Association analysis of mitochondrial DNA polymorphisms with oocyte number in pigs
Hao Liu A , Wenshu Shi A , Dan Wang A and Xingbo Zhao A BA College of Animal Science and Technology, China Agricultural University, No. 2 Yuanmingyuan West Road, Haidian District, Beijing 100193, P. R. China.
B Corresponding author. Email: zhxb@cau.edu.cn
Reproduction, Fertility and Development 31(4) 805-809 https://doi.org/10.1071/RD18219
Submitted: 10 June 2018 Accepted: 17 November 2018 Published: 7 January 2019
Abstract
In pigs, correlations between mitochondrial (mt) DNA polymorphisms and economic traits have been widely reported across and within swine breeds. In fecundity studies, the number of oocytes within ovaries was highly correlated with litter size. However, the effect of mitochondrial polymorphisms on porcine oocyte number remained unclear. In this study, 181 porcine ovaries were collected to analyse the relationship between oocyte number and mtDNA polymorphisms. There were considerable differences in oocyte numbers among different ovaries from commercial pig breeds, ranging from 2.7 × 105 to 1.3 × 106. Mitochondrial D-loop sequencing discovered 53 polymorphic sites. Association analysis revealed that 13 variations were associated with the number of oocytes (P < 0.05). A C323T polymorphism showed the largest value between the C and T carriers, which differed at 105 oocytes (P < 0.05). The 53 polymorphic sites generated 45 haplotypes, which clustered into two haplogroups, A and B. Haplogroup A had a higher number of oocytes than Haplogroup B (P < 0.05), whereas Haplotype H6 in Haplogroup A had the highest number of oocytes (~7.5 × 105) of all haplotypes studied (P < 0.05). The results of this study highlight a correlation between mtDNA polymorphisms and oocyte number, and suggest the potential application of mtDNA polymorphism analyses in pig selection and breeding practices.
Additional keywords: haplotype, mitochondrial D-loop, swine.
References
Aversa, R., Petrescu, R. V. V., Apicella, A., and Petrescu, F. I. T. (2016). Mitochondria are naturally micro robots – a review. Am. J. Eng. Appl. Sci. 9, 991–1002.| Mitochondria are naturally micro robots – a review.Crossref | GoogleScholarGoogle Scholar |
Babayev, E., and Seli, E. (2015). Oocyte mitochondrial function and reproduction. Curr. Opin. Obstet. Gynecol. 27, 175–181.
| Oocyte mitochondrial function and reproduction.Crossref | GoogleScholarGoogle Scholar | 25719756PubMed |
Chen, X., Wang, D., Xiang, H., Dun, W., Brahi, D. O. H., Tao, Y., and Zhao, X. (2017). Mitochondrial DNA T7719G in tRNA-Lys gene affects litter size in small-tailed Han sheep. J. Anim. Sci. Biotechnol. 8, 31.
| Mitochondrial DNA T7719G in tRNA-Lys gene affects litter size in small-tailed Han sheep.Crossref | GoogleScholarGoogle Scholar | 28405314PubMed |
Fernández, A. I., Alves, E., Fernández, A., De, P. E., López-García, M. A., Ovilo, C., Rodríguez, M. C., and Silió, L. (2008). Mitochondrial genome polymorphisms associated with longissimus muscle composition in Iberian pigs. J. Anim. Sci. 86, 1283–1290.
| Mitochondrial genome polymorphisms associated with longissimus muscle composition in Iberian pigs.Crossref | GoogleScholarGoogle Scholar | 18344306PubMed |
Gu, L., Liu, H., Gu, X., Boots, C., Moley, K. H., and Wang, Q. (2015). Metabolic control of oocyte development: linking maternal nutrition and reproductive outcomes. Cell. Mol. Life Sci. 72, 251–271.
| Metabolic control of oocyte development: linking maternal nutrition and reproductive outcomes.Crossref | GoogleScholarGoogle Scholar | 25280482PubMed |
Hiendleder, S. (1996). Molecular characterization of the sheep mitochondrial genome. J. Anim. Breed Genet. 113, 293–302.
| Molecular characterization of the sheep mitochondrial genome.Crossref | GoogleScholarGoogle Scholar |
Hu, Y. B., Pan, Z. X., Xu, D., Xu, Y. X., Liu, H. L., Huang, R. H., and Hu, Z. G. (2006). The correlation of reproduction-related gene expression with germ cell number in DM and PLL gilts. Acta Genet. Sin. 33, 800–807.
| The correlation of reproduction-related gene expression with germ cell number in DM and PLL gilts.Crossref | GoogleScholarGoogle Scholar | 16980126PubMed |
Hunter, M. G. (2000). Oocyte maturation and ovum quality in pigs. Rev. Reprod. 5, 122–130.
| Oocyte maturation and ovum quality in pigs.Crossref | GoogleScholarGoogle Scholar | 10864857PubMed |
Jones, E. C., and Krohn, P. L. (1961). The relationships between age, numbers of oocytes and fertility in virgin and multiparous mice. J. Endocrinol. 21, 469–495.
| The relationships between age, numbers of oocytes and fertility in virgin and multiparous mice.Crossref | GoogleScholarGoogle Scholar | 13790510PubMed |
King, A. H., Jiang, Z., Gibson, J. P., Haley, C. S., and Archibald, A. L. (2003). Mapping quantitative trait loci affecting female reproductive traits on porcine chromosome 81. Biol. Reprod. 68, 2172–2179.
