Potential Functional Variants for Fatness, Carcass and Meat Quality Traits in Exon 3 of Fat Mass and Obesity-Associated Gene in Indonesian Ducks
DOI:
https://doi.org/10.3923/ijps.2018.443.451Keywords:
Carcass, ducks, fat mass and obesity-associated gene, fatty acids, mRNA expressionAbstract
Background and Objective: The fat mass and obesity-associated gene (FTO) regulates glucose metabolism, body weight and fat content, it is also involved in DNA repair, fatty acid (FA) metabolism and post translational modification. Due to these functions, FTO may affect FAs, carcass and meat quality in ducks. The objective of this study was to identify functional variants of FTO associated with fatness, carcass and meat quality and to investigate the tissue expression profile of the FTO gene in ducks. Methodology: Fifty-seven Indonesian Cihateup ducks were used in this study. Tissues from breast muscle and liver were used to evaluate genomic DNA and mRNA expression. Fatness traits, which include FA composition, carcass and meat quality, were evaluated at 12 weeks. Results: A SNP in exon 3 of the SCD gene was significantly associated with breast muscle for carcass traits and lauric acid (C12:0) for FA composition, however, there was no significant association with meat quality traits. To measure the mRNA expression of FTO, ducks were divide into three genotypes (AA, AG and GG). Compared to the AG and GG genotype, the AA genotype ducks had greater breast muscle weight and higher lauric acid levels (C12:0) for carcass and FA traits, respectively. FTO mRNA expression was significantly higher in genotype AA and GG ducks. Conclusion: The SNP of FTO in exon 3 is a functional SNP that regulates carcass and FAs specific for breast muscle weight and lauric acid levels in ducks.
References
Cheung, M.K.M. and G. Yeo, 2011. FTO biology and obesity: Why do a billion of us weigh 3 kg more? Front. Endocrinol., Vol. 2.
Simopoulos, A., 2016. The FTO gene, browning of adipose tissue and omega-3 fatty acids. Lifestyle Genomics, 9: 123-126.
Locke, A.E., B. Kahali, S.I. Berndt, A.E. Justice and T.H. Pers et al., 2015. Genetic studies of body mass index yield new insights for obesity biology. Nat., 518: 197-206.
Sun, F., R. Tu, J.H. Xia, X.J. Liu and G.H. Yue, 2018. The FTO gene is associated with growth and omega-3/-6 ratio in Asian Seabass. Mar. Biotechnol.
Fredriksson, R., M. Hagglund, P.K. Olszewski, O. Stephansson and J.A. Jacobsson et al., 2008. The obesity gene, FTO, is of ancient origin, up-regulated during food deprivation and expressed in neurons of feeding-related nuclei of the brain. Endocrinology, 149: 2062-2071.
Binh, T.Q., P.T. Phuong, B.T. Nhung, D.D. Thoang, H.T. Lien and D. Van Thanh, 2013. Association of the common FTO-rs9939609 polymorphism with type 2 diabetes, independent of obesity-related traits in a Vietnamese population. Gene, 513: 31-35.
Hubacek, J.A., V. Staněk, M. Gebauerova, A. Pilipcincova and D. Dlouha et al., 2010. A FTO variant and risk of acute coronary syndrome. Clin. Chim. Acta, 411: 1069-1072.
Church, C., L. Moir, F. McMurray, C. Girard and G.T. Banks et al., 2010. Overexpression of Fto leads to increased food intake and results in obesity. Nature Genet., 42: 1086-1092.
Jiao, Y., J. Zhang, L. Lu, J. Xu and L. Qin, 2016. The Fto gene regulates the proliferation and differentiation of pre-adipocytes in vitro. Nutrients, Vol. 8.
Wang, C.Y., S.S. Shie, M.S. Wen, K.C. Hung, I.C. Hsieh, T.S. Yeh and D. Wu, 2015. Loss of FTO in adipose tissue decreases Angptl4 translation and alters triglyceride metabolism. Sci. Signal., 8: ra127-ra127.
Bravard, A., E. Lefai, E. Meugnier, S. Pesenti and E. Disse et al., 2011. FTO is increased in muscle during type 2 diabetes and its overexpression in myotubes alters insulin signaling, enhances lipogenesis and ROS production and induces mitochondrial dysfunction. Diabetes, 60: 258-268.
Zhang, J., S. Li, J. Li, C. Han and Z. Wang et al., 2014. Expression and significance of fat mass and obesity associated gene and forkhead transcription factor O1 in non-alcoholic fatty liver disease. Chinese Med. J., 127: 3771-3776.
