Evidence map›Paper›PMID 27904152›Full record

ArticleJournal of human genetics2017

Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania.

Nano Nagle, Kaye N Ballantyne, Mannis van Oven, Chris Tyler-Smith, Yali Xue, Stephen Wilcox, Leah Wilcox, Rust Turkalov, Roland A H van Oorschot, Sheila van Holst Pellekaan and 6 more

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In one paragraph

Article in Journal of human genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

16 authors.

Nano NagleDepartment of Biochemistry and Genetics, La Trobe University, Melbourne, VIC, Australia.
Kaye N BallantyneOffice of the Chief Forensic Scientist, Victorian Police Forensic Services Department, Melbourne, VIC, Australia.
Mannis van OvenDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
Chris Tyler-SmithThe Wellcome Trust Sanger Institute, Welcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.
Yali XueThe Wellcome Trust Sanger Institute, Welcome Trust Genome Campus, Hinxton, Cambridgeshire, UK.
Stephen WilcoxAustralian Genome Research Facility, Melbourne, VIC, Australia.
Leah WilcoxDepartment of Biochemistry and Genetics, La Trobe University, Melbourne, VIC, Australia.
Rust TurkalovAustralian Genome Research Facility, Melbourne, VIC, Australia.
Roland A H van OorschotOffice of the Chief Forensic Scientist, Victorian Police Forensic Services Department, Melbourne, VIC, Australia.
Sheila van Holst PellekaanSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW, Australia.
Theodore G SchurrDepartment of Anthropology, University of Pennsylvania, Philadelphia, PA, USA.
Peter McAllisterGriffith University, Nathan, QLD, Australia.
Lesley WilliamsCommunity Elder and Cultural Advisor, Brisbane, QLD, Australia.
Manfred KayserDepartment of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
R John MitchellDepartment of Biochemistry and Genetics, La Trobe University, Melbourne, VIC, Australia.
Genographic Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aboriginal Australians are one of the more poorly studied populations from the standpoint of human evolution and genetic diversity. Thus, to investigate their genetic diversity, the possible date of their ancestors' arrival and their relationships with neighboring populations, we analyzed mitochondrial DNA (mtDNA) diversity in a large sample of Aboriginal Australians. Selected mtDNA single-nucleotide polymorphisms and the hypervariable segment haplotypes were analyzed in 594 Aboriginal Australians drawn from locations across the continent, chiefly from regions not previously sampled. Most (~78%) samples could be assigned to mtDNA haplogroups indigenous to Australia. The indigenous haplogroups were all ancient (with estimated ages >40 000 years) and geographically widespread across the continent. The most common haplogroup was P (44%) followed by S (23%) and M42a (9%). There was some geographic structure at the haplotype level. The estimated ages of the indigenous haplogroups range from 39 000 to 55 000 years, dates that fit well with the estimated date of colonization of Australia based on archeological evidence (~47 000 years ago). The distribution of mtDNA haplogroups in Australia and New Guinea supports the hypothesis that the ancestors of Aboriginal Australians entered Sahul through at least two entry points. The mtDNA data give no support to the hypothesis of secondary gene flow into Australia during the Holocene, but instead suggest long-term isolation of the continent.

Indexed as

Genetic VariationPhylogenyBiological EvolutionDNA, MitochondrialFemaleGene FlowHaplotypesHistory, 21st CenturyHistory, AncientHumansMaleOceaniaPaleontologyPhylogeographyPolymorphism, Single NucleotideReproductive IsolationDNA, Mitochondrial

Identifiers

PMID27904152

What OpenQuestion holds

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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.