Investigation on single nucleotide polymorphism of BMPR1B and GDF9 genes in Mughani, Afshari and Baluchi ewes

Authors

1 Assistant Professor, Department of Animal Science, Faculty of Agriculture and Animal Husbandry, Torbat Jam Higher Education Complex

2 Associate Professor, Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad

3 Associate Professor, Agricultural and Horticultural Science Research Department, Khorasan Razavi Agricultural and Natural Resources Research and Education Center, Mashhad,

Abstract

Sheep are used as a genetic model to study the relationship between genetic diversity and ovulation rate. Previous studies have shown that ovulation rate and litter size can be controlled by a set of genes called fecundity genes . Three fertility genes have been identified in sheep called BMPR1B or FecB, GDF9 or FecG and BMP15 or FecX. Tetra-ARMS-PCR is a suitable alternative method in the context of expensive methods such as sequencing and PCR-RFLP to identify SNPs whose sequences are known. The entry of the Booroola allele into the Afshari breed increased the frequency of litter size. The aim of this study was to investigate the polymorphism of two fertility genes including FecB and FecG in Mughani, Afshari and Baluchi sheep in Khorasan Razavi province.
Blood samples were taken from 95 Afshari, Baluchi and Mughani sheep. Two pairs of control (outer) and specific (inner) primers were used to amplify FecB and FecG gene fragments by the Tetra-ARMS PCR method. Temperature cycling of PCR amplification for FecB started at 94°C for 4 minutes, followed by 35 cycles consisting of 94°C for 25 seconds, annealing temperature at 54°C for 35 seconds, extension at 72°C for 20 seconds and a final extension at 72°C for 5 minutes. For amplification of the G1 point mutation on the FecG gene, the annealing temperature was 54°C for 35 s, extension was 70°C for 40 s, and final extension was 70°C for 5 minutes. The PCR products were electrophoresed on a 2% agarose gel.
Three genotypes have been observed for the FecB gene in Afshari sheep; wild homozygous (++), heterozygous (B+) and homozygous mutant (BB). All Mughani and Baluchi sheep were homozygous for this gene. A 108 bp band was detected for mutant homozygotes. A band of 213 bp was observed in wild homozygotes. The frequency of wild homozygotes was high in the three breeds,. The frequency of the wild allele in this breed was 0.39 and that of the mutant allele 0.61, the overall frequencies for the three breeds being 0.8 and 0.2, respectively. The result of Tetra-ARMS-PCR for the G1 point mutation of the GDF9 gene showed polymorphism in all three breeds, however, the frequency of wild homozygotes was high. In the Balochi breed, only two animals (4%) were heterozygous and 96% of the animals showed the wild homozygous genotype. In the Mughani breed, 16% were heterozygous and only one animal was homozygous mutant. In addition, only one heterozygote was observed in the Afshari breed. Several studies have shown the association of the FecB, FecG and FecX genes with litter size in sheep. Due to the high frequency of wild homozygotes and the fact that Mughani and Baluchi ewes mostly gave birth to single lambs, the role of FecB mutation in litter size of Afshari ewes was observed. The ram used in this herd was heterozygous for FecB. In general, it can be concluded that the mutant FecB allele has a correlation with litter size in Iranian sheep. However, the statistical confirmation of this issue requires a dedicated study with a detailed record of reproductive traits.
The results of this study demonstrated the presence of a Booroola mutation in the Afshari ewes that were offspring of heterozygous rams. In addition, all of these ewes had litter size in at least one of the two pregnancies. Hence, the Booroola mutation may potentially increase the litter size of ewes. However, a more comprehensive study measuring biological indicators such as sex hormone levels, ovulation rate and follicle size is needed to demonstrate the effect of these types of mutations on increasing fertility.

Keywords

Main Subjects


  1.  Aboelhassan, D.M., Darwish, A.M., Ali, N.I., Ghaly, I.S. and Farag, I.M. 2021. A study on mutation points of GDF9 gene and their association with prolificacy in Egyptian small ruminants. Journal of Genetic Engineering and Biotechnology, 19: 85.

    Ahlawat, S., Sharma, R., Maitra, A., Roy, M. and Tantia, M.S. 2014. Designing, optimization and validation of tetra-primer ARMS PCR protocol for genotyping mutations in caprine Fec genes. Meta Gene, 2: 439–49.

    Barzegari, A., Atashpaz, S., Ghabili, K., Nemati, Z., Mohseniazar, M. and Azarbaijani, R. 2009. Polymorphisms in GDF9 and BMP15 associated with fertility and ovulation rate in Moghani and Ghezel sheep in Iran. Reproduction in Domestic Animals, 45: 666–669.

