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Identification of factor XI deficiency in Holstein cattle in Turkey

Authors
  • Meydan, Hasan1
  • Yildiz, Mehmet A1
  • Özdil, Fulya2
  • Gedik, Yasemin1
  • Özbeyaz, Ceyhan3
  • 1 Animal Sciences, Ankara University, Faculty of Agriculture, Ankara, 06110, Turkey , Ankara
  • 2 Animal Sciences, Selçuk University, Faculty of Agriculture, Konya, 42075, Turkey , Konya
  • 3 Ankara University, Faculty of Veterinary Medicine, Ankara, 06110, Turkey , Ankara
Type
Published Article
Journal
Acta Veterinaria Scandinavica
Publisher
BioMed Central
Publication Date
Jan 22, 2009
Volume
51
Issue
1
Identifiers
DOI: 10.1186/1751-0147-51-5
Source
Springer Nature
Keywords
License
Green

Abstract

BackgroundFactor XI (FXI) is a plasma protein that participates in the formation of blood clots. Factor XI deficiency is autosomal recessive hereditary disorder that may be associated with excess bleeding in Holstein cattle.MethodsIn this study, 225 Holstein cows reared in Turkey were screened in order to identify FXI genotypes. DNA extractions were obtained from the fresh blood of the cows. Amplicons of FXI exon 12 were obtained by Polymerase Chain Reaction (PCR), and analyzed by 2% agarose gel electrophoresis stained with ethidium bromide. Additionally, all cows were confirmed by DNA sequencing to determine whether or not there was a mutant allele.ResultsCarriers of the FXI deficiency have two DNA fragments of 320 bp and 244 bp in size. The results of our study demonstrated that only four out of the 225 Holstein cows tested in Turkey carried the FXI deficiency. The frequency of the mutant FXI allele and the prevalence of heterozygous cows were found as 0.9% and 1.8%, respectively.ConclusionThe DNA-based test determines all genotypes, regardless of phenotype or FXI activity. The mutation responsible for the FXI deficiency had not been detected in Holstein cattle in Turkey before prior to this study. The frequency of the mutant FXI allele needs to be confirmed by carrying out further analyses on cattle in Turkey and the selection programs should be developed to eliminate this genetic disorder.

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