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High-density single nucleotide polymorphism chip-based conservation genetic analysis of indigenous pig breeds from Shandong Province, China

  • Wang, Yanping (Shandong Provincial Key Laboratory of Animal Disease Control and Breeding, Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Sciences) ;
  • Zhao, Xueyan (Shandong Provincial Key Laboratory of Animal Disease Control and Breeding, Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Sciences) ;
  • Wang, Cheng (Shandong Provincial Key Laboratory of Animal Disease Control and Breeding, Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Sciences) ;
  • Wang, Wenwen (Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, College of Animal Science and Technology, Shandong Agricultural University) ;
  • Zhang, Qin (Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, College of Animal Science and Technology, Shandong Agricultural University) ;
  • Wu, Ying (Shandong Provincial Key Laboratory of Animal Disease Control and Breeding, Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Sciences) ;
  • Wang, Jiying (Shandong Provincial Key Laboratory of Animal Disease Control and Breeding, Institute of Animal Science and Veterinary Medicine, Shandong Academy of Agricultural Sciences)
  • Received : 2020.03.16
  • Accepted : 2020.10.18
  • Published : 2021.07.01

Abstract

Objective: Shandong indigenous pig breeds are important Chinese pig resources. Their progressive population decline in recent decades has attracted attention towards their conservation. Conservation genetics of these indigenous breeds are essential for developing a conservation and utilization scheme. Methods: A high-density single nucleotide polymorphism (HD-SNP) chip-based comparative analysis of genetic characteristics was performed for seven Shandong indigenous pig breeds in the context of five Western commercial breeds. Results: The results showed that Shandong indigenous pig breeds varied greatly in genetic diversity, effective population size, inbreeding level, and genetic distance with the Western commercial breeds. Specifically, Laiwu and Dapulian displayed low genetic diversity, and had a genetically distant relationship with the Western commercial breeds (average F statistics [FST] value of 0.3226 and 0.2666, respectively). Contrastingly, the other five breeds (Yantai, Licha, Yimeng, Wulain, and Heigai) displayed high genetic diversity within breed and had some extent of mixture pattern with the Western commercial breeds, especially Duroc and Landrace (FST values from 0.1043 to 0.2536). Furthermore, intensive gene flow was discovered among the seven Shandong indigenous breeds, particularly Wulian, Licha, and Heigai, as indicated by the large cluster formed in the principal component analysis scatterplot and small population differentiation (average of 0.1253) among them. Conclusion: Our study advances the understanding of genetic characteristics of Shandong indigenous breeds and provides essential information for developing an appropriate conservation and utilization scheme for these breeds.

Keywords

Acknowledgement

The authors would like to acknowledge the conservation farms of seven Shandong indigenous pig breeds and breeding farms of five Western commercial pig breeds for providing pig samples. We also would like to thank Editage (www. editage.cn) for English language editing. This research was supported by the Natural Science Foundations of Shandong Province (ZR2017MC043), Shandong Swine Industry Technology System Innovation (SDAIT-08-03), and Agricultural Improved Variety Engineering of Shandong (2019LZGC019).

