The Dawn of Human Matrilineal Diversity
Overview
Authors
Affiliations
The quest to explain demographic history during the early part of human evolution has been limited because of the scarce paleoanthropological record from the Middle Stone Age. To shed light on the structure of the mitochondrial DNA (mtDNA) phylogeny at the dawn of Homo sapiens, we constructed a matrilineal tree composed of 624 complete mtDNA genomes from sub-Saharan Hg L lineages. We paid particular attention to the Khoi and San (Khoisan) people of South Africa because they are considered to be a unique relic of hunter-gatherer lifestyle and to carry paternal and maternal lineages belonging to the deepest clades known among modern humans. Both the tree phylogeny and coalescence calculations suggest that Khoisan matrilineal ancestry diverged from the rest of the human mtDNA pool 90,000-150,000 years before present (ybp) and that at least five additional, currently extant maternal lineages existed during this period in parallel. Furthermore, we estimate that a minimum of 40 other evolutionarily successful lineages flourished in sub-Saharan Africa during the period of modern human dispersal out of Africa approximately 60,000-70,000 ybp. Only much later, at the beginning of the Late Stone Age, about 40,000 ybp, did introgression of additional lineages occur into the Khoisan mtDNA pool. This process was further accelerated during the recent Bantu expansions. Our results suggest that the early settlement of humans in Africa was already matrilineally structured and involved small, separately evolving isolated populations.
Moutsouri I, Manoli P, Christofi V, Bashiardes E, Keravnou A, Xenophontos S PLoS One. 2024; 19(2):e0292790.
PMID: 38315645 PMC: 10843121. DOI: 10.1371/journal.pone.0292790.
Havas Augustin D, Sarac J, Reidla M, Tamm E, Grahovac B, Kapovic M Genes (Basel). 2023; 14(8).
PMID: 37628665 PMC: 10454736. DOI: 10.3390/genes14081614.
The genomic origin of Zana of Abkhazia.
Margaryan A, Sinding M, Caroe C, Yamshchikov V, Burtsev I, Gilbert M Adv Genet (Hoboken). 2023; 2(2):e10051.
PMID: 36618122 PMC: 9744565. DOI: 10.1002/ggn2.10051.
Mitochondrial DNA haplogroup, genetic ancestry, and susceptibility to Ewing sarcoma.
Kaneva K, Schurr T, Tatarinova T, Buckley J, Merkurjev D, Triska P Mitochondrion. 2022; 67:6-14.
PMID: 36115539 PMC: 9997094. DOI: 10.1016/j.mito.2022.09.002.
Maier P, Runfeldt G, Estes R, Vilar M Sci Rep. 2022; 12(1):10747.
PMID: 35750688 PMC: 9232647. DOI: 10.1038/s41598-022-13856-0.