Aboriginal Australian Mitochondrial Genome Variation
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Y-Chromosome and Surname Analyses for Reconstructing Past Population Structures: the Sardinian Population As a Test Case
International Journal of Molecular Sciences Article Y-chromosome and Surname Analyses for Reconstructing Past Population Structures: The Sardinian Population as a Test Case Viola Grugni 1, Alessandro Raveane 1, Giulia Colombo 1, Carmen Nici 1, Francesca Crobu 1,2, Linda Ongaro 1,3,4, Vincenza Battaglia 1, Daria Sanna 1,5, Nadia Al-Zahery 1, Ornella Fiorani 6, Antonella Lisa 6, Luca Ferretti 1 , Alessandro Achilli 1, Anna Olivieri 1, Paolo Francalacci 7, Alberto Piazza 8, Antonio Torroni 1 and Ornella Semino 1,* 1 Dipartimento di Biologia e Biotecnologie “L. Spallanzani”, Università di Pavia, 27100 Pavia, Italy; [email protected] (V.G.); [email protected] (A.R.); [email protected] (G.C.); [email protected] (C.N.); [email protected] (F.C.); [email protected] (L.O.); [email protected] (V.B.); [email protected] (D.S.); [email protected] (N.A.-Z.); [email protected] (L.F.); [email protected] (A.A.); [email protected] (A.O.); [email protected] (A.T.) 2 Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche (CNR), 09042 Monserrato, Italy 3 Estonian Biocentre, Institute of Genomics, Riia 23, 51010 Tartu, Estonia 4 Department of Evolutionary Biology, Institute of Molecular and Cell Biology, Riia 23, 51010 Tartu, Estonia 5 Dipartimento di Scienze Biomediche, Università di Sassari, 07100 Sassari, Italy 6 Istituto di Genetica Molecolare “L.L. Cavalli-Sforza”, Consiglio Nazionale delle Ricerche (CNR), 27100 Pavia, Italy; fi[email protected] -
An Overview of the Independent Histories of the Human Y Chromosome and the Human Mitochondrial Chromosome
The Proceedings of the International Conference on Creationism Volume 8 Print Reference: Pages 133-151 Article 7 2018 An Overview of the Independent Histories of the Human Y Chromosome and the Human Mitochondrial chromosome Robert W. Carter Stephen Lee University of Idaho John C. Sanford Cornell University, Cornell University College of Agriculture and Life Sciences School of Integrative Plant Science,Follow this Plant and Biology additional Section works at: https://digitalcommons.cedarville.edu/icc_proceedings DigitalCommons@Cedarville provides a publication platform for fully open access journals, which means that all articles are available on the Internet to all users immediately upon publication. However, the opinions and sentiments expressed by the authors of articles published in our journals do not necessarily indicate the endorsement or reflect the views of DigitalCommons@Cedarville, the Centennial Library, or Cedarville University and its employees. The authors are solely responsible for the content of their work. Please address questions to [email protected]. Browse the contents of this volume of The Proceedings of the International Conference on Creationism. Recommended Citation Carter, R.W., S.S. Lee, and J.C. Sanford. An overview of the independent histories of the human Y- chromosome and the human mitochondrial chromosome. 2018. In Proceedings of the Eighth International Conference on Creationism, ed. J.H. Whitmore, pp. 133–151. Pittsburgh, Pennsylvania: Creation Science Fellowship. Carter, R.W., S.S. Lee, and J.C. Sanford. An overview of the independent histories of the human Y-chromosome and the human mitochondrial chromosome. 2018. In Proceedings of the Eighth International Conference on Creationism, ed. J.H. -
Mitochondrial DNA Diversity of Present-Day Aboriginal Australians and Implications for Human Evolution in Oceania
