Evidence map›Paper›PMID 42236926›Full record

ArticleCommunications biology2026

Revisiting the African mtDNA landscape through complete mitochondrial genomes.

Imke Lankheet, Afifa Chowdhury, Christian Tellgren-Roth, Cécile Jolly, André E R Soares, Miguel de Navascués, Sara Pacchiarotti, Lorenzo Maselli, Guy Kouarata, Jean-Pierre Donzo and 19 more

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

29 authors.

Imke LankheetHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-4434-1934
Afifa ChowdhuryHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID 0009-0000-8509-0276
Christian Tellgren-RothDepartment of Immunology, Genetics and Pathology, Uppsala Genome Center, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-0502-3693
Cécile JollyHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden.
André E R SoaresDepartment of Medical Biochemistry and Microbiology, Uppsala University, National Bioinformatics Infrastructure Sweden, Uppsala, Sweden.ORCID 0000-0002-7768-2199
Miguel de NavascuésCBGP, INRAE, CIRAD, IRD, Institute Agro, University of Montpellier, Montpellier, France.ORCID 0000-0001-8342-6047
Sara PacchiarottiUGent Centre for Bantu Studies (BantUGent), Department of Languages and Cultures, Ghent University, Ghent, Belgium.ORCID 0000-0003-1360-5060
Lorenzo MaselliUGent Centre for Bantu Studies (BantUGent), Department of Languages and Cultures, Ghent University, Ghent, Belgium.ORCID 0000-0002-1707-1054
Guy KouarataUGent Centre for Bantu Studies (BantUGent), Department of Languages and Cultures, Ghent University, Ghent, Belgium.
Jean-Pierre DonzoUGent Centre for Bantu Studies (BantUGent), Department of Languages and Cultures, Ghent University, Ghent, Belgium.
Vinet CoetzeeDepartment of Biochemistry, Genetics and Microbiology, University of Pretoria, Pretoria, South Africa.
Minique de CastroBiotechnology Platform, Agricultural Research Council, Onderstepoort, Pretoria, South Africa.
Peter EbbesenDepartment of Health Science and Technology, University of Aalborg, Aalborg, Denmark.
Edita PriehodováArchaeogenetics Laboratory, Institute of Archaeology of the Czech Academy of Sciences, Prague, Czech Republic.
Eliška PodgornáArchaeogenetics Laboratory, Institute of Archaeology of the Czech Academy of Sciences, Prague, Czech Republic.
Viktor ČernýArchaeogenetics Laboratory, Institute of Archaeology of the Czech Academy of Sciences, Prague, Czech Republic.
Susanne T GreenSchool of Geography, Archaeology and Environmental Studies, University of the Witwatersrand, Johannesburg, South Africa.
Pakou HarenaDepartment of History and Archaeology, University of Lomé, Lomé, Togo.
Lebarama BakrobenaDepartment of History and Archaeology, University of Lomé, Lomé, Togo.
Forka Leypey Mathew FomineDepartment of History and African Civilizations, Faculty of Arts, University of Buea, Buea, Cameroon.
Zelalem GebreMariam TolesaDepartment of Microbial Sciences and Genetics, Addis Ababa University, Addis Ababa, Ethiopia.ORCID 0000-0002-6936-4238
Wendawek Abebe MengeshaDepartment of Microbial Sciences and Genetics, Addis Ababa University, Addis Ababa, Ethiopia.ORCID 0000-0002-6426-3489
Michael de JonghDepartment of Anthropology and Archaeology, University of South Africa, Pretoria, South Africa.
Himla SoodyallDivision of Human Genetics, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Koen BostoenUGent Centre for Bantu Studies (BantUGent), Department of Languages and Cultures, Ghent University, Ghent, Belgium.ORCID 0000-0003-2284-6165
Chiara BarbieriDepartment of Life and Environmental Sciences, University of Cagliari, Monserrato, CA, Italy.ORCID 0000-0001-8827-5655
Maximilian LarenaHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8799-7645
Helena MalmströmHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-6456-8055
Carina M SchlebuschHuman Evolution, Department of Organismal Biology, Uppsala University, Uppsala, Sweden. carina.schlebusch@ebc.uu.se.ORCID 0000-0002-8160-9621

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 759933
6 · The paper itself

Abstract

Africa harbors the richest diversity of mitochondrial DNA lineages, reflecting its central role in human evolutionary history. Early studies of mtDNA variation provided the first genetic evidence for the African origin of modern humans. With complete mitochondrial genome sequencing, we can now reconstruct maternal lineages with high resolution, yet large parts of the continent remain underrepresented. Using a newly developed long-range sequencing assay, we generated 1176 complete mitochondrial genomes from 13 countries across sub-Saharan Africa, focusing on previously understudied regions. We combined these with over 3600 publicly available African mitogenomes to produce a comprehensive dataset and updated overview of maternal genetic diversity across the continent. We contextualized this diversity with autosomal structure and information on major human expansions, integrating archeological and linguistic evidence. Our analyses suggest an initial demographic expansion of Niger-Congo speakers around 17 thousand years ago (kya), and an initial  expansion associated with Bantu-speaking groups around 6 kya. We identify haplogroup L3e as a key marker of this early Bantu expansion, tracking its spread across sub-Saharan Africa. Distinct demographic signatures also emerge for different geographic sub-branches of Bantu speakers. These findings highlight the power of mitochondrial DNA to trace maternal ancestry and demographic history in Africa, while also acknowledging its limitations for phylogeographic reconstruction.

Indexed as

Black PeopleDNA, MitochondrialGenome, MitochondrialGenetics, PopulationGenetic VariationHaplotypesHumansPhylogenySub-Saharan African PeopleDNA, Mitochondrial

Identifiers

PMID42236926
PMCPMC13234189

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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.