Evidence map›Paper›PMID 25807545›Full record

ArticlePloS one2015

Revised timeline and distribution of the earliest diverged human maternal lineages in southern Africa.

Eva K F Chan, Rae-Anne Hardie, Desiree C Petersen, Karen Beeson, Riana M S Bornman, Andrew B Smith, Vanessa M Hayes

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Genomic landscape of human diversity across Madagascar.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  7. 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

7 authors.

Eva K F ChanLaboratory for Human Comparative and Prostate Cancer Genomics, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, NSW, 2010, Australia; Faculty of Medicine, University of New South Wales Australia, Randwick, NSW, Australia.
Rae-Anne HardieLaboratory for Human Comparative and Prostate Cancer Genomics, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, NSW, 2010, Australia; Faculty of Medicine, University of New South Wales Australia, Randwick, NSW, Australia.
Desiree C PetersenLaboratory for Human Comparative and Prostate Cancer Genomics, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, NSW, 2010, Australia; Faculty of Medicine, University of New South Wales Australia, Randwick, NSW, Australia; J. Craig Venter Institute, 4120 Torrey Pines Road, La Jolla, California, 92037, United States of America.
Karen BeesonJ. Craig Venter Institute, 4120 Torrey Pines Road, La Jolla, California, 92037, United States of America.
Riana M S BornmanSchool of Health Systems and Public Health, University of Pretoria, Hatfield, South Africa.
Andrew B SmithDepartment of Archaeology, University of Cape Town, Rondebosch, South Africa.
Vanessa M HayesLaboratory for Human Comparative and Prostate Cancer Genomics, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, NSW, 2010, Australia; Faculty of Medicine, University of New South Wales Australia, Randwick, NSW, Australia; J. Craig Venter Institute, 4120 Torrey Pines Road, La Jolla, California, 92037, United States of America; School of Health Systems and Public Health, University of Pretoria, Hatfield, South Africa; Central Clinical School, The University of Sydney, Camperdown, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oldest extant human maternal lineages include mitochondrial haplogroups L0d and L0k found in the southern African click-speaking forager peoples broadly classified as Khoesan. Profiling these early mitochondrial lineages allows for better understanding of modern human evolution. In this study, we profile 77 new early-diverged complete mitochondrial genomes and sub-classify another 105 L0d/L0k individuals from southern Africa. We use this data to refine basal phylogenetic divergence, coalescence times and Khoesan prehistory. Our results confirm L0d as the earliest diverged lineage (∼172 kya, 95%CI: 149-199 kya), followed by L0k (∼159 kya, 95%CI: 136-183 kya) and a new lineage we name L0g (∼94 kya, 95%CI: 72-116 kya). We identify two new L0d1 subclades we name L0d1d and L0d1c4/L0d1e, and estimate L0d2 and L0d1 divergence at ∼93 kya (95%CI:76-112 kya). We concur the earliest emerging L0d1'2 sublineage L0d1b (∼49 kya, 95%CI:37-58 kya) is widely distributed across southern Africa. Concomitantly, we find the most recent sublineage L0d2a (∼17 kya, 95%CI:10-27 kya) to be equally common. While we agree that lineages L0d1c and L0k1a are restricted to contemporary inland Khoesan populations, our observed predominance of L0d2a and L0d1a in non-Khoesan populations suggests a once independent coastal Khoesan prehistory. The distribution of early-diverged human maternal lineages within contemporary southern Africans suggests a rich history of human existence prior to any archaeological evidence of migration into the region. For the first time, we provide a genetic-based evidence for significant modern human evolution in southern Africa at the time of the Last Glacial Maximum at between ∼21-17 kya, coinciding with the emergence of major lineages L0d1a, L0d2b, L0d2d and L0d2a.

Indexed as

Biological EvolutionGenome, MitochondrialPhylogenyAfrica, SouthernBlack PeopleDNA, MitochondrialFemaleGenetics, PopulationHaplotypesHumansMolecular Sequence DataDNA, Mitochondrial

Identifiers

PMID25807545
PMCPMC4373779

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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.