Investigation of FecB Mutation in Four Romanian Sheep Breeds
Hyperprolific phenotype of Booroola sheep was first discovered in the Australian Merino breed. This phenotype is due to the action of a single autosomal gene that influences the number of ovulations per estrogenic cycle. Recent discoveries have revealed that high prolificacy in Booroola Merino sheep...
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Agroprint Timisoara
2011-05-01
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doaj-24b7b3c181e54230b0f4414a70b953c82020-11-25T03:41:22ZengAgroprint TimisoaraScientific Papers Animal Science and Biotechnologies1841-93642344-45762011-05-01441219222398Investigation of FecB Mutation in Four Romanian Sheep BreedsSergiu-Emil Georgescu0Gheorghe Hrinca1Mariana Rebedea2Marieta Costache3University of Bucharest, Faculty of Biology, Department of Biochemistry and Molecular Biology, BucharestPopauti Research and Development Station for Sheeps and Goats Growth, RachitiUniversity of Bucharest, Faculty of Biology, Department of Biochemistry and Molecular Biology, BucharestUniversity of Bucharest, Faculty of Biology, Department of Biochemistry and Molecular Biology, BucharestHyperprolific phenotype of Booroola sheep was first discovered in the Australian Merino breed. This phenotype is due to the action of a single autosomal gene that influences the number of ovulations per estrogenic cycle. Recent discoveries have revealed that high prolificacy in Booroola Merino sheep is the result of a mutation (FecB) in the bone morphogenetic protein receptor 1B (BMPR-1B) gene. This mutation is located in the highly conserved kinase domain of the bone morphogenetic protein receptor IB, and is characterized by precocious differentiation of ovarian follicles, leading to the production of large numbers of ovulatory follicles. Our objective was to develop an easy method to identify the FecB mutation in order to screen sheep populations in terms of prolificacy. We designed primers to amplify a 190 bp fragment from the BMPR-1B gene containing or lacking the mutation. The PCR product was cut with AvaII endonuclease and the restriction products were analysed by agarose gel electrophoresis. Using the PCR-RFLP technique, we established an easy and efficient method that can be used to screen the FecB mutation. Therefore, these new methods increase the panel of molecular tools available for sheep breeders to choose the most prolific genotypes for improving artificial selection.http://spasb.ro/index.php/spasb/article/view/474fecbpcr-rflpprolificacyscreeningsheep |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sergiu-Emil Georgescu Gheorghe Hrinca Mariana Rebedea Marieta Costache |
spellingShingle |
Sergiu-Emil Georgescu Gheorghe Hrinca Mariana Rebedea Marieta Costache Investigation of FecB Mutation in Four Romanian Sheep Breeds Scientific Papers Animal Science and Biotechnologies fecb pcr-rflp prolificacy screening sheep |
author_facet |
Sergiu-Emil Georgescu Gheorghe Hrinca Mariana Rebedea Marieta Costache |
author_sort |
Sergiu-Emil Georgescu |
title |
Investigation of FecB Mutation in Four Romanian Sheep Breeds |
title_short |
Investigation of FecB Mutation in Four Romanian Sheep Breeds |
title_full |
Investigation of FecB Mutation in Four Romanian Sheep Breeds |
title_fullStr |
Investigation of FecB Mutation in Four Romanian Sheep Breeds |
title_full_unstemmed |
Investigation of FecB Mutation in Four Romanian Sheep Breeds |
title_sort |
investigation of fecb mutation in four romanian sheep breeds |
publisher |
Agroprint Timisoara |
series |
Scientific Papers Animal Science and Biotechnologies |
issn |
1841-9364 2344-4576 |
publishDate |
2011-05-01 |
description |
Hyperprolific phenotype of Booroola sheep was first discovered in the Australian Merino breed. This phenotype is due to the action of a single autosomal gene that influences the number of ovulations per estrogenic cycle. Recent discoveries have revealed that high prolificacy in Booroola Merino sheep is the result of a mutation (FecB) in the bone morphogenetic protein receptor 1B (BMPR-1B) gene. This mutation is located in the highly conserved kinase domain of the bone morphogenetic protein receptor IB, and is characterized by precocious differentiation of ovarian follicles, leading to the production of large numbers of ovulatory follicles. Our objective was to develop an easy method to identify the FecB mutation in order to screen sheep populations in terms of prolificacy. We designed primers to amplify a 190 bp fragment from the BMPR-1B gene containing or lacking the mutation. The PCR product was cut with AvaII endonuclease and the restriction products were analysed by agarose gel electrophoresis. Using the PCR-RFLP technique, we established an easy and efficient method that can be used to screen the FecB mutation. Therefore, these new methods increase the panel of molecular tools available for sheep breeders to choose the most prolific genotypes for improving artificial selection. |
topic |
fecb pcr-rflp prolificacy screening sheep |
url |
http://spasb.ro/index.php/spasb/article/view/474 |
work_keys_str_mv |
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