Journals / Turkish Journal of Veterinary and Animal Sciences / 2013 / Cilt: 37 - Sayı: 2

Application of PCR-RFLP technique to determine Booroola gene polymorphism in the Sangsari sheep breed of Iran

Pages
129–133
Publication Date
2013-02-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results obtained in this study revealed that only the wild-type allele (+) was observed in the samples, indicating that, most likely, only genotype ++ was present in the population under consideration.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Phenotypic evaluation and the culling of candidate animals for traits by applying traditional animal breeding are usually costly tasks, which need to be carried out over a considerable span of time.
📊
Key Findings & Data:Selection based upon markers could result in increased accuracy as well as a better selection response of animals.
💡
Conclusion & Impact:The results obtained in this study revealed that only the wild-type allele (+) was observed in the samples, indicating that, most likely, only genotype ++ was present in the population under consideration.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Sangsari sheep · PCR-RFLP · FecB gene

Abstract

Phenotypic evaluation and the culling of candidate animals for traits by applying traditional animal breeding are usually costly tasks, which need to be carried out over a considerable span of time. The use of molecular genetics as an alternative method enables animal breeders to select eligible animals for the desirable trait, or traits, at earlier ages. Selection based upon markers could result in increased accuracy as well as a better selection response of animals. The Booroola gene has long been recognized as a candidate gene responsible for a higher rate of ewe ovulation, which results in increased litter size. In this study, blood samples were taken from 150 Sangsari sheep breed (140 ewes and 10 rams) in the Damghan animal breeding center using Venojects treated with an anticlot substance (EDTA). The sample DNA contents were salted out and extracted. After extraction, and after undertaking quantitative and qualitative tests (including spectrophotometry and gel agarose, 8%), the required amounts of DNA for polymerase chain reaction (PCR) were determined. Using the relevant primer, the related part was reproduced (190 bp) and then the PCR products were cut by AvaΠ enzymes for the gene, and 2 parts (30 bp and 160 bp) were produced for the target site. The results obtained in this study revealed that only the wild-type allele (+) was observed in the samples, indicating that, most likely, only genotype ++ was present in the population under consideration.

Özet

Phenotypic evaluation and the culling of candidate animals for traits by applying traditional animal breeding are usually costly tasks, which need to be carried out over a considerable span of time. The use of molecular genetics as an alternative method enables animal breeders to select eligible animals for the desirable trait, or traits, at earlier ages. Selection based upon markers could result in increased accuracy as well as a better selection response of animals. The Booroola gene has long been recognized as a candidate gene responsible for a higher rate of ewe ovulation, which results in increased litter size. In this study, blood samples were taken from 150 Sangsari sheep breed (140 ewes and 10 rams) in the Damghan animal breeding center using Venojects treated with an anticlot substance (EDTA). The sample DNA contents were salted out and extracted. After extraction, and after undertaking quantitative and qualitative tests (including spectrophotometry and gel agarose, 8%), the required amounts of DNA for polymerase chain reaction (PCR) were determined. Using the relevant primer, the related part was reproduced (190 bp) and then the PCR products were cut by AvaΠ enzymes for the gene, and 2 parts (30 bp and 160 bp) were produced for the target site. The results obtained in this study revealed that only the wild-type allele (+) was observed in the samples, indicating that, most likely, only genotype ++ was present in the population under consideration.

🔖

Cite This Article

JAMSHIDI, R., KASIRIAN, M. M., RAHIMI, G. A. (2013). Application of PCR-RFLP technique to determine Booroola gene polymorphism in the Sangsari sheep breed of Iran. Turkish Journal of Veterinary and Animal Sciences, Cilt: 37 - Sayı: 2, 129–133. https://ajindex.com/articles/121620

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (7)

  1. Davis, G.H., Balakrishnan, L., Ross, I.K., Wilson, T., Galloway, M., Lumsden, B.M., Hanrahan, J.P., Mullen, M.X., Mao, Z., Wang, G.L., Zhao, Z.S., Robinson, J.J., Mavrogenis, A.P., Papachristoforou, C., Peter, C., Baumung, R., Cardyn, P., Boujenane, I., Cockett, N.E., Eythorsdottir, E., Arranz, J.J., Notter, D.R.: Investigation of the Booroola (FecB) and Inverdale (FecXI) mutations in 21 prolific breeds and strains of sheep sampled in 13 countries. Anim. Reprod. Sci., 2006; 92: 87– Wilson, T., Wu, X.Y., Juengel, J.L., Ross, I.K., Lumsden, J.M., Lord, E.A., Dodds, K.G., Walling, G.A., McEwan, J.C., O’Connell, A.R., McNatty, K.P., Montgomery, G.W.: Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells. Biol. Reprod., 2001; 64: 1225–1235.
  2. Davis, GH., Galloway, S.M., Ross, I.K., Gergun, S.M., Ward J., Ghalsasi, P.M., Nimbker, C., Gray, G.D., Inounu, I., Tesnamurti, B., Hanrahan, J.P., Wilson, T.: DNA test in prolific sheep from eight countries provide new evidence on origin of the Booroola (FecB) mutation. Biology, 2002; 66: 1867–1879.
  3. Montgomery, G.W., Galloway, S.M., Davis, G.H., McNatty, K.P.: Genes controlling ovulation rate in sheep. Reproduction, 2001; 121: 843–852.
  4. McNatty, K.P., Jungel, J.L., Reader, K.L., Lun, S., Myllymaa, S., Lawrence, S.B., Western, A., Meerasahib, M.F., Mottershead, D.G., Groome, N.P., Ritvos, O., Laitinen, M.P.: Bone morphogenetic protein 15 and growth differentiation factor 9 co-operate to regulate granulose cell function in ruminants. Reproduction, 2005; 129: 481–487.
  5. Piper, L.R., Bindon, B.M.: The Booroola Merino and the performance of medium non-Peppin crosses at Armidale. In: Piper L.R., Bindon BM, Nethery R.D., Eds. The Booroola Merino. CSIRO, Melbourne. 1982; 9–19.
  6. Souza, C.J.H., MacDougall, C., Campbell, B.K., McNeilly, A.S., Baird, D.T.: The Booroola (FecB) phenotype is associated with a mutation in the bone morphogenetic receptor type 1B (BMPR1B) gene. J. Endocrinol., 2001; 169: R1–R6. Wang, G.L., Mao, X.Z., Davis, G.H., Zhao, Z.S., Zhang, L.J., Zeng, Y.Q.: DNA tests in Hu sheep and Han sheep (small tail) showed the existence of Booroola (FecB) mutation. J. Nanjing Agric. Univ., 2003; 26: 104–106.
  7. Mulsant, P., Lecerf, F., Fabre, S., Schibler, L., Monget, P., Lanneluc, I., Pisselet, C., Riquet, J., Monniaux, D., Callebaut, I., Cribiu, E., Thimonier, J., Teyssier, J., Bodin, L., Cognie, Y., C