    Bodin, L., Di Pasquale, E., Fabre, S.P., Bontoux, M., Monget, P., Persani, L. and Mulsant, P. 2007. A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep. Endocrinology, 148: 393–400.

    Chong, Y., Liu, G. and Jiang, X. 2019. Effect of BMPRIB gene on litter size of sheep in China: A meta-analysis. Animal Reproduction Science, 210: 106175.

    Davis, G.H., Montgomery, G.W., Allison, A.J., Kelly, R.W., and Bray, A.R. 1982. Segregation of a major gene influencing fecundity in progeny of Booroola sheep. New Zealand Journal of Agricultural Research, 25: 525–529.

    Davis, G.H., Dodds, K.G. and Bruce, G.D. 1999. Combined effect of the Inverdale and Booroola prolificacy genes on ovulation rate in sheep. Proceedings of the Association for the Advancement of Animal Breeding Genetics, 13: 1374–77.

    Davis, G.H., Dodds, K.G., Wheeler, R. and Jay, N. P. 2001. Evidence that an imprinted gene on the X chromosome increases ovulation rate in sheep. Biology of Reproduction, 64: 216–221.

    Davis G.H. 2005. Major genes affecting ovulation rate in sheep. Genetics Selection Evolution, 37: (Suppl 1), S11–S23.

    Eghbal Saeid, Sh., Toghyani, M., Ghaedi, K. and Nasr Esfehani, M.H. 2010. Investigating major genes affecting ovulation and multiple birth in sheep. Genetics in the 3rd Millennium, 8: 2169–2189. https://www.sid.ir/paper/117204/fa. (In Persian).

    Eghbalsaied S, Ghaedi K, Shahmoradi S, Pirestani A, Amini H, Saiedi T, Nicol L and McNeilly A. 2012. Presence of SNPs in GDF9 mRNA of Iranian Afshari sheep. International Journal of Fertility and Sterility, 5: 225–30.

    Esmail Khanian, S., Negati Javaremi, A., Afraz, F., Daneshyar, P. and Ghanbari, S. 2007. Genetic variation among Baluchi sheep population using microsatellite markers. Journal of Water and Soil Science, 11: 373–380. (In Persian).

    Fabre, S., Pierre, A., Mulsant, P., Bodin, L., Di Pasquale, E., Persani, L., Monget, P. and Monniaux, D. 2006. Regulation of ovulation rate in mammals: contribution of sheep genetic models. Reproductive Biology and Endocrinology, RB&E, 4: 20.

    Farrell, L., Creighton, P., Bohan, A., McGovern, F. and McHugh, N. 2022. Bio-economic modelling of sheep meat production systems with varying flock litter size using field data. Animal, 16: 100640.

    Ghaffari, M., Nejati Javaremi, A. and Rahimi-Mianji, G. 2009. Detection of polymorphism in BMPR-IB gene associated with twining in Shal sheep using PCR-RFLP method. International Journal of Agriculture and Biology, 11: 97–99.

    Galloway, S.M., McNatty, K.P., Cambridge, L.M., Laitinen, M.P., Juengel, J.L., Jokiranta, T.S., McLaren, R.J., Luiro, K., Dodds, K.G., Montgomery, G.W., Beattie, A.E., Davis, G.H. and Ritvos, O. 2000. Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner. Nature Genetics, 25: 279–283.

    Gholipour, R., Danesh, L., Mohammad, M. and Harkinezhad, T. 2016. Study of BMP 15 gene in Afshari and Afshari × Booroola Merino cross sheep. Iranian Journal of Animal Science Research, 7: 498–503. (In Persian).

    Gholizadeh, M. and Esmaeili-Fard, S.M. 2022. Meta-analysis of genome-wide association studies for litter size in sheep. Theriogenology, 180: 103–112.

    Guan, F., Liu, S.R., Shi, G.Q. and Yang, L.G. 2007. Polymorphism of FecB gene in nine sheep breeds or strains and its effects on litter size, lamb growth and development. Animal Reproduction Science, 99: 44–52.

    Hanrahan, J.P., Gregan, S.M., Mulsant, P., Mullen, M., Davis, G.H., Powell, R. and Galloway, S.M. 2004. Mutations in the genes for oocyte-derived growth factors GDF9 and BMP15 are associated with both increased ovulation rate and sterility in Cambridge and Belclare sheep (Ovis aries). Biology of Reproduction, 70: 900–909.

    Khanahmadi, A., Rahimi Mianji, Gh., Hafezian, S.H., Khataminejad, R., Mamizadeh, N. and Mosavi, S. M. 2016. Effect of polymorphisms in some candidate genes on twinning in cross breeds of Shall and Romanov. Research on Animal Production, 7: 192–186. (In Persian).

