, M, Damon, M, Louveau, I, Prunier, A, Sellier, P, Gilbert, H 2008. Sélection divergente pour la consommation alimentaire résiduelle chez le porc: effets sur les propriétés musculaires et la qualité de la viande. Journées de la Recherche Porcine en France 40, 83–84.Google Scholar
Liu, ZJ, Cordes, JF 2004. DNA marker technologies and their applications in aquaculture genetics. Aquaculture 238, 1–37.CrossRefGoogle Scholar
Liu, J, Damon, M, Guitton, N, Guisle, I, Ecolan, P, Vincent, A, Cherel, P, Gondret, F 2009. Differentially-expressed genes in pig longissimus muscles with contrasting levels of fat, as identified by combined transcriptomic, reverse transcription PCR, and proteomic analyses. Journal of Agricultural and Food Chemistry 57, 3808–3817.CrossRefGoogle ScholarPubMed
Liu, G, Jennen, DG, Tholen, E, Juengst, H, Kleinwachter, T, Holker, M, Tesfaye, D, Un, G, Schreinemachers, HJ, Muráni, E, Ponsuksili, S, Kim, JJ, Schellander, K, Wimmers, K 2007. A genome scan reveals QTL for growth, fatness, leanness and meat quality in a Duroc–Piétrain resource population. Animal Genetics 38, 241–252.CrossRefGoogle Scholar
Maak, S, Neumann, K, Swalve, HH 2006. Identification and analysis of putative regulatory sequences for the MYF5/MYF6 locus in different vertebrate species. Gene 379, 141–147.CrossRefGoogle ScholarPubMed
Mau, M, Kalbe, C, Viergutz, T, Nürnberg, G, Rehfeldt, C 2008a. Effects of dietary isoflavones on proliferation and DNA integrity of myoblasts derived from newborn piglets. Pediatric Research 63, 39–45.CrossRefGoogle ScholarPubMed
Mau, M, Kalbe, C, Wollenhaupt, K, Nürnberg, G, Rehfeldt, C 2008b. IGF-I- and EGF dependent porcine myoblast proliferation is influenced by the dietary isoflavones genistein and daidzein. Domestic Animal Endocrinology 35, 281–289.CrossRefGoogle Scholar
Moghadam, HK, Poissant, J, Fotherby, H, Haidle, L, Ferguson, MM, Danzmann, RG 2007. Quantitative trait loci for body weight, condition factor and age at sexual maturation in Arctic charr (Salvelinus alpinus): comparative analysis with rainbow trout (Oncorhynchus mykiss) and Atlantic salmon (Salmo salar). Molecular Genetics and Genomics 277, 647–661.CrossRefGoogle ScholarPubMed
Montserrat, N, Sánchez-Gurmaches, J, García de la Serrana, D, Navarro, M, Gutiérrez, J 2007. IGF-I binding and receptor signal transduction in primary cell culture of muscle cells of gilthead sea bream: changes throughout in vitro development. Cell and Tissue Research 330, 503–513.CrossRefGoogle ScholarPubMed
Muráni, E, Ponsuksili, S, Wimmers, K 2007a. Investigation of genetic and epigenetic mechanisms underlying stage- and breed-specific differences in the transcription of S 1gene during porcine myogenesis. Archives of Animal Breeding 50 (Special Issue), 49–56.Google Scholar
Muráni, E, Muraniova, M, Ponsuksili, S, Schellander, K, Wimmers, K 2007b. Identification of genes differentially expressed during prenatal development of skeletal muscle in two pig breeds differing in muscularity. BMC Developmental Biology 7, 109.CrossRefGoogle ScholarPubMed
Muráni, E, Westphal, P, Ponsuksili, S, Wimmers, K 2008. Investigation of the porcine SMAD7 gene as a functional-positional candidate for muscle-related traits. Archives of Animal Breeding 51 (Special Issue 1), 71.Google Scholar
