ArticleBMC evolutionary biology2008
Timing and deciphering mitochondrial DNA macro-haplogroup R0 variability in Central Europe and Middle East.
Article in BMC evolutionary biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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21 citing papers in PubMed.
- Intensive post-war migrations and mtDNA variation based on Poland case.Scientific reports · 2025Article
- Persistence of Ancestral KhoeSan Mitochondrial Patterns in Contemporary South African Populations.Annals of human genetics · 2025Article
- Deciphering the maternal ancestral lineage of Greek Cypriots, Armenian Cypriots and Maronite Cypriots.PloS one · 2024Article
- Genomes from a medieval mass burial show Ashkenazi-associated hereditary diseases pre-date the 12th century.Current biology : CB · 2022Article
- Ancient Human Migrations to and through Jammu Kashmir- India were not of Males Exclusively.Scientific reports · 2018Article
- The distribution of mitochondrial DNA haplogroup H in southern Iberia indicates ancient human genetic exchanges along the western edge of the Mediterranean.BMC genetics · 2017Article
- Genetic affinities among the historical provinces of Romania and Central Europe as revealed by an mtDNA analysis.BMC genetics · 2017Article
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- Mitogenomes from The 1000 Genome Project reveal new Near Eastern features in present-day Tuscans.PloS one · 2015Article
- Uniparental markers in Italy reveal a sex-biased genetic structure and different historical strata.PloS one · 2013Article
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- Bulgarians vs the other European populations: a mitochondrial DNA perspective.International journal of legal medicine · 2012Article
- Mitochondrial haplogroups and control region polymorphisms in age-related macular degeneration: a case-control study.PloS one · 2012Article
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- Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease.PloS one · 2010Article
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- The maternal aborigine colonization of La Palma (Canary Islands).European journal of human genetics : EJHG · 2009Article
- Linguistic and maternal genetic diversity are not correlated in Native Mexicans.Human genetics · 2009Article
- Sequencing strategy for the whole mitochondrial genome resulting in high quality sequences.BMC genomics · 2009Article
- Mitochondrial DNA haplogroup H structure in North Africa.BMC genetics · 2009Article
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8 authors.
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Abstract
backgroundNearly half of the West Eurasian assemblage of human mitochondrial DNA (mtDNA) is fractioned into numerous sub-lineages of the predominant haplogroup (hg) R0. Several hypotheses have been proposed on the origin and the expansion times of some R0 sub-lineages, which were partially inconsistent with each other. Here we describe the phylogenetic structure and genetic variety of hg R0 in five European populations and one population from the Middle East.
resultsOur analysis of 1,350 mtDNA haplotypes belonging to R0, including entire control region sequences and 45 single nucleotide polymorphisms from the coding region, revealed significant differences in the distribution of different sub-hgs even between geographically closely located regions. Estimates of coalescence times that were derived using diverse algorithmic approaches consistently affirmed that the major expansions of the different R0 hgs occurred in the terminal Pleistocene and early Holocene.
conclusionGiven an estimated coalescence time of the distinct lineages of 10-18 kya, the differences in the distributions could hint to either limited maternal gene flow after the Last Glacial Maximum due to the alpine nature of the regions involved or to a stochastic loss of diversity due to environmental events and/or disease episodes occurred at different times and in distinctive regions. Our comparison of two different ways of obtaining the timing of the most recent common ancestor confirms that the time of a sudden expansion can be adequately recovered from control region data with valid confidence intervals. For reliable estimates, both procedures should be applied in order to cross-check the results for validity and soundness.
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