Traces of forgotten historical events in mountain communities in Central Italy: A genetic insight

Am J Hum Biol. 2015 Jul-Aug;27(4):508-19. doi: 10.1002/ajhb.22677. Epub 2015 Feb 27.

Abstract

Objectives: Analysis of human genetic variation in mountain communities can shed light on the peopling of mountainous regions, perhaps revealing whether the remote geographic location spared them from outside invasion and preserved their gene pool from admixture. In this study, we created a model to assess genetic traces of historical events by reconstructing the paternal and maternal genetic history of seven small mountain villages in inland valleys of Central Italy.

Methods: The communities were selected for their geographic isolation, attested biodemographic stability, and documented history prior to the Roman conquest. We studied the genetic structure by analyzing two hypervariable segments (HVS-I and HVS-II) of the mtDNA D-loop and several informative single nucleotide polymorphisms (SNPs) of the mtDNA coding region in 346 individuals, in addition to 17 short tandem repeats (STRs) and Y-chromosome SNPs in 237 male individuals.

Results: For both uniparental markers, most of the haplogroups originated in Western Europe while some Near Eastern haplogroups were identified at low frequencies. However, there was an evident genetic similarity between the Central Italian samples and Near Eastern populations mainly in the male genetic pool.

Conclusions: The samples highlight an overall European genetic pattern both for mtDNA and Y chromosome. Notwithstanding this scenario, Y chromosome haplogroup Q, a common paternal lineage in Central/Western Asia but almost Europe-wide absent, was found, suggesting that Central Italy could have hosted a settlement from Anatolia that might be supported by cultural, topographic and genetic evidence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asia, Western
  • Chromosomes, Human, Y / genetics*
  • DNA, Mitochondrial / genetics*
  • Europe
  • Female
  • Genetic Variation*
  • Humans
  • Italy
  • Male
  • Microsatellite Repeats*
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Young Adult

Substances

  • DNA, Mitochondrial