Nadaf, J, Gilbert, H, Pitel, F, Berri, CM, Féve, K, Beaumont, C, Duclos, MJ, Vignal, A, Porter, TE, Simon, J, Aggrey, SE, Cogburn, LA, Le Bihan-Duval, E 2007. Identification of QTL controlling meat quality traits in an F2 cross between two chicken lines selected for either low or high growth rate. BMC Genomics 8, 155.CrossRefGoogle ScholarPubMed
Nissen, PM, Oksbjerg, N 2009. In vitro primary satellite cell growth and differentiation within litters of pigs. Animal 5, 703–709.CrossRefGoogle Scholar
Nissen, PM, Sørensen, IL, Vestergaard, M, Oksbjerg, N 2005. Effects of sow nutrition on maternal and foetal serum growth factors and on foetal myogenesis. Animal Science 80, 299–306.CrossRefGoogle Scholar
Oliván, M, Martínez, A, Osoro, K, Sañudo, C, Panea, B, Olleta, JL, Campo, MM, Oliver, MA, Serra, X, Gil, M, Piedrafita, J 2004. Effect of muscular hypertrophy on physico-chemical, biochemical and texture traits of meat from yearling bulls. Meat Science 68, 567–575.CrossRefGoogle ScholarPubMed
Orzechowski, A, ̡okociejewska, M, Pawlikowska, P, Kruszewski, M 2005. Preincubation with sodium ascorbate potentiates insulin-dependent PKB/Akt and c-Jun phosphorylation in L6 rat myoblasts challenged with reactive oxygen/nitrogen species. Life Sciences 77, 496–511.CrossRefGoogle ScholarPubMed
Pawlikowska, P, Gajakowska, B, Orzechowski, A 2007a. Mitofusin (Mfn2) – a key player in insulin-dependent myogenesis in vitro. Cell and Tissue Research 327, 571–581.CrossRefGoogle ScholarPubMed
Pawlikowska, P, ̡okociejewska, M, Hocquette, JF, Orzechowski, A 2007b. Changes in the expression of proteins involved in insulin signalling and metabolic properties of energy supply elucidate skeletal muscle-type specific resistance to glucocorticoid-induced muscle cachexia. In Energy and protein metabolism and nutrition (ed. I Ortigues-Marty, N Miraux and W Brand-Williams), pp. 177–179. EAAP publication No. 124, Wageningen Academic Publishers, The Netherlands.CrossRefGoogle Scholar
Peter, JB, Barnard, RJ, Edgerton, VR, Gillespie, CA, Stempel, KE 1972. Metabolic profiles of three fiber types of skeletal muscle in guinea pigs and rabbits. Biochemistry 11, 2627–2633.CrossRefGoogle Scholar
Picard, B, Jurie, C, Duris, MP, Renand, G 2005. Consequences of selection for higher growth rate on muscle fibre properties in cattle. Livestock Production Sciences 102, 107–120.Google Scholar
Picard, B, Lefaucheur, L, Berri, C, Duclos, MJ 2002. Muscle fibre ontogenesis in farm animal species. Reproduction Nutrition and Development 42, 415–431.CrossRefGoogle ScholarPubMed
Ponsuksili, S, Nguyen Trong, Ngu, Muráni, E, Schellander, K, Wimmers, K 2008. Relative abundance of MyHC isoform transcripts and its association with muscularity and meat quality. Archives of Animal Breeding 51 (Special Issue 1), 40.Google Scholar
Puolanne, E, Räsänen, P 2008. A method for determining the muscle fibre length. Archives of Animal Breeding 51 (Special Issue 1), 41–44.Google Scholar
Räsänen, P, Puolanne, E 2004. A method for determining the muscle fibre length. Proceedings o the 50th International Congress of Meat Science and Technology. August 8–13, 2004 – Helsinki, Finland, pp. 258–260.CrossRefGoogle Scholar
Ramirez, JA, Oliver, MA, Pla, M, Guerrero, L, Ariño, B, Blasco, A, Pascual, M, Gil, M 2004. Effect of selection for growth rate on biochemical, quality and texture characteristics of meat from rabbits. Meat Science 67, 617–624.CrossRefGoogle ScholarPubMed