    Khodabakhshzadeh, R., Mohammad Abadi, M., Esmaili zadeh kashkuei, A., Moradi Shahrebabak, H. and Ansari Namin, S. 2014. Study of mutations available in first-halfexon 2 of GDF9 gene in crossbred sheep born from crossing of Romanov rams with Kermani ewes. Iranian Journal of Animal Science Research, 6: 395–403.

    Kumar, S., Dahiya, S., Magotra, A. and Kumar, S. 2017. Genetic markers associated with fecundity in sheep. International Journal of Science, Environment and Technology, 6: 3064–3074.

    Li, H., Xu, H., Akhatayeva, Z., Liu, H., Lin, C., Han, X., Lu, X., Lan, X., Zhang, Q. and Pan, C. 2021. Novel indel variations of the sheep FecB gene and their effects on litter size. Gene, 767: 145176.

    McNatty, K.P., Heath, D.A., Clark, Z., Reader, K., Juengel, J.L. and Pitman, J.L. 2017. Ovarian characteristics in sheep with multiple fecundity genes. Reproduction, 153: 233–240.

    Mohammadi, F., Saghi, D.A. and Simaie Soltani, L. 2022. Detection of FecB gene polymorphisms in sheep using rapid and low-cost tetra-ARMS PCR. Animal Sciences Journal, 34: 147–156. (In Persian).

    Montgomery, G.W., Galloway, S.M., Davis, G.H. and McNatty, K.P. 2001. Genes controlling ovulation rate in sheep. Reproduction, 121: 843–52.

    Moradband, F., Rahimi-Mianji, G. and Gholizadeh, M. 2011. Association of polymorphisms in fecundity genes of GDF9, BMP15 and BMP15-1B with litter size in Iranian Baluchi sheep. Asian-Australasian Journal of Animal Sciences, 24: 1179–1183.

    Muhaghegh Dolatabady, M. and Habibizad, J. 2019. Single nucleotide polymorphisms (SNPs) of GDF9 gene in Bahmaei and Lak Ghashghaei sheep breeds and its association with litter size. Iranian Journal of Applied Animal Science, 9: 427–432.

    Najafabadi, H.A. 2019. Investigation of variation in genes influencing fertility in New Zealand sheep. A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of Philosophy at Lincoln University.

    Newton, C.R., Graham, A., Heptinstall, L.E., Powell, S.J., Summers, C., Kalsheker, N., Smith, J.C. and Markham, A.F. 1989. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Research, 17: 2503–16.

    Polley, S., De, S., Brahma, B., Mukherjee, A., Vinesh, P.V., Batabyal, S., Arora, J.S., Pan, S., Samanta, A. K., Datta, T.K. and Goswami, S.L. 2010. Polymorphism of BMPR1B, BMP15 and GDF9 fecundity genes in prolific Garole sheep. Tropical Animal Health and Production, 42: 985–993.

    Pourtahmasebian Ahrabi, M., Eskandarinasab, M.P. and Zandi Baghcheh Maryam, M.B. 2020. Estimation of genetic parameters and genetic trend of litter size in under selection flock of Afshari sheep. Animal Production Research, 9: 23–35. (In Persian).

    Qanbarii, S., Osfoori, R. and Eskandari Nasab, M.P. 2009. Introgression of FecB major gene into elite breeding flock of Afshari sheep: preliminary evaluation of polymorphism content and applicability of marker data. Iranian Journal of Animal Science, 39: 39–47. (In Persian).

    Rajaei Nejad, M., Ayatollahi Mehrgardi, A., Vahideh, R. and Ali, E. 2020. Allelic polymorphism of exon 2 in BMP15 gene in F1 crossbred sheep from crossing Romanov rams with Kermani ewes. Journal of Livestock Science and Technologies, 8: 37–44.

    Savar sofla, S., Seyedabadi, H.R. and Javanrouh Aliabad, A. 2015. Detection of polymorphism in FecB and BMP15 candidate genes associated with litter size in Moghani flock. Animal Sciences Journal, 28, 83–90. (In Persian).

    Shafieiyan, Z., Mohammadi, G., Jolodarzadeh, A. and Amiri, S. 2013. No mutations of FecB and FecG(H) in Iranian Lory sheep. Veterinary Research Forum, 4: 265–268.

    Souza, C.J., MacDougall, C., Campbell, B.K., McNeilly, A.S. and Baird, D.T. 2001. The Booroola (FecB) phenotype is associated with a mutation in the bone morphogenetic receptor type 1 B (BMPR1B) gene. The Journal of Endocrinology, 169: R1–R6.

    1. (2019). World Population Prospects 2019. United Nations, Department of Economic and Social Affairs, Population Division (custom data acquired via website).