HVS-I polymorphism screening of ancient human mitochondrial DNA provides evidence for N9a discontinuity and East Asian haplogroups in the Neolithic Hungary

Zsuzsanna Guba, Éva Hadadi, Ágnes Major, Tünde Furka, Emese Juhász, Judit Koós, Károly Nagy, Tamás Zeke

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Analysis of mitochondrial mutations in the HVS-I region is an effective method for ancient human populational studies. Discontinuous haplotype data between the first farmers and contemporary Europeans has been described before. Our contribution is based on a survey initiated on the Neolithic skeletons from Hungarian archaeological sites in the Alföld. This Lowland, the Hungarian Plain, is well excavated as an important region for spread of Neolithic culture from Near East and Balkans toward Central and Western Europe, started circa 8000 years ago. HVS-I sequences from nt15977 to nt16430 of 11 such specimens with sufficient mitochondrial DNA preservation among an extended Neolithic collection were analysed for polymorphisms, identifying 23 different ones. After assigning all single-nucleotide polymorphisms, a novel, N9a, N1a, C5, D1/G1a, M/R24 haplogroups were determined. On mitochondrial control mutations at nt16257 and nt16261, polymorphic PCRs were carried out to assess their distribution in remains. Neolithic data set was compared with contemporary Vác samples and references, resulting in higher frequency of N9a in Alföld as a remarkable genetic discontinuity. Our investigation is the first to study mutations form Neolithic of Hungary, resulting in an outcome of Far Eastern haplogroups in the Carpathian Basin. It is worth further investigation as a non-descendant theory, instead of a continuous population history, supporting genetic gaps between ancient and recent human populations.

Original languageEnglish
Pages (from-to)784-796
Number of pages13
JournalJournal of Human Genetics
Volume56
Issue number11
DOIs
Publication statusPublished - Nov 1 2011

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Keywords

  • N9a haplogroup
  • ancient DNA
  • mitochondrial control mutation
  • neolithisation
  • polymorphic PCR

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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