Rehfeldt, C, Fiedler, I, Stickland, NC 2004a. Number and size of muscle fibres in relation to meat production. In Muscle development of livestock animals – physiology, genetics, and meat quality(ed. MFW Te Pas, ME Everts and HP Haagsman), pp. 1–38. CABI Publishing, Wallingford, UK.Google Scholar
Rehfeldt, C, Renne, U, Wittstock, M, Mix, E, Zettl, UK 2004b. Long-term growth selection of mice changes the intrinsic susceptibility of myogenic cells to apoptosis. Journal of Muscle Research and Cell Motility 25, 177–185.CrossRefGoogle ScholarPubMed
Rehfeldt, C, Henning, M, Fiedler, I 2008. Consequences of pig domestication for skeletal muscle growth and cellularity. Livestock Science 116, 30–41.CrossRefGoogle Scholar
Rehfeldt, C, Ott, G, Gerrard, DE, Varga, L, Schlote, W, Williams, JL, Renne, U, Bünger, L 2005. Effects of the Compact mutant myostatin allele Mstn (Cmpt-dl1Abc) introgressed into a high growth mouse line on skeletal muscle cellularity. Journal of Muscle Research and Cell Motility 26, 103–112.CrossRefGoogle ScholarPubMed
Rehfeldt, C, Te Pas, MFW, Wimmers, K, Brameld, JM, Nissen, PM, Berri, C, Valente, LMP, Power, D, Picard, B, Stickland, NC, Oksbjerg, N 2011. Advances in research on the prenatal development of skeletal muscle in animals in relation to the quality of muscle-based food. I. Regulation of myogenesis and environmental impact. Animal, doi:10.1017/S1751731110002089.Google Scholar
Reid, DP, Szanto, A, Glebe, B, Danzmann, RG, Ferguson, MM 2005. QTL for body weight and condition factor in Atlantic salmon (Salmo salar): comparative analysis with rainbow trout (Oncorhynchus mykiss) and Arctic charr (Salvelinus alpinus). Heredity 94, 166–172.CrossRefGoogle ScholarPubMed
Rescan, P-Y, Montfort, J, Rallière, C, Le Cam, A, Esquerré, D, Hugot, K 2007. Dynamic gene expression in fish muscle during recovery growth induced by a fasting–refeeding schedule. BMC Genomics 8, 438.CrossRefGoogle ScholarPubMed
Ruusunen, M, Puolanne, E 2004. Histochemical properties of fibre types in muscles of wild and domestic pigs and the effect of growth rate on muscle fibre properties. Meat Science 67, 533–539.CrossRefGoogle ScholarPubMed
Scanes, CG, Dunnington, EA, Buonomo, FC, Donoghue, DJ, Siegel, PB 1989. Plasma concentrations of insulin like growth factors (IGF-)I and IGF-II in dwarf and normal chickens of high and low weight selected lines. Growth Development and Aging 53, 151–157.Google ScholarPubMed
Seo, K, Beever, JE 2001. Monitoring gene expression in swine skeletal muscle. Abstracts of the Plant and Animal Genomes IX Conference, San Diego, CA, USA, 207pp.Google Scholar
Sibut, V, Le Bihan-Duval, E, Tesseraud, S, Godet, E, Bordeau, T, Cailleau-Audouin, E, Chartrin, P, Duclos, MJ, Berri, C 2008. Adenosine monophosphate-activated protein kinase involved in variations of muscle glycogen and breast meat quality between lean and fat chickens. Journal of Animal Science 86, 2888–2896.CrossRefGoogle ScholarPubMed
Sirin, E, Sayli, O, Ulutas, Z, Sen, U, Erdogan, SB, Aksoy, Y, Akin, A, Kuran, M 2008. Can functional near infrared spectroscopy (fNIRS) be used for the estimation of the numbers and types of muscle fibres in sheep? Archives of Animal Breeding 51 (Special Issue 1), 45–46.Google Scholar
Stickland, NC, Bayol, S, Ashton, C, Rehfeldt, C 2004. Manipulation of muscle fibre number during prenatal development. In:Muscle development of livestock animals – physiology, genetics, and meat quality (ed. MFW Te Pas, ME Everts and HP Haagsman), pp. 69–82. CABI Publishing, Wallingford, UK.CrossRefGoogle Scholar
