Evidence map›Paper›PMID 30467412›Full record

ArticleEuropean journal of human genetics : EJHG2019

The role of matrilineality in shaping patterns of Y chromosome and mtDNA sequence variation in southwestern Angola.

Sandra Oliveira, Alexander Hübner, Anne-Maria Fehn, Teresa Aço, Fernanda Lages, Brigitte Pakendorf, Mark Stoneking, Jorge Rocha

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. The paternal and maternal genetic history of Vietnamese populations.European journal of human genetics : EJHG · 2020
    Article
  7. Review
  8. Article
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

8 authors.

Sandra OliveiraCIBIO/InBIO: Research Center in Biodiversity and Genetic Resources, 4485-661, Vairão, Portugal. sroliveiraa@gmail.com.
Alexander HübnerDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103, Leipzig, Germany.ORCID http://orcid.org/0000-0003-3572-9996
Anne-Maria FehnCIBIO/InBIO: Research Center in Biodiversity and Genetic Resources, 4485-661, Vairão, Portugal.
Teresa AçoCentro de Estudos do Deserto (CEDO), Namibe, Angola.
Fernanda LagesISCED/Huíla-Instituto Superior de Ciências da Educação, Lubango, Angola.
Brigitte PakendorfLaboratoire Dynamique du Langage, UMR5596, CNRS & Univ Lyon, 69007, Lyon, France.
Mark StonekingDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103, Leipzig, Germany.
Jorge RochaCIBIO/InBIO: Research Center in Biodiversity and Genetic Resources, 4485-661, Vairão, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Southwestern Angola is a region characterized by contact between indigenous foragers and incoming food-producers, involving genetic and cultural exchanges between peoples speaking Kx'a, Khoe-Kwadi, and Bantu languages. Although present-day Bantu speakers share a patrilocal residence pattern and matrilineal principle of clan and group membership, a highly stratified social setting divides dominant pastoralists from marginalized groups that subsist on alternative strategies and have previously been thought to have pre-Bantu origins. Here, we compare new high-resolution sequence data from 2.3 Mb of the male-specific region of the Y chromosome (MSY) from 170 individuals with previously reported mitochondrial DNA (mtDNA) genomes, to investigate the population history of seven representative southwestern Angolan groups (Himba, Kuvale, Kwisi, Kwepe, Twa, Tjimba, !Xun), and to study the causes and consequences of sex-biased processes in their genetic variation. We found no clear link between the formerly Kwadi-speaking Kwepe and pre-Bantu eastern African migrants, and no pre-Bantu MSY lineages among Bantu-speaking groups, except for small amounts of "Khoisan" introgression. We therefore propose that irrespective of their subsistence strategies, all Bantu-speaking groups of the area share a male Bantu origin. Additionally, we show that in Bantu-speaking groups, the levels of among-group and between-group variation are higher for mtDNA than for MSY. These results, together with our previous demonstration that the matriclanic systems of southwestern Angolan Bantu groups are genealogically consistent, suggest that matrilineality strongly enhances both female population sizes and interpopulation mtDNA variation.

Indexed as

Polymorphism, GeneticAngolaChromosomes, Human, YDNA, MitochondrialFemaleHumansMalePopulationDNA, Mitochondrial

Identifiers

PMID30467412
PMCPMC6460574

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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.