Factor V Leiden in an Urartian, Dating Back to 1000 BC

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Alakoc Y., Aka P. S., Egin Y., Akar N.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, cilt.16, sa.6, ss.679-683, 2010 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 16 Sayı: 6
  • Basım Tarihi: 2010
  • Doi Numarası: 10.1177/1076029609338045
  • Dergi Adı: CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.679-683
  • Anahtar Kelimeler: factor V Leiden, Urartian, ancient DNA, selective advantage, orthograte entrance technique, ACTIVATED PROTEIN-C, TURKISH POPULATION, GENE POLYMORPHISMS, MUTATION, DNA, PREVALENCE, REMAINS, SINGLE, CONTAMINATION, RESISTANCE
  • Ankara Üniversitesi Adresli: Evet

Özet

Factor V Leiden (FVL) is the most common monogenic disorder that causes activated protein C (APC) resistance, creating hyper-coagulation. The mutation shows an uneven geographic distribution, significantly high in European populations. The mutation is believed to have originated approximately 20 000 years ago probably from a geographic region close to Anatolia. This fact makes it noteworthy to search for the mutation in ancient populations that once lived in this area. One of these civilizations, Urartu was centered around Van Lake in Eastern Turkey. The archeological remains from the excavations of the region are dated back to 1000 BC. Teeth, taken from the excavations of Van Yoncatepe fortress, were taken into DNA analysis considering all the precautions for ancient DNA analysis. Multiplex STR (Short Tandem Repeats) analysis were performed both to determine the gender of the samples and to conclude that the samples are preserved from modern DNA contamination. After getting an 80% amplification success for amelogenin, a melting curve analysis using lightcycler was performed to determine the FVL genotype of each sample. Of the 60 samples, 1 gave a positive amplification result for FV gene and was found to be heterozygous. To date, the age of this mutation was estimated based on statistical calculations using haplotype frequencies; here for the first time, we report FVL in an ancient population of 3000 years.