References

  1. Agri Benchmark. Pig report. Understanding agriculture worldwide. 2018.
  2. National Commission of Animal Genetic Resources of China. Animal genetic resources in China: pigs. Beijing, China: China Agriculture Press; 2011.
  3. Si J, Zhang H, Tang J. Livestock breeds in Shandong province. Shenzhen, China: Haitian Press; 1999.
  4. Wang H, Wang J, Yang D, Liu Z, Zeng Y, Chen W. Expression of lipid metabolism genes provides new insights into intramuscular fat deposition in Laiwu pigs. Asian-Australas J Anim Sci 2020;33:390-7. https://doi.org/10.5713/ajas.18.0225
  5. Chen W, Fang G, Wang S, Wang H, Zeng Y. Longissimus lumborum muscle transcriptome analysis of Laiwu and Yorkshire pigs differing in intramuscular fat content. Genes Genomics 2017;39:759-66. https://doi.org/10.1007/s13258017-0540-9
  6. Xing J, Xing F, Zhang C, et al. Genome-wide gene expression profiles in lung tissues of pig breeds differing in resistance to porcine reproductive and respiratory syndrome virus. PLoS One 2014;9:e86101. https://doi.org/10.1371/journal.pone.0086101
  7. Jiang C, Xing F, Xing J, Jiang Y, Zhou E. Different expression patterns of PRRSV mediator genes in the lung tissues of PRRSV resistant and susceptible pigs. Dev Comp Immunol 2013;39:127-31. https://doi.org/10.1016/j.dci.2012.01.003
  8. Yang G, Ren J, Zhang Z, Huang L. Genetic evidence for the introgression of Western NR6A1 haplotype into Chinese Licha breed associated with increased vertebral number. Anim Genet 2009;40:247-50. https://doi.org/10.1111/j.13652052.2008.01820.x
  9. Megens HJ, Crooijmans RP, San Cristobal M, Hui X, Li N, Groenen MA. Biodiversity of pig breeds from China and Europe estimated from pooled DNA samples: differences in microsatellite variation between two areas of domestication. Genet Sel Evol 2008;40:103. https://doi.org/10.1186/12979686-40-1-103
  10. Fenster CB, Ballou JD, Dudash MR, et al. Conservation and genetics. Yale J Biol Med 2018;91:491-501.
  11. Frankham R, Ralls K. Inbreeding leads to extinction. Nature 1998;392:441-2. https://doi.org/10.1038/33022
  12. Lu P, Li D, Yin J, Zhang L, Wang Z. Flavour differences of cooked longissimus muscle from Chinese indigenous pig breeds and hybrid pig breed (Duroc×Landrace×Large White). Food Chem 2008;107:1529-37. https://doi.org/10.1016/j.foodchem.2007.10.010
  13. Wang JY, Guo JF, Zhang Q, et al. Genetic diversity of Chinese indigenous pig breeds in Shandong province using microsatellite markers. Asian-Australas J Anim Sci 2011;24:28-36. https://doi.org/10.5713/ajas.2011.10091
  14. Wang J, Guo J, Hao X, et al. Phylogenetic relationships of pig breeds from Shandong province of China and their influence by modern commercial breeds by analysis of mitochondrial DNA sequences. Ital J Anim Sci 2010;9:e48.
  15. Peripolli E, Munari DP, Silva MVGB, Lima ALF, Irgang R, Baldi F. Runs of homozygosity: current knowledge and applications in livestock. Anim Genet 2017;48:255-71. https://doi.org/10.1111/age.12526
  16. Zhan H, Zhang S, Zhang K, et al. Genome-wide patterns of homozygosity and relevant characterizations on the population structure in Pietrain pigs. Genes 2020;11:577. https://doi.org/10.3390/genes11050577
  17. Schiavo G, Bovo S, Bertolini F, et al. Comparative evaluation of genomic inbreeding parameters in seven commercial and autochthonous pig breeds. Animal 2020;14:910-20. https://doi.org/10.1017/S175173111900332X
  18. Herrero-Medrano JM, Megens HJ, Groenen MA, et al. Conservation genomic analysis of domestic and wild pig populations from the Iberian Peninsula. BMC Genet 2013;14:106. https://doi.org/10.1186/1471-2156-14-106
  19. Ai H, Huang L, Ren J. Genetic diversity, linkage disequilibrium and selection signatures in Chinese and Western pigs revealed by genome-wide SNP markers. PLoS One 2013;8:e56001. https://doi.org/10.1371/journal.pone.0056001
