Evidence map›Paper›PMID 19221006›Full record

ArticleMolecular biology and evolution2009

Haplotypic background of a private allele at high frequency in the Americas.

Kari B Schroeder, Mattias Jakobsson, Michael H Crawford, Theodore G Schurr, Simina M Boca, Donald F Conrad, Raul Y Tito, Ludmilla P Osipova, Larissa A Tarskaia, Sergey I Zhadanov and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

19 citing papers in PubMed, 89 citations in OpenAlex.

  1. On the heterozygosity of an admixed population.Journal of mathematical biology · 2020
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  4. A genomic view of the peopling of the Americas.Current opinion in genetics & development · 2016
    Review
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  9. Reconciling migration models to the Americas with the variation of North American native mitogenomes.Proceedings of the National Academy of Sciences of the United States of America · 2013
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 12 institutions in 6 countries.

Kari B SchroederDepartment of Anthropology, University of California, Davis, CA, USA. kbschroeder@ucdavis.edu
Mattias Jakobsson
Michael H Crawford
Theodore G Schurr
Simina M Boca
Donald F Conrad
Raul Y Tito
Ludmilla P Osipova
Larissa A Tarskaia
Sergey I Zhadanov
Jeffrey D Wall
Jonathan K Pritchard
Ripan S Malhi
David G Smith
Noah A Rosenberg
University of California, San Francisco · USUniversity of Chicago · USUniversity of Illinois Urbana-Champaign · USCalifornia University of Pennsylvania · USCzech Academy of Sciences, Institute of Molecular Genetics · CZInstitute of Cytology and Genetics · RUJohns Hopkins University · USUniversity of California, Davis · USUniversity of California System · USUniversity of Kansas · USUniversity of Michigan · USUppsala University · SE

Funding

GENETIC MANAGEMENT OF MECAQUES BY DNA RFLP ANALYSISR24RR005090 · NCRR · UNIVERSITY OF CALIFORNIA DAVIS · PI SMITH, DAVID GLENN · 1988 to 2011
$3.7M
Population-Genetic Studies for Association MappingR01GM081441 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSENBERG, NOAH · 2007 to 2011
$1.7M
NCRR NIH HHS R24 RR005090NCRR NIH HHS R24RR005090NIGMS NIH HHS R01 GM081441
6 · The paper itself

Abstract

Recently, the observation of a high-frequency private allele, the 9-repeat allele at microsatellite D9S1120, in all sampled Native American and Western Beringian populations has been interpreted as evidence that all modern Native Americans descend primarily from a single founding population. However, this inference assumed that all copies of the 9-repeat allele were identical by descent and that the geographic distribution of this allele had not been influenced by natural selection. To investigate whether these assumptions are satisfied, we genotyped 34 single nucleotide polymorphisms across approximately 500 kilobases (kb) around D9S1120 in 21 Native American and Western Beringian populations and 54 other worldwide populations. All chromosomes with the 9-repeat allele share the same haplotypic background in the vicinity of D9S1120, suggesting that all sampled copies of the 9-repeat allele are identical by descent. Ninety-one percent of these chromosomes share the same 76.26 kb haplotype, which we call the "American Modal Haplotype" (AMH). Three observations lead us to conclude that the high frequency and widespread distribution of the 9-repeat allele are unlikely to be the result of positive selection: 1) aside from its association with the 9-repeat allele, the AMH does not have a high frequency in the Americas, 2) the AMH is not unusually long for its frequency compared with other haplotypes in the Americas, and 3) in Latin American mestizo populations, the proportion of Native American ancestry at D9S1120 is not unusual compared with that observed at other genomewide microsatellites. Using a new method for estimating the time to the most recent common ancestor (MRCA) of all sampled copies of an allele on the basis of an estimate of the length of the genealogy descended from the MRCA, we calculate the mean time to the MRCA of the 9-repeat allele to be between 7,325 and 39,900 years, depending on the demographic model used. The results support the hypothesis that all modern Native Americans and Western Beringians trace a large portion of their ancestry to a single founding population that may have been isolated from other Asian populations prior to expanding into the Americas.

Indexed as

Gene FrequencyHaplotypesAgingAllelesAmerican Indian or Alaska NativeAmericasAsian PeopleChromosomes, Human, Pair 9DemographyGenealogy and HeraldryGenetics, PopulationHumansModels, GeneticPolymorphism, Single NucleotideRecombination, GeneticSelection, Genetic

Identifiers

PMID19221006
PMCPMC2734135
OpenAlexW2138758320

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.