Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed

The BMPR-1B/FecBor Booroolagene is the first major fecundity gene identified in sheep. The present investigation was carried out to study polymorphism by PCR-RFLP of FecB gene in 30 ewes belonging to the Northeast Bulgarian Merino sheep breed. Genomic DNA was extracted from whole bloo...

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Main Authors: Milena Bozhilova-Sakova, Ivona Dimitrova, Maya Ignatova
Format: Article
Language:English
Published: Plovdiv University Press 2020-12-01
Series:Journal of BioScience and Biotechnology
Subjects:
Online Access:https://editorial.uni-plovdiv.bg/index.php/JBB/article/view/328/258
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spelling doaj-3f42fa4ea311470fa3d6eb857919af272020-12-25T08:38:19ZengPlovdiv University Press Journal of BioScience and Biotechnology1314-62381314-62462020-12-01921922Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed Milena Bozhilova-Sakova0Ivona Dimitrova1Maya Ignatova2Institute of Animal Science – Kostinbrod2232 Kostinbrod, Bulgaria.University of Forestry, Faculty of Agronomy 10, Kl. Ohridski bl., 1756 Sofia, BulgariaInstitute of Animal Science – Kostinbrod2232 Kostinbrod, Bulgaria.The BMPR-1B/FecBor Booroolagene is the first major fecundity gene identified in sheep. The present investigation was carried out to study polymorphism by PCR-RFLP of FecB gene in 30 ewes belonging to the Northeast Bulgarian Merino sheep breed. Genomic DNA was extracted from whole blood. PCR amplification of FecBgene revealed fragments with length 190 bp using a specific primer set. After PCR-RFLP analysis it was found the wild allele “+” and the mutant allele “B” with frequencies 0.97 and 0.03, respectively.This is the first studyin Bulgarian sheep breeds, where wasfoundthe presence of Booroola mutation. According to the results the genotype frequencies were as followed: wild homozygous genotype “++” 0.93 and heterozygous genotype “B+” 0.07, respectively. The observed (Ho) and expected heterozygosity (He) were 0.066 and 0.058, respectively. It can be concluded that the studied herd was in Hardy-Weinberg equilibrium. PCR-RFLP technique can be used to detect and genotype the FecBgene clearly.https://editorial.uni-plovdiv.bg/index.php/JBB/article/view/328/258sheepnortheast bulgarian merino breedbmpr-1b/fecb genepcr-rflp analysis
collection DOAJ
language English
format Article
sources DOAJ
author Milena Bozhilova-Sakova
Ivona Dimitrova
Maya Ignatova
spellingShingle Milena Bozhilova-Sakova
Ivona Dimitrova
Maya Ignatova
Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
Journal of BioScience and Biotechnology
sheep
northeast bulgarian merino breed
bmpr-1b/fecb gene
pcr-rflp analysis
author_facet Milena Bozhilova-Sakova
Ivona Dimitrova
Maya Ignatova
author_sort Milena Bozhilova-Sakova
title Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
title_short Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
title_full Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
title_fullStr Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
title_full_unstemmed Genetic diversity of Booroola gene in Northeast Bulgarian Merino sheep breed
title_sort genetic diversity of booroola gene in northeast bulgarian merino sheep breed
publisher Plovdiv University Press
series Journal of BioScience and Biotechnology
issn 1314-6238
1314-6246
publishDate 2020-12-01
description The BMPR-1B/FecBor Booroolagene is the first major fecundity gene identified in sheep. The present investigation was carried out to study polymorphism by PCR-RFLP of FecB gene in 30 ewes belonging to the Northeast Bulgarian Merino sheep breed. Genomic DNA was extracted from whole blood. PCR amplification of FecBgene revealed fragments with length 190 bp using a specific primer set. After PCR-RFLP analysis it was found the wild allele “+” and the mutant allele “B” with frequencies 0.97 and 0.03, respectively.This is the first studyin Bulgarian sheep breeds, where wasfoundthe presence of Booroola mutation. According to the results the genotype frequencies were as followed: wild homozygous genotype “++” 0.93 and heterozygous genotype “B+” 0.07, respectively. The observed (Ho) and expected heterozygosity (He) were 0.066 and 0.058, respectively. It can be concluded that the studied herd was in Hardy-Weinberg equilibrium. PCR-RFLP technique can be used to detect and genotype the FecBgene clearly.
topic sheep
northeast bulgarian merino breed
bmpr-1b/fecb gene
pcr-rflp analysis
url https://editorial.uni-plovdiv.bg/index.php/JBB/article/view/328/258
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