Evidence map›Paper›PMID 8940282›Full record

ArticleAmerican journal of human genetics1996

High mitochondrial sequence diversity in linguistic isolates of the Alps.

M Stenico, L Nigro, G Bertorelle, F Calafell, M Capitanio, C Corrain, G Barbujani

Abstract read
In one paragraph

Article in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Etruscan artifacts.American journal of human genetics · 2004
    Article
  6. The fingerprint of phantom mutations in mitochondrial DNA data.American journal of human genetics · 2002
    Article
  7. Article
  8. Geographic patterns of mtDNA diversity in Europe.American journal of human genetics · 2000
    Article
  9. Why hunter-gatherer populations do not show signs of pleistocene demographic expansions.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  10. Using rare mutations to estimate population divergence times: a maximum likelihood approach.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. DNA variation and language affinities.American journal of human genetics · 1997
    Article
  16. An apportionment of human DNA diversity.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

M StenicoDipartimento di Biologia, Universita di Padova, Italy.
L Nigro
G Bertorelle
F Calafell
M Capitanio
C Corrain
G Barbujani

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Segment I of the control region of mtDNA (360 bases) was sequenced in seven samples, each of 10 individuals inhabiting villages in the eastern Italian Alps (South Tyrol and Trentino). Three linguistic groups, German, Italian, and Ladin, were represented by two samples each; the seventh sample comes from an isolated group of German origin, the Mocheni, who are linguistically distinct and geographically separated from the bulk of the German speakers. Seventy-four polymorphic sites were identified, defining 63 different haplotypes. Mocheni and Ladin speakers tend to form two clusters in the evolutionary trees inferred from sequences. Analysis of molecular variance shows significant differentiation within samples, among them, and among linguistic groups. Genetic differences between the Ladins and the other groups are not much smaller than between Europeans and some Africans; variation is large within groups, as well, with the exception of only the Mocheni. In the evolutionary trees where the four alpine groups are compared with other European populations, Mocheni and especially Ladins appear as clear outliers. Romansch-speaking Swiss, who are linguistically related to Ladins, are not genetically similar to them, for this segment of DNA. Because the time elapsed since colonization of the Alps (< or = 12,000 years) is short in mutational terms, the only model accounting for the observed relationships between mtDNA variation and linguistic identity seems one in which a population ancestral to Ladin speakers was already differentiated long before the Alps were settled and the current linguistic affiliations were established. For the Mocheni, the results are consistent with a simpler episode of allele loss, from an original genetic pool common to the ancestors of the current German speakers.

Indexed as

LinguisticsModels, GeneticDNA, MitochondrialEuropeFounder EffectGene FrequencyGenetic VariationHaplotypesHumansItalyPhylogenySequence Analysis, DNADNA, Mitochondrial

Identifiers

PMID8940282
PMCPMC1914857

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.