| Mapping quantitative trait loci affecting female reproductive traits on porcine chromosome 81.Crossref | GoogleScholarGoogle Scholar | 12606397PubMed |
Knox, R. V. (2005). Recruitment and selection of ovarian follicles for determination of ovulation rate in the pig. Domest. Anim. Endocrinol. 29, 385–397.
| Recruitment and selection of ovarian follicles for determination of ovulation rate in the pig.Crossref | GoogleScholarGoogle Scholar | 15998504PubMed |
Macedo, A. A., Bittar, J. F. F., Bassi, P. B., Ronda, J. B., Bittar, E. R., Panetto, J. C. C., Araujo, M. S. S., Santos, R. L., and Martins-Filho, O. A. (2014). Influence of endogamy and mitochondrial DNA on immunological parameters in cattle. BMC Veterinary Research 10, 79.
| Influence of endogamy and mitochondrial DNA on immunological parameters in cattle.Crossref | GoogleScholarGoogle Scholar | 24694022PubMed |
McCoard, S. A., Wise, T. H., and Ford, J. J. (2003). Germ cell development in Meishan and White Composite gilts. Anim. Reprod. Sci. 77, 85–105.
| Germ cell development in Meishan and White Composite gilts.Crossref | GoogleScholarGoogle Scholar | 12654530PubMed |
Miyano, T., and Manabe, N. (2007). Oocyte growth and acquisition of meiotic competence. Soc. Reprod. Fertil. Suppl. 63, 531–538.
| 17566297PubMed |
Modina, S. C., Tessaro, I., Lodde, V., Franciosi, F., Corbani, D., and Luciano, A. M. (2014). Reductions in the number of mid-sized antral follicles are associated with markers of premature ovarian senescence in dairy cows. Reprod. Fertil. Dev. 26, 235–244.
| Reductions in the number of mid-sized antral follicles are associated with markers of premature ovarian senescence in dairy cows.Crossref | GoogleScholarGoogle Scholar | 23327793PubMed |
Qin, Y. H., Chen, S. Y., and Lai, S. J. (2012). Polymorphisms of mitochondrial ATPase 8/6 genes and association with milk production traits in Holstein cows. Anim. Biotechnol. 23, 204–212.
| Polymorphisms of mitochondrial ATPase 8/6 genes and association with milk production traits in Holstein cows.Crossref | GoogleScholarGoogle Scholar | 22870875PubMed |
Shields, R. G., Mahan, D. C., and Maxson, P. F. (1985). Effect of dietary gestation and lactation protein levels on reproductive performance and body composition of first-litter female swine. J. Anim. Sci. 60, 179–189.
| Effect of dietary gestation and lactation protein levels on reproductive performance and body composition of first-litter female swine.Crossref | GoogleScholarGoogle Scholar | 3972739PubMed |
Sutarno, , Cummins, J. M., Greeff, J., and Lymbery, A. J. (2002). Mitochondrial DNA polymorphisms and fertility in beef cattle. Theriogenology 57, 1603–1610.
| Mitochondrial DNA polymorphisms and fertility in beef cattle.Crossref | GoogleScholarGoogle Scholar | 12035972PubMed |
Tsai, T.-S., Rajasekar, S., and St. John, J. C. (2016). The relationship between mitochondrial DNA haplotype and the reproductive capacity of domestic pigs (Sus scrofa domesticus). BMC Genet. 17, 67.
| The relationship between mitochondrial DNA haplotype and the reproductive capacity of domestic pigs (Sus scrofa domesticus).Crossref | GoogleScholarGoogle Scholar | 27188709PubMed |
Vakifahmetoglu-Norberg, H., Ouchida, A. T., and Norberg, E. (2017). The role of mitochondria in metabolism and cell death. Biochem. Biophys. Res. Commun. 482, 426–431.
| The role of mitochondria in metabolism and cell death.Crossref | GoogleScholarGoogle Scholar | 28212726PubMed |
Wang, C., Wang, H., Zhang, Y., Tang, Z., Li, K., and Liu, B. (2015). Genome-wide analysis reveals artificial selection on coat colour and reproductive traits in Chinese domestic pigs. Mol. Ecol. Resour. 15, 414–424.
| Genome-wide analysis reveals artificial selection on coat colour and reproductive traits in Chinese domestic pigs.Crossref | GoogleScholarGoogle Scholar | 25132237PubMed |
Yeste, M. (2016). Introduction to the special issue on swine reproduction. Theriogenology 85, 2–3.
| Introduction to the special issue on swine reproduction.Crossref | GoogleScholarGoogle Scholar | 26518134PubMed |
Yeung, K. Y., Dickinson, A., Donoghue, J. F., Polekhina, G., White, S. J., Grammatopoulos, D. K., McKenzie, M., Johns, T. G., and St. John, J. C. (2014). The identification of mitochondrial DNA variants in glioblastoma multiforme. Acta Neuropathol. Commun. 2, 1.
| The identification of mitochondrial DNA variants in glioblastoma multiforme.Crossref | GoogleScholarGoogle Scholar | 24383468PubMed |
Zhang, C. L., Wang, Y. H., Xie, M., Chen, M., Wang, X. H., and Hou, S. S. (2012). Mitochondrial coding gene polymorphisms associated with carcass traits in Beijing duck. J. Anim. Vet. Adv. 9, 2522–2525.