Revisiting the African mtDNA landscape through complete mitochondrial genomes
Lankheet IPapers in this archive, Chowdhury APapers in this archive, Tellgren-Roth CPapers in this archive, Jolly CPapers in this archive, Soares AERPapers in this archive, de Navascués MPapers in this archive, Pacchiarotti SPapers in this archive, Maselli LPapers in this archive, Kouarata GPapers in this archive, Donzo JPPapers in this archive, Coetzee VPapers in this archive, de Castro MPapers in this archive, Ebbesen PPapers in this archive, Priehodová EPapers in this archive, Podgorná EPapers in this archive, Černý VPapers in this archive, Green STPapers in this archive, Harena PPapers in this archive, Bakrobena LPapers in this archive, Fomine FLMPapers in this archive, Tolesa ZGPapers in this archive, Mengesha WAPapers in this archive, de Jongh MPapers in this archive, Soodyall HPapers in this archive, Bostoen KPapers in this archive, Barbieri CPapers in this archive, Larena MPapers in this archive, Malmström HPapers in this archive, Schlebusch CMPapers in this archive
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. Subject terms: Population genetics, Evolutionary biology
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