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Evaluation of genetic differentiation and search for candidate genes for reproductive traits in pigs

  • Elena Romanets (Faculty of Biotechnology, Don State Agrarian University) ;
  • Siroj Bakoev (Faculty of Biotechnology, Don State Agrarian University) ;
  • Timofey Romanets (Faculty of Biotechnology, Don State Agrarian University) ;
  • Maria Kolosova (Faculty of Biotechnology, Don State Agrarian University) ;
  • Anatoly Kolosov (Faculty of Biotechnology, Don State Agrarian University) ;
  • Faridun Bakoev (Faculty of Biotechnology, Don State Agrarian University) ;
  • Olga Tretiakova (Faculty of Biotechnology, Don State Agrarian University) ;
  • Alexander Usatov (Academy of Biology and Biotechnology named after. DI. Ivanovsky, Southern Federal University) ;
  • Lyubov Getmantseva (Faculty of Biotechnology, Don State Agrarian University)
  • Received : 2023.08.11
  • Accepted : 2023.11.22
  • Published : 2024.05.01

Abstract

Objective: The use of molecular genetic methods in pig breeding can significantly increase the efficiency of breeding and breeding work. We applied the Fst (fixsacion index) method, the main focus of the work was on the search for common options related to the number of born piglets and the weight of born piglets, since today the urgent task is to prevent a decrease in the weight of piglets at birth while maintaining high fertility of sows. Methods: One approach is to scan the genome, followed by an assessment of Fst and identification of selectively selected regions. We chose Large White sows (n = 237) with the same conditions of keeping and feeding. The data were collected from the sows across three farrowing. For genotyping, we used GeneSeek GGP Porcine HD Genomic Profiler v1, which included 68,516 single nucleotide polymorphisms evenly distributed with an average spacing of 25 kb (Illumina Inc, San Diego, CA, USA). Results: Based on the results of the Fst analysis, 724 variants representing selection signals for the signs BALWT, BALWT1, NBA, and TNB (weight of piglets born alive, average weight of the 1st piglets born alive, total number born alive, total number born). At the same time, 18 common variants have been identified that are potential markers for both the number of piglets at birth and the weight of piglets at birth, which is extremely important for breeding work to improve reproductive characteristics in sows. Conclusion: Our work resulted in identification of variants associated with the reproductive characteristics of pigs. Moreover, we identified, variants which are potential markers for both the number of piglets at birth and the weight of piglets at birth, which is extremely important for breeding work to improve reproductive performance in sows.

Keywords

Acknowledgement

This work was supported by the Russian Science Foundation grant no. 22-76-10015.