Stinckens, A, Van den Maagdenberg, K, Luyten, L, Georges, M, De Smet, S, Buys, N 2007. The RYR1g.1843C>T mutation is associated with the effect of the IGF2 intron-3-g3072G>A mutation on muscle hypertrophy. Animal Genetics 38, 67–71.CrossRefGoogle ScholarPubMed
Te Pas, MFW, Soumillion, A 2001. The use of physiologic and functional genomic information of the regulation of the determination of skeletal muscle mass in livestock breeding strategies to enhance meat production. Current Genomics 2, 285–304.CrossRefGoogle Scholar
Te Pas, MFW, Hulsegge, I, Pool, MH 2007a. Pathway analysis: combining microarray data and physiological data to study myogenesis. Archives of Animal Breeding 50 (Special Issue), 27–31.Google Scholar
Te Pas, MFW, Hulsegge, I, Pool, MH, Coster, A, Heuven, HH, Janss, LLG 2007b. Biochemical pathways analysis of microarray results: regulation of myogenesis. BMC Developmental Biology 7, 66.CrossRefGoogle ScholarPubMed
Te Pas, MFW, Verburg, FJ, Gerritsen, CLM, de Greef, KH 2000. Messenger ribonucleic acid expression of the MyoD gene family in muscle tissue at slaughter in relation to selection for porcine growth rate. Journal of Animal Science 78, 69–77.CrossRefGoogle ScholarPubMed
Te Pas, MFW, Pool, MH, Hulsegge, I, Janss, LLG 2006. Analysis of the differential transcriptome expression profiles during prenatal muscle tissue development. Archives of Animal Breeding 49 (Special Issue), 110–115.Google Scholar
Te Pas, MFW, Jansen, J, Broekman, KCJA, Reimert, H, Heuven, HCM 2008. Post mortem proteome degradation profiles of longissimus muscle in Yorkshire and Duroc. Archives of Animal Breeding 51 (Special Issue 1), 62.Google Scholar
Te Pas, MFW, Harders, FL, Soumillion, A, Born, L, Buist, W, Meuwissen, THE 1999a. Genetic variation at the porcine myf-5 gene locus – lack of association with meat production traits. Mammalian Genome 10, 123–127.CrossRefGoogle ScholarPubMed
Te Pas, MFW, Soumillion, A, Harders, FL, Verburg, FJ, van den Bosch, TJ, Galesloot, P, Meuwissen, THE 1999b. Influences of myogenin genotype on birth weight, growth rate, carcass weight, backfat thickness and lean weight of pigs. Journal of Animal Science 77, 2352–2356.CrossRefGoogle ScholarPubMed
Te Pas, MFW, Cagnazzo, M, de Wit, AAC, Priem, J, Pool, M, Davoli, R 2005a. Muscle transcriptomes of Duroc and Piétrain pig breeds during prenatal formation of skeletal muscle tissue using microarray technology. Archives of Animal Breeding 48 (Special Issue), 141–147.Google Scholar
Te Pas, MFW, de Wit, A, Priem, J, Cagnazzo, M, Davoli, R, Russo, V, Pool, MH 2005b. Transcriptome expression profiles in prenatal pigs in relation to myogenesis. Journal of Muscle Research and Cell Motility 26, 157–165.CrossRefGoogle ScholarPubMed
Tesseraud, S, Pym, RAE, Le Bihan-Duval, E, Duclos, MJ 2003. Response of broilers selected on carcass quality to dietary protein supply: live performance, muscle development and circulating insulin-like growth factors (IGF-I and -II). Poultry Science 82, 1011–1016.CrossRefGoogle ScholarPubMed
Theil, PK, Sørensen, IL, Nissen, PM, Oksbjerg, N 2006. Temporal gene expression of growth factors of primary porcine satellite cells during myogenesis in response to exogenous insulin. Animal Science Journal 77, 330–337.CrossRefGoogle Scholar
Tygesen, MP, Harrison, AP 2005. Nutritional restriction in utero programs postnatal muscle development in lambs. Animal Science Journal 76, 261–271.CrossRefGoogle Scholar