Ikels, K., S. Kuschel, J. Fischer, W. Kaisers, D. Eberhard and U. Ruther, 2014. FTO is a relevant factor for the development of the metabolic syndrome in mice. Plos One, Vol. 9.
Wei, S., L. Zan, J.A. Ujan, H. Wang, Y. Yang and C. Adoligbe, 2011. Novel polymorphism of the bovine fat mass and obesity-associated (FTO) gene are related to backfat thickness and longissimus muscle area in five Chinese native cattle breeds. Afr. J. Biotechnol., 10: 2820-2824.
Fontanesi, L., E. Scotti, L. Buttazzoni, S. Dall'Olio and A. Bagnato et al., 2010. Confirmed association between a single nucleotide polymorphism in the FTO gene and obesity-related traits in heavy pigs. Mol. Biol. Rep., 37: 461-466.
Szydlowski, M., S. Salamon, M. Grzes and M. Switonski, 2012. SNP in the 5' flanking region of the pig FTO gene is associated with fatness in Polish Landrace. Livestock Sci., 150: 397-400.
Yu, K., G. Shu, F. Yuan, X. Zhu and P. Gao et al., 2013. Fatty acid and transcriptome profiling of longissimus dorsi muscles between pig breeds differing in meat quality. Int. J. Biol. Sci., 9: 108-118.
Cameron, N.D., M. Enser, G.R. Nute, F.M. Whittington and J.C. Penman et al., 2000. Genotype with nutrition interaction on fatty acid composition of intramuscular fat and the relationship with flavour of pig meat. Meat Sci., 55: 187-195.
Woollett, L.A., D.K. Spady and J.M. Dietschy, 1992. Saturated and unsaturated fatty acids independently regulate low density lipoprotein receptor activity and production rate. J. Lipid Res., 33: 77-88.
Pascual, J.V., M. Rafecas, M.A. Canela, J. Boatella, R. Bou, A.C. Barroeta and R. Codony, 2007. Effect of increasing amounts of a linoleic-rich dietary fat on the fat composition of four pig breeds. Part II: Fatty acid composition in muscle and fat tissues. Food Chem., 100: 1639-1648.
Geng, X., S. Liu, Z. Yuan, Y. Jiang, D. Zhi and Z. Liu, 2017. A genome-wide association study reveals that genes with functions for bone development are associated with body conformation in catfish. Mar. Biotechnol., 19: 570-578.
Zhao, L., Y. Li, Y. Li, J. Yu and H. Liao et al., 2017. A genome-wide association study identifies the genomic region associated with shell color in yesso scallop, Patinopecten yessoensis. Mar. Biotechnol., 19: 301-309.
Tamzil, M.H. and B. Indarsih, 2017. Measurement of phenotype characteristics of sasak ducks: Indian Runner ducks of Lombok Island Indonesia. Anim. Prod., 19: 13-19.
Muzani, A., B. Brahmantiyo, C. Sumantri and A. Tapyadi, 2005. Pendugaan jarak genetik pada itik Cihateup, Cirebon, dan Mojosari. Med. Pet., 28: 109-116.
Matitaputty, P.R., R.R. Noor, P.S. Hardjosworo and C.H. Wijaya, 2011. Performa, persentase karkas dan nilai heterosis itik Alabio, Cihateup dan hasil persilangannya pada umur delapan minggu. JITV., 16: 90-97.
Anggraeni, A. Gunawan, Rukmiasih, T. Suryati and C. Sumantri, 2017. Association and expression analyses of the duck FMO3 gene in relation to fatty acid composition. Int. J. Poult. Sci., 16: 486-493.
Lee, E.A., J.M. Kim, K.S. Lim, Y.C. Ryu, W.M. Jeon and K.C. Hong, 2012. Effects of variation in porcine MYOD1 gene on muscle fiber characteristics, lean meat production and meat quality traits. Meat Sci., 92: 36-43.
Folch, J., M. Lees and G.H.S. Stanley, 1957. A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem., 226: 497-509.
Gan, W., Q. Song, N.N. Zhang, X.P. Xiong, D.M.C. Wang and L. Li, 2015. Association between FTO polymorphism in exon 3 with carcass and meat quality traits in crossbred ducks. Genet. Mol. Res., 14: 6699-6714.
Rozen, S. and H. Skaletsky, 2000. Primer3 on the WWW for general users and for biologist programmers. Methods Mol. Biol., 132: 365-386.