References

  1. Yang W, Kang X, Yang Q, Lin Y, Fang M. Review on the development of genotyping methods for assessing farm animal diversity. J Anim Sci Biotechnol 2013;4:2. https://doi.org/10.1186/2049-1891-4-2 
  2. Ding N, Guo Y, Knorr C, et al. Genome-wide QTL mapping for three traits related to teat number in a White Duroc × Erhualian pig resource population. BMC Genet 2009;10:6. https://doi.org/10.1186/1471-2156-10-6 
  3. Getmantseva L, Kolosova M, Bakoev F, Zimina A, Bakoev S. Genomic regions and candidate genes linked to capped hock in pig. Life (Basel), 2021;11:510. https://doi.org/10.3390/life11060510
  4. Cai Z, Lund OF, Lund MS, Ostersen T, Sahana G. Large-scale association study on daily weight gain in pigs reveals overlap of genetic factors for growth in humans. BMC Genomics 2022;23:133. https://doi.org/10.1186/s12864-022-08373-3 
  5. Subramanian S. The difference in the proportions of deleterious variations within and between populations influences the estimation of FST. Genes (Basel) 2022;13:194. https://doi.org/10.3390/genes13020194
  6. Kunhareang S, Zhou H, Hickford JGH. Rapid DNA extraction of pig ear tissues. Meat Sci 2010;85:589-90. https://doi.org/10.1016/j.meatsci.2010.02.028 
  7. Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81:559-75. https://doi.org/10.1086/519795 
  8. Weir BS, Cockerham CC. Estimating f-statistics for the analysis of population structure. Evolution 1984;38:135870. https://doi.org/10.1111/j.1558-5646.1984.tb05657.x 
  9. Bergfelder-Druing S, Grosse-Brinkhaus C, Lind B, et al. A genome-wide association study in large white and landrace pig populations for number piglets born alive. PLoS One 2015;10:e0117468. https://doi.org/10.1371/journal.pone.0117468 
  10. He LC, Li PH, Ma X, et al. Identification of new single nucleotide polymorphisms affecting total number born and candidate genes related to ovulation rate in Chinese Erhualian pigs. Anim Genet 2017;48:48-54. https://doi.org/10.1111/age.12492 
  11. Lindholm-Perry AK, Freetly HC, Oliver WT, Rempel LA, Keel BN. Genes associated with body weight gain and feed intake identified by meta-analysis of the mesenteric fat from crossbred beef steers. PLoS One 2020;15:e0227154. https://doi.org/10.1371/journal.pone.0227154 
  12. Dolebo AT, Khayatzadeh N, Melesse A, et al. Genome-wide scans identify known and novel regions associated with prolificacy and reproduction traits in a sub-Saharan African indigenous sheep (Ovis aries). Mamm Genome 2019;30:339-52. https://doi.org/10.1007/s00335-019-09820-5 
  13. Schneider JF, Nonneman DJ, Wiedmann RT, Vallet JL, Rohrer GA. Genomewide association and identification of candidate genes for ovulation rate in swine. J Anim Sci 2014;92:3792-803. https://doi.org/10.2527/jas.2014-7788 
  14. Rohrer GA, Wise TH, Lunstra DD, Ford JJ. Identification of genomic regions controlling plasma FSH concentrations in Meishan-White Composite boars. Physiol Genomics 2001;28:6:145-51. https://doi.org/10.1152/physiolgenomics.2001.6.3.145 
  15. de Koning DJ, Rattink AP, Harlizius B, Groenen MAM, Brascamp EW, van Arendonk JAM. Detection and characterization of quantitative trait loci for growth and reproduction traits in pigs. Livest Prod Sci 2001;72:185-98. https://doi.org/10.1016/S0301-6226(01)00226-3 
  16. Ai H, Ren J, Zhang Z, et al. Detection of quantitative trait loci for growth- and fatness-related traits in a large-scale White Duroc × Erhualian intercross pig population. Anim Genet 2012;43:4:383-91. https://doi.org/10.1111/j.1365-2052.2011.02282.x 
  17. Symoens S, Barnes AM, Gistelinck C, et al. Genetic defects in TAPT1 disrupt ciliogenesis and cause a complex lethal osteochondrodysplasia. Am J Hum Genet 2015;97:521-34. https://doi.org/10.1016/j.ajhg.2015.08.009 
  18. Zhang L, Wang F, Gao G, et al. genome-wide association study of body weight traits in inner mongolia cashmere goats. Front Vet Sci 2021;8:752746. https://doi.org/10.3389/fvets.2021.752746 
  19. Kudo LC, Parfenova L, Ren G, et al. Puromycin-sensitive aminopeptidase (PSA/NPEPPS) impedes development of neuropathology in hPSA/TAUP301L double-transgenic mice. Hum Mol Genet 2011;20:1820-33. https://doi.org/10.1093/hmg/ddr065 
  20. Towne CF, York IA, Neijssen J, et al. Puromycin-sensitive aminopeptidase limits MHC class I presentation in dendritic cells but does not affect CD8 T cell responses during viral infections. J Immunol 2008;180:1704-12. https://doi.org/10.4049/jimmunol.180.3.1704 
  21. Guo YM, Lee GJ, Archibald AL, Haley CS. Quantitative trait loci for production traits in pigs: a combined analysis of two Meishan x Large White populations. Anim Genet 2008;39:486-95. https://doi.org/10.1111/j.1365-2052.2008.01756.x 
  22. Sato S, Atsuji K, Saito N, et al. Identification of quantitative trait loci affecting corpora lutea and number of teats in a Meishan × Duroc F2 resource population. J Anim Sci 2006;84:11:2895-901. https://doi.org/10.2527/jas.2006-176 
  23. Ding R, Zhuang Z, Qiu Y, et al. A composite strategy of genome-wide association study and copy number variation analysis for carcass traits in a Duroc pig population. BMC Genomics 2022;23:590. https://doi.org/10.1186/s12864-022-08804-1 
  24. Karlsson M, Sjostedt E, Oksvold P, et al. Genome-wide annotation of protein-coding genes in pig. BMC Biol 2022;20:25. https://doi.org/10.1186/s12915-022-01229-y 
  25. Durkin ME, Yuan BZ, Zhou X, et al. DLC-1:a Rho GTPase-activating protein and tumour suppressor. J Cell Mol Med 2007;11:1185-207. https://doi.org/10.1111/j.1582-4934. 2007.00098.x 
  26. Okitsu Y, Nagano M, Yamagata T, et al. DLEC1 is required for spermatogenesis and male fertility in mice. Sci Rep 2020;10:18883. https://doi.org/10.1038/s41598-020-75957-y 
  27. Sabbir M, Wigle N, Loewen S, et al. Identification and characterization of Dlc1 isoforms in the mouse and study of the biological function of a single gene trapped isoform. BMC Biol 2010;8:17. https://doi.org/10.1186/1741-7007-8-17 
  28. Bakoev S, Getmantseva L, Kostyunina O, et al. Genome-wide analysis of genetic diversity and artificial selection in Large White pigs in Russia. PeerJ 2021;9:e11595. https://doi.org/10.7717/peerj.11595