Tygesen, MP, Harrison, AP, Therkildsen, M 2007. The effect of maternal nutrient restriction during late gestation on muscle fibre size, bone and slaughter parameters in five month old lambs. Livestock Production Science 110, 230–241.CrossRefGoogle Scholar
Valente, LMP, Moreira, S, Ralliere, C, Ramos, AM, Rescan, PY 2006. Variability of myostatin genes in rainbow trout (Oncorhynchus mykiss) strains exhibiting distinct hyperplastic growth: preliminary results. Archives of Animal Breeding 49 (Special Issue), 103–108.Google Scholar
Van den Maagdenberg, K, Claeys, E, Stinckens, A, Buys, N, De Smet, S 2007a. Effect of age, muscle type, and insulin-like growth factor-II genotype on muscle proteolytic and lipolytic enzyme activities in boars. Journal of Animal Science 85, 952–960.CrossRefGoogle ScholarPubMed
Van den Maagdenberg, K, Stinckens, A, Lefaucheur, L, Buys, N, De Smet, S 2007b. The effect of mutations in the insulin-like growth factor-II and ryanodine receptor-1 genes on biochemical and histochemical muscle fibre characteristics in pigs. Meat Science 79, 757–799.CrossRefGoogle ScholarPubMed
Van den Maagdenberg, K, Stinckens, A, Claeys, E, Buys, N, De Smet, S 2008. Effect of the insulin-like growth factor-II and RYR1 genotype in pigs on carcass and meat quality traits. Meat Science 80, 293–303.CrossRefGoogle ScholarPubMed
Van de Wiel, DFM, Zhang, WL 2007. Identification of pork quality parameters by proteomics. Meat Science 77, 46–54.CrossRefGoogle ScholarPubMed
Wimmers, K, Muráni, E, Schellander, K, Ponsuksili, S 2005. Combining QTL- and expression-analysis: identification of functional positional candidate genes for meat quality and carcass traits. Archives of Animal Breeding 48 (Special Issue), 23–31.Google Scholar
Wimmers, K, Ngu, NT, Muráni, E, Schellander, K, Ponsuksili, S 2006a. Linkage and expression analysis to elucidate the genetic background of muscle structure and meat quality in the pig. Archives of Animal Breeding 49 (Special Issue), 116–125.Google Scholar
Wimmers, K, Fiedler, I, Hardge, T, Muráni, E, Schellander, K, Ponsuksili, S 2006b. QTL for microstructural and biophysical muscle properties and body composition in pigs. BMC Genetics 7, 15.CrossRefGoogle ScholarPubMed
Wimmers, K, Ngu, NT, Jennen, DG, Tesfaye, D, Muráni, E, Schellander, K, Ponsuksili, S 2008. Relationship between myosin heavy chain isoform expression and muscling in several diverse pig breeds. Journal of Animal Science 86, 795–803.CrossRefGoogle ScholarPubMed
Wimmers, K, Muráni, E, Te Pas, MFW, Chang, KC, Davoli, R, Merks, JWM, Henne, H, Muraniova, M, da Costa, N, Harlizius, B, Schellander, K, Böll, I, Braglia, S, de Wit, AAC, Cagnazzo, M, Fontanesi, L, Prins, D, Ponsuksili, S 2007. Associations of functional candidate genes derived from gene expression profiles of prenatal porcine muscle tissue with meat quality and muscle deposition. Animal Genetics 38, 474–484.CrossRefGoogle ScholarPubMed
Wu, G, Bazer, FW, Datta, S, Gao, H, Johnson, GA, Lassala, A, Li, P, Satterfield, MC, Spencer, TE 2008. Intrauterine growth retardation in livestock: implications, mechanisms and solutions. Archives of Animal Breeding 51 (Special Issue 1), 4–10.Google Scholar
Zhao, SH, Nettleton, D, Liu, W, Fitzsimmons, C, Ernst, CW, Raney, NE, Tuggle, CK 2003. Complementary DNA macroarray analyses of differential gene expression in porcine fetal and postnatal muscle. Journal of Animal Science 81, 2179–2188.CrossRefGoogle ScholarPubMed