Geographic Patterns of mtDNA Diversity in Europe

Genetic diversity in Europe has been interpreted as a reflection of phenomena occurring during the Paleolithic (∼45,000 years before the present [BP]), Mesolithic (∼18,000 years BP), and Neolithic (∼10,000 years BP) periods. A crucial role of the Neolithic demographic transition is supported by the...

Full description

Bibliographic Details
Main Authors: Simoni, Lucia, Calafell, Francesc, Pettener, Davide, Bertranpetit, Jaume, Barbujani, Guido
Format: Text
Language:English
Published: The American Society of Human Genetics 2000
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288355
http://www.ncbi.nlm.nih.gov/pubmed/10631156
id ftpubmed:oai:pubmedcentral.nih.gov:1288355
record_format openpolar
spelling ftpubmed:oai:pubmedcentral.nih.gov:1288355 2023-05-15T18:08:15+02:00 Geographic Patterns of mtDNA Diversity in Europe Simoni, Lucia Calafell, Francesc Pettener, Davide Bertranpetit, Jaume Barbujani, Guido 2000-01 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288355 http://www.ncbi.nlm.nih.gov/pubmed/10631156 en eng The American Society of Human Genetics http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288355 http://www.ncbi.nlm.nih.gov/pubmed/10631156 © 2000 by The American Society of Human Genetics. All rights reserved. Articles Text 2000 ftpubmed 2013-08-30T17:20:18Z Genetic diversity in Europe has been interpreted as a reflection of phenomena occurring during the Paleolithic (∼45,000 years before the present [BP]), Mesolithic (∼18,000 years BP), and Neolithic (∼10,000 years BP) periods. A crucial role of the Neolithic demographic transition is supported by the analysis of most nuclear loci, but the interpretation of mtDNA evidence is controversial. More than 2,600 sequences of the first hypervariable mitochondrial control region were analyzed for geographic patterns in samples from Europe, the Near East, and the Caucasus. Two autocorrelation statistics were used, one based on allele-frequency differences between samples and the other based on both sequence and frequency differences between alleles. In the global analysis, limited geographic patterning was observed, which could largely be attributed to a marked difference between the Saami and all other populations. The distribution of the zones of highest mitochondrial variation (genetic boundaries) confirmed that the Saami are sharply differentiated from an otherwise rather homogeneous set of European samples. However, an area of significant clinal variation was identified around the Mediterranean Sea (and not in the north), even though the differences between northern and southern populations were insignificant. Both a Paleolithic expansion and the Neolithic demic diffusion of farmers could have determined a longitudinal cline of mtDNA diversity. However, additional phenomena must be considered in both models, to account both for the north-south differences and for the greater geographic scope of clinal patterns at nuclear loci. Conversely, two predicted consequences of models of Mesolithic reexpansion from glacial refugia were not observed in the present study. Text saami PubMed Central (PMC)
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Articles
spellingShingle Articles
Simoni, Lucia
Calafell, Francesc
Pettener, Davide
Bertranpetit, Jaume
Barbujani, Guido
Geographic Patterns of mtDNA Diversity in Europe
topic_facet Articles
description Genetic diversity in Europe has been interpreted as a reflection of phenomena occurring during the Paleolithic (∼45,000 years before the present [BP]), Mesolithic (∼18,000 years BP), and Neolithic (∼10,000 years BP) periods. A crucial role of the Neolithic demographic transition is supported by the analysis of most nuclear loci, but the interpretation of mtDNA evidence is controversial. More than 2,600 sequences of the first hypervariable mitochondrial control region were analyzed for geographic patterns in samples from Europe, the Near East, and the Caucasus. Two autocorrelation statistics were used, one based on allele-frequency differences between samples and the other based on both sequence and frequency differences between alleles. In the global analysis, limited geographic patterning was observed, which could largely be attributed to a marked difference between the Saami and all other populations. The distribution of the zones of highest mitochondrial variation (genetic boundaries) confirmed that the Saami are sharply differentiated from an otherwise rather homogeneous set of European samples. However, an area of significant clinal variation was identified around the Mediterranean Sea (and not in the north), even though the differences between northern and southern populations were insignificant. Both a Paleolithic expansion and the Neolithic demic diffusion of farmers could have determined a longitudinal cline of mtDNA diversity. However, additional phenomena must be considered in both models, to account both for the north-south differences and for the greater geographic scope of clinal patterns at nuclear loci. Conversely, two predicted consequences of models of Mesolithic reexpansion from glacial refugia were not observed in the present study.
format Text
author Simoni, Lucia
Calafell, Francesc
Pettener, Davide
Bertranpetit, Jaume
Barbujani, Guido
author_facet Simoni, Lucia
Calafell, Francesc
Pettener, Davide
Bertranpetit, Jaume
Barbujani, Guido
author_sort Simoni, Lucia
title Geographic Patterns of mtDNA Diversity in Europe
title_short Geographic Patterns of mtDNA Diversity in Europe
title_full Geographic Patterns of mtDNA Diversity in Europe
title_fullStr Geographic Patterns of mtDNA Diversity in Europe
title_full_unstemmed Geographic Patterns of mtDNA Diversity in Europe
title_sort geographic patterns of mtdna diversity in europe
publisher The American Society of Human Genetics
publishDate 2000
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288355
http://www.ncbi.nlm.nih.gov/pubmed/10631156
genre saami
genre_facet saami
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288355
http://www.ncbi.nlm.nih.gov/pubmed/10631156
op_rights © 2000 by The American Society of Human Genetics. All rights reserved.
_version_ 1766180519196753920