Mutations with known links to pork quality defects in Norwegian and German pig populations

References

• Barbut, S., Sosnicki, A. A., Lonergan, S. M., Knapp, T., Ciobanu, D. C., Gatcliffe, L. J., Huff-Lonergan, E. & Wilson, E. W. (2008). Progress in reducing the pale, soft and exudative (PSE) problem in pork and poultry meat. Meat Science, 79(1), 46–63. doi:10.1016/j.meatsci.2007.07.031
   PubMed Web of Science ®Google Scholar
• Brewer, M. S. & McKeith, F. K. (1999). Consumer-rated quality characteristics as related to purchase intent of fresh pork. Sensory Evaluation, 64(1), 171–174.
   Google Scholar
• Ciobanu, D., Bastiaansen, J., Malek, M., Helm, J., Woollard, J., Plastow, G. & Rothschild, M. (2001). Evidence for new alleles in the protein kinase adenosine monophosphate-activated 3-subunit gene associated with low glycogen content in pig skeletal muscle and improved meat quality. https://academic.oup.com/genetics/article/159/3/1151/6049531.
   Google Scholar
• Josell, Å, Gv, S. & Tornberg, E. (2003). Sensory quality and the incidence of PSE of pork in relation to crossbreed and RN phenotype. Meat Science, 65(1), 651–660. doi:10.1016/S0309-1740(02)00268-1
   PubMed Web of Science ®Google Scholar
• Ma, J., Yang, J., Zhou, L., Ren, J., Liu, X., Zhang, H., Yang, B., Zhang, Z., Ma, H., Xie, X., et al. (2014). A splice mutation in the PHKG1 gene causes high glycogen content and low meat quality in pig skeletal muscle. PLoS Genetics, 10(10), e1004710. doi:10.1371/journal.pgen.1004710
   PubMed Web of Science ®Google Scholar
• Mashood, Q., Karlsson, A. H., Wallenbeck, A., Eriksson, S., Johansson, A. M. & Segerkvist, K. A. (2023). A review on pale, soft, and exudative (PSE)-like zones in pork: current knowledge on underlying factors and identification of knowledge gaps for further research. Acta Agriculturae Scandinavica A: Animal Sciences.
   Web of Science ®Google Scholar
• Mérour, I., Hermesch, S., Schwob, S. & Tribout, T. (2009). Effect of the halothane genotype on growth performances, carcass and meat quality traits in the Pietrain breed of the French national pig breeding program. Proc. Assoc. Advmt. Anim. Breed. Genet, 18, 191–194.
   Google Scholar
• Mickelson, J. R., Gallant, E. M., Litterer, L. A., Johnson, K. M., Rempel, W. E. & Louis, C. F. (1988). Abnormal sarcoplasmic reticulum ryanodine receptor in malignant hyperthermia. Journal of Biological Chemistry, 263(19), 9310–9315. doi:10.1016/s0021-9258(19)76541-7
   PubMed Web of Science ®Google Scholar
• Mickelson, J. R., Gallant, E. M., Rempel, W. E., Johnson, K. M., Litterer, L. A., Jacobson, B. A. & Louis, C. F. (1989). Effects of the halothane-sensitivity gene on sarcoplasmic reticulum function. American Journal of Physiology-Cell Physiology, 257(4), C787–C794. doi:10.1152/ajpcell.1989.257.4.C787
   Google Scholar
• Milan, D., Jeon, J. T., Looft, C., Amarger, V., Robic, A., Thelander, M., Rogel-Gaillard, C., Paul, S., Iannuccelli, N., Rask, L., et al. (2000). A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle. Science, 288(5469), 1248–1251. http://www.ncbi.nlm.nih.gov/pubmed/10818001.
   PubMed Web of Science ®Google Scholar
• Muñoz, M., Bozzi, R., García, F., Núñez, Y., Geraci, C., Crovetti, A., García-Casco, J., Alves, E., Škrlep, M., Charneca, R., et al. (2018). Diversity across major and candidate genes in European local pig breeds. PLoS One, 13(11), e0207475. doi:10.1371/journal.pone.0207475
   PubMed Web of Science ®Google Scholar
• Nakajima, E., Matsumoto, T., Yamada, R., Kawakami, K., Takeda, K., Ohnishi, A. & Komatsu, M. (1996). Technical note: use of a PCR-single strand conformation polymorphism (PCR-SSCP) for detection of a point mutation in the swine ryanodine receptor (RYR1) gene. Journal of Animal Science, 74(12), 2904. doi:10.2527/1996.74122904x
   PubMed Web of Science ®Google Scholar
• Ollivier, L., Sellier, P. & Monin, G. (1975). Déterminisme génétique du syndrome d'hyperthermie maligne chez le porc de Pietrain. Ann. Génét Sél Anim, 7, 159–166. doi:10.1186/1297-9686-7-2-159
   PubMedGoogle Scholar
• Scheffler, T. L. & Gerard, D. E. (2007). Mechanisms controlling pork quality development: The biochemistry controlling postmortem energy metabolism. Meat Science, 77(1), 7–16. doi:10.1016/J.MEATSCI.2007.04.024
   PubMed Web of Science ®Google Scholar
• Scheffler, T. L. & Gerard, D. E. (2016). Growth and development symposium: adenosine monophosphate–activated protein kinase and mitochondria in rendement napole pig growth. Journal of Animal Science, 94(9), 3601–3612. doi:10.2527/jas.2015-0055
   PubMed Web of Science ®Google Scholar
• Skrlep, M. & Sante-Lhoutellier, V. (2009). Effect of I199 V polymorphism on prkag3 gene on carcass and meat quality traits in slovenian commercial pigs. Journal of Muscle Foods [Internet], 20(3), 367–376.
   Google Scholar
• Sudhakar, A., Khade, A., Nayee, N., Reddy, R. V. C. & Maurya, B. (2021). Novel mutation in UMPS gene leads to false positive result of DUMPS (genetic disorder) in buffaloes: need for gene sequencing before confirming results of RFLP in new species. Journal of Genetics, 100(2), 55. doi:10.1007/s12041-021-01305-2
   PubMed Web of Science ®Google Scholar
• Suliga, P., Abie, S. M., Egelandsdal, B., Alvseike, O., Johny, A., Kathiresan, P. & Münch, D. (2022). Beyond standard PSE testing: An exploratory study of bioimpedance as a marker for ham defects. Meat Science, 194, 108980. doi:10.1016/j.meatsci.2022.108980
   PubMed Web of Science ®Google Scholar
• Vinje, H., Brustad, H. K., Heggli, A., Sevillano, C. A., Van Son, M. & Gangsei, L. E. (2023). Classification of breed combinations for slaughter pigs based on genotypes—modeling DNA samples of crossbreeds as fuzzy sets from purebred founders. Frontiers in Genetics, 14, e1289130. doi:10.3389/fgene.2023.1289130
   PubMed Web of Science ®Google Scholar