Gunawan, A., S. Sahadevan, C. Neuhoff, C. Große-Brinkhaus and A. Gad et al., 2013. RNA deep sequencing reveals novel candidate genes and polymorphisms in boar testis and liver tissues with divergent androstenone levels. Plos One, Vol. 8.
Gunawan, A., S. Sahadevan, M.U. Cinar, C. Neuhoff and C. Große-Brinkhaus et al., 2013. Identification of the novel candidate genes and variants in boar liver tissues with divergent skatole levels using RNA deep sequencing. PloS One, Vol. 8.
Cinar, M.U., A. Kayan, M.J. Uddin, E. Jonas and D. Tesfaye et al., 2012. Association and expression quantitative trait loci (eQTL) analysis of porcine AMBP, GC and PPP1R3B genes with meat quality traits. Mol. Biol. Rep., 39: 4809-4821.
Kayan, A., M.U. Cinar, M.J. Uddin, C. Phatsara and K. Wimmers et al., 2011. Polymorphism and expression of the porcine Tenascin C gene associated with meat and carcass quality. Meat Sci., 89: 76-83.
Silver, N., S. Best, J. Jiang and S.L. Thein, 2006. Selection of housekeeping genes for gene expression studies in human reticulocytes using real-time PCR. BMC Mol. Biol. Vol. 7.
Rempel, L.A., E. Casas, S.D. Shackelford and T.L. Wheeler, 2012. Relationship of polymorphisms within metabolic genes and carcass traits in crossbred beef cattle. J. Anim. Sci., 90: 1311-1316.
Fontanesi, L., E. Scotti, L. Buttazzoni, R. Davoli and V. Russo, 2009. The porcine fat mass and obesity associated (FTO) gene is associated with fat deposition in Italian Duroc pigs. Anim. Genet., 40: 90-93.
Fu, Y., L. Li and S. Ren, 2013. Effect of FTO expression and polymorphism on fat deposition in Suzhong pigs. Asian-Aust. J. Anim. Sci., 26: 1365-1373.
Fan, B., S. Lkhagvadorj, W. Cai, J. Young and R.M. Smith et al., 2010. Identification of genetic markers associated with residual feed intake and meat quality traits in the pig. Meat. Sci., 84: 645-650.
Du, Z.Q., B. Fan, X. Zhao, R. Amoako and M.F. Rothschild, 2009. Association analysis between type 2 diabetes genes and obesity traits in pigs. Obesity (Silver Spring), 17: 323-329.
Xia, J.H., G. Lin, X. He, B. Yunping and P. Liu et al., 2014. Mapping quantitative trait loci for omega-3 fatty acids in Asian seabass. Mar. Biotechnol., 16: 1-9.
Turner, D.L. and P.J. Butler., 1988. The aerotic capacity of locomotory muscle in the tufted duck aythya fuligula. J. Exp. Biol., 135: 445-460.
Joo, S.T., G.D. Kim, Y.H. Hwang and Y.C. Ryu, 2013. Control of fresh meat quality through manipulation of muscle fiber characteristics. Meat Sci., 95: 828-836.
Li, X., M. Ekerljung, K. Lundstrom and A. Lunden, 2013. Association of polymorphisms at DGAT1, leptin, SCD1, CAPN1 and CAST genes with color, marbling and water holding capacity in meat from beef cattle populations in Sweden. Meat Sci., 94: 153-158.
Steneberg, P., A.G. Sykaras, F. Backlund, J. Straseviciene, I. Soderstrom and H. Edlund, 2015. Hyperinsulinemia enhances hepatic expression of the fatty acid transporter Cd36 and provokes hepatosteatosis and hepatic insulin resistance. J. Biol. Chem. 290: 19034-19043.
Warensjo, E., J. Sundstrom, B. Vessby, T. Cederholm and U. Riserus, 2008. Markers of dietary fat quality and fatty acid desaturation as predictors of total and cardiovascular mortality: A population-based prospective study. Am. J. Clin. Nutr., 88: 203-209.
Kashani, A., B.W.B. Holman, P.D. Nichols and A.E. Malau-Aduli, 2015. Effect of dietary supplementation with Spirulina on the expressions of AANAT, ADRB3, BTG2 and FASN genes in the subcutaneous adipose and Longissimus dorsi muscle tissues of purebred and crossbred Australian sheep. J. Anim. Sci. Technol., Vol. 57.
USDA and USDHHS., 2010. Dietary Guidelines for Americans. 7th Edn., United State Department of Agriculture and United State Department of Health and Human Services, Washington DC., USA.
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