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      Aboriginal Australian mitochondrial genome variation – an increased understanding of population antiquity and diversity

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          Abstract

          Aboriginal Australians represent one of the oldest continuous cultures outside Africa, with evidence indicating that their ancestors arrived in the ancient landmass of Sahul (present-day New Guinea and Australia) ~55 thousand years ago. Genetic studies, though limited, have demonstrated both the uniqueness and antiquity of Aboriginal Australian genomes. We have further resolved known Aboriginal Australian mitochondrial haplogroups and discovered novel indigenous lineages by sequencing the mitogenomes of 127 contemporary Aboriginal Australians. In particular, the more common haplogroups observed in our dataset included M42a, M42c, S, P5 and P12, followed by rarer haplogroups M15, M16, N13, O, P3, P6 and P8. We propose some major phylogenetic rearrangements, such as in haplogroup P where we delinked P4a and P4b and redefined them as P4 (New Guinean) and P11 (Australian), respectively. Haplogroup P2b was identified as a novel clade potentially restricted to Torres Strait Islanders. Nearly all Aboriginal Australian mitochondrial haplogroups detected appear to be ancient, with no evidence of later introgression during the Holocene. Our findings greatly increase knowledge about the geographic distribution and phylogenetic structure of mitochondrial lineages that have survived in contemporary descendants of Australia’s first settlers.

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          A revised timescale for human evolution based on ancient mitochondrial genomes.

          Recent analyses of de novo DNA mutations in modern humans have suggested a nuclear substitution rate that is approximately half that of previous estimates based on fossil calibration. This result has led to suggestions that major events in human evolution occurred far earlier than previously thought. Here, we use mitochondrial genome sequences from ten securely dated ancient modern humans spanning 40,000 years as calibration points for the mitochondrial clock, thus yielding a direct estimate of the mitochondrial substitution rate. Our clock yields mitochondrial divergence times that are in agreement with earlier estimates based on calibration points derived from either fossils or archaeological material. In particular, our results imply a separation of non-Africans from the most closely related sub-Saharan African mitochondrial DNAs (haplogroup L3) that occurred less than 62-95 kya. Though single loci like mitochondrial DNA (mtDNA) can only provide biased estimates of population divergence times, they can provide valid upper bounds. Our results exclude most of the older dates for African and non-African population divergences recently suggested by de novo mutation rate estimates in the nuclear genome. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Mitochondrial genome variation and the origin of modern humans.

            The analysis of mitochondrial DNA (mtDNA) has been a potent tool in our understanding of human evolution, owing to characteristics such as high copy number, apparent lack of recombination, high substitution rate and maternal mode of inheritance. However, almost all studies of human evolution based on mtDNA sequencing have been confined to the control region, which constitutes less than 7% of the mitochondrial genome. These studies are complicated by the extreme variation in substitution rate between sites, and the consequence of parallel mutations causing difficulties in the estimation of genetic distance and making phylogenetic inferences questionable. Most comprehensive studies of the human mitochondrial molecule have been carried out through restriction-fragment length polymorphism analysis, providing data that are ill suited to estimations of mutation rate and therefore the timing of evolutionary events. Here, to improve the information obtained from the mitochondrial molecule for studies of human evolution, we describe the global mtDNA diversity in humans based on analyses of the complete mtDNA sequence of 53 humans of diverse origins. Our mtDNA data, in comparison with those of a parallel study of the Xq13.3 region in the same individuals, provide a concurrent view on human evolution with respect to the age of modern humans.
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              An Aboriginal Australian genome reveals separate human dispersals into Asia.

              We present an Aboriginal Australian genomic sequence obtained from a 100-year-old lock of hair donated by an Aboriginal man from southern Western Australia in the early 20th century. We detect no evidence of European admixture and estimate contamination levels to be below 0.5%. We show that Aboriginal Australians are descendants of an early human dispersal into eastern Asia, possibly 62,000 to 75,000 years ago. This dispersal is separate from the one that gave rise to modern Asians 25,000 to 38,000 years ago. We also find evidence of gene flow between populations of the two dispersal waves prior to the divergence of Native Americans from modern Asian ancestors. Our findings support the hypothesis that present-day Aboriginal Australians descend from the earliest humans to occupy Australia, likely representing one of the oldest continuous populations outside Africa.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                13 March 2017
                2017
                : 7
                : 43041
                Affiliations
                [1 ]Department of Biochemistry and Genetics, La Trobe Institute for Molecular Sciences, La Trobe University , Melbourne, Victoria, Australia
                [2 ]Department of Genetic Identification, Erasmus MC University Medical Center Rotterdam , The Netherlands
                [3 ]Australian Genome Research Facility , Melbourne, Victoria, Australia
                [4 ]Biotechnology and Biomolecular Sciences, University of New South Wales , New South Wales, Australia
                [5 ]School of Biological Sciences, University of Sydney , Sydney, Australia
                [6 ]The Wellcome Trust Sanger Institute, Welcome Trust Genome Campus , Hinxton, Cambridgeshire, United Kingdom
                [7 ]Office of the Chief Forensic Scientist, Victoria Police Forensic Services Department , Melbourne, Victoria, Australia
                [8 ]Griffith University , Queensland, Australia
                [9 ]Community Elder and Cultural Advisor , Brisbane, Queensland, Australia
                [10 ]Madurai Kamaraj University , Madurai, Tamil Nadu, India
                [11 ]University of Adelaide , South Australia, Australia
                [12 ]Research Centre for Medical Genetics, Russian Academy of Medical Sciences , Moscow, Russia
                [13 ]Universitat Pompeu Fabra , Barcelona, Spain
                [14 ]University of Otago , Dunedin, New Zealand
                [15 ]Department of Anthropology, University of Pennsylvania , PA, USA
                [16 ]Lebanese American University , Chouran, Beirut, Lebanon
                [17 ]National Health Laboratory Service , Johannesburg, South Africa
                [18 ]IBM, Yorktown Heights , NY, USA
                [19 ]Fudan University , Shanghai, China
                [20 ]University of Arizona , Tucson, AZ, USA
                [21 ]Institut Pasteur , Paris, France
                [22 ]University of Cambridge , Cambridge, United Kingdom
                [23 ]Universidade Federal de Minas Gerais , Belo Horizonte, Minas Gerais, Brazil
                [24 ]National Geographic Society , Washington, DC, USA
                [25 ]IBM, Somers , NY, USA
                [26 ]Applied Biosystems , Foster City, CA, USA
                Author notes
                Article
                srep43041
                10.1038/srep43041
                5347126
                28287095
                1d4272ed-4a7f-4d40-b02e-fc1586c03a6a
                Copyright © 2017, The Author(s)

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 11 October 2016
                : 17 January 2017
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