  20. Munoz M, Bozzi R, Garcia-Casco J, et al. Genomic diversity, linkage disequilibrium and selection signatures in European local pig breeds assessed with a high density SNP chip. Sci Rep 2019;9:13546. https://doi.org/10.1038/s41598-01949830-6
  21. Qin M, Li C, Li Z, Chen W, Zeng Y. Genetic diversities and differentially selected regions between Shandong indigenous pig breeds and Western pig breeds. Front Genet 2020;10:1351. https://doi.org/10.3389/fgene.2019.01351
  22. Sambrook J, Russell DW. Molecular cloning: a laboratory manual. 3rd ed. New York, NY, USA: Cold Spring Harbor Laboratory Press; 2001.
  23. 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
  24. McQuillan R, Leutenegger AL, Abdel-Rahman R, et al. Runs of homozygosity in European populations. Am J Hum Genet 2008;83:359-72. https://doi.org/10.1016/j.ajhg.2008.08.007
  25. Sved JA. Linkage disequilibrium and homozygosity of chromosome segments in finite populations. Theor Popul Biol 1971;2:125-41. https://doi.org/10.1016/0040-5809(71)90011-6
  26. Tortereau F, Servin B, Frantz L, et al. A high density recombination map of the pig reveals a correlation between sex-specific recombination and GC content. BMC Genomics 2012;13:586. https://doi.org/10.1186/1471-2164-13-586
  27. Hayes BJ, Visscher PM, McPartlan HC, Goddard ME. Novel multilocus measure of linkage disequilibrium to estimate past effective population size. Genome Res 2003;13:635-43. https://doi.org/10.1101/gr.387103
  28. Alexander DH, Novembre J, Lange K. Fast model-based estimation of ancestry in unrelated individuals. Genome Res 2009;19:1655-64. https://doi.org/10.1101/gr.094052.109
  29. Weir BS, Cockerham CC. Estimating F-statistics for the analysis of population structure. Evolution 1984;38:1358-70. https://doi.org/10.2307/2408641
  30. Tajima F, Nei M. Estimation of evolutionary distance between nucleotide sequences. Mol Biol Evol 1984;1:269-85. https://doi.org/10.1093/oxfordjournals.molbev.a040317
  31. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987;4:406-25. https://doi.org/10.1093/oxfordjournals.molbev.a040454
  32. Kumar S, Stecher G, Tamura K. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 2016;33:1870-4. https://doi.org/10.1093/molbev/msw054
  33. Ramos AM, Crooijmans RP, Affara NA, et al. Design of a high density SNP genotyping assay in the pig using SNPs identified and characterized by next generation sequencing technology. PLoS One 2009;4:e6524. https://doi.org/10.1371/journal.pone.0006524
  34. Quan J, Gao C, Cai Y, Ge Q, Jiao T, Zhao S. Population genetics assessment model reveals priority protection of genetic resources in native pig breeds in China. Glob Ecol Conserv 2020;21:e00829. https://doi.org/10.1016/j.gecco.2019.e00829
  35. Sato K, Sato M. Multiple ways to prevent transmission of paternal mitochondrial DNA for maternal inheritance in animals. J Biochem 2017;162:247-53. https://doi.org/10.1093/jb/mvx052
  36. Zuidema D, Sutovsky P. The domestic pig as a model for the study of mitochondrial inheritance. Cell Tissue Res 2020;380:263-71. https://doi.org/10.1007/s00441-019-03100-z
  37. Badke YM, Bates RO, Ernst CW, Schwab C, Steibel JP. Estimation of linkage disequilibrium in four US pig breeds. BMC Genomics 2012;13:24. https://doi.org/10.1186/14712164-13-24
  38. Uimari P, Tapio M. Extent of linkage disequilibrium and effective population size in Finnish Landrace and Finnish Yorkshire pig breeds. J Anim Sci 2011;89:609-14. https://doi.org/10.2527/jas.2010-3249
  39. Purfield DC, Berry DP, McParland S, Bradley DG. Runs of homozygosity and population history in cattle. BMC Genet 2012;13:70. https://doi.org/10.1186/1471-2156-13-70
  40. Meuwissen TH. Accuracy of breeding values of 'unrelated' individuals predicted by dense SNP genotyping. Genet Sel Evol 2009;41:35. https://doi.org/10.1186/1297-9686-41-35
  41. Wright S. Isolation by distance. Genetics 1943;28:114-38. https://doi.org/10.1093/genetics/28.2.114
  42. Hartl DL, Clark AG. Principles of population genetics. 3rd ed. Sunderland, MA, USA: Sinauer Associates Inc.; 1997.