Journal of Human Genetics (2016), 1–11 & 2016 The Japan Society of Human Genetics All rights reserved 1434-5161/16 www.nature.com/jhg ORIGINAL ARTICLE Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania Nano Nagle1, Kaye N Ballantyne2,3, Mannis van Oven3, Chris Tyler-Smith4, Yali Xue4, Stephen Wilcox5, Leah Wilcox1, Rust Turkalov5, Roland AH van Oorschot2, Sheila van Holst Pellekaan6,7, Theodore G Schurr8, Peter McAllister9, Lesley Williams10, Manfred Kayser3, R John Mitchell1 and The Genographic Consortium27 Aboriginal Australians are one of the more poorly studied populations from the standpoint of human evolution and genetic diversity. Thus, to investigate their genetic diversity, the possible date of their ancestors’ arrival and their relationships with neighboring populations, we analyzed mitochondrial DNA (mtDNA) diversity in a large sample of Aboriginal Australians. Selected mtDNA single-nucleotide polymorphisms and the hypervariable segment haplotypes were analyzed in 594 Aboriginal Australians drawn from locations across the continent, chiefly from regions not previously sampled. Most (~78%) samples could be assigned to mtDNA haplogroups indigenous to Australia. The indigenous haplogroups were all ancient (with estimated ages 440 000 years) and geographically widespread across the continent. The most common haplogroup was P (44%) followed by S (23%) and M42a (9%). There was some geographic structure at the haplotype level. The estimated ages of the indigenous haplogroups range from 39 000 to 55 000 years, dates that fit well with the estimated date of colonization of Australia based on archeological evidence (~47 000 years ago). The distribution of mtDNA haplogroups in Australia and New Guinea supports the hypothesis that the ancestors of Aboriginal Australians entered Sahul through at least two entry points. -
The Enigmatic Origin of Bovine Mtdna Haplogroup R: Sporadic Interbreeding Or an Independent Event of Bos Primigenius Domestication in Italy?
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by PubMed Central The Enigmatic Origin of Bovine mtDNA Haplogroup R: Sporadic Interbreeding or an Independent Event of Bos primigenius Domestication in Italy? Silvia Bonfiglio1, Alessandro Achilli1,2, Anna Olivieri1, Riccardo Negrini3, Licia Colli3, Luigi Liotta4, Paolo Ajmone-Marsan3, Antonio Torroni1, Luca Ferretti1* 1 Dipartimento di Genetica e Microbiologia, Universita` di Pavia, Pavia, Italy, 2 Dipartimento di Biologia Cellulare e Ambientale, Universita` di Perugia, Perugia, Italy, 3 Istituto di Zootecnica, Universita` Cattolica del Sacro Cuore, Piacenza, Italy, 4 Dipartimento di Morfologia, Biochimica, Fisiologia e Produzioni Animali, Universita` di Messina, Messina, Italy Abstract Background: When domestic taurine cattle diffused from the Fertile Crescent, local wild aurochsen (Bos primigenius) were still numerous. Moreover, aurochsen and introduced cattle often coexisted for millennia, thus providing potential conditions not only for spontaneous interbreeding, but also for pastoralists to create secondary domestication centers involving local aurochs populations. Recent mitochondrial genomes analyses revealed that not all modern taurine mtDNAs belong to the shallow macro-haplogroup T of Near Eastern origin, as demonstrated by the detection of three branches (P, Q and R) radiating prior to the T node in the bovine phylogeny. These uncommon haplogroups represent excellent tools to evaluate if sporadic interbreeding or even additional events of cattle domestication occurred. Methodology: The survey of the mitochondrial DNA (mtDNA) control-region variation of 1,747 bovine samples (1,128 new and 619 from previous studies) belonging to 37 European breeds allowed the identification of 16 novel non-T mtDNAs, which after complete genome sequencing were confirmed as members of haplogroups Q and R. -
Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups
doi: 10.1046/j.1529-8817.2003.00127.x Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups Elena B. Starikovskaya1, Rem I. Sukernik1† Olga A. Derbeneva1,2, Natalia V. Volodko1, ∗ Eduardo Ruiz-Pesini2, Antonio Torroni3, Michael D. Brown2 , Marie T. Lott2, Seyed H. Hosseini2, Kirsi Huoponen4, and Douglas C. Wallace2† 1Laboratory of Human Molecular Genetics, Institute of Cytology and Genetics, Siberian Division, Russian Academy of Sciences, Novosibirsk, 2Center for Molecular Medicine, Emory University, Atlanta, GA, 3Dipartimento di Genetica e Microbiologia, Universit di Pavia, Pavia, Italy, 4Department of Medical Genetics, University in Turku, Finland Summary In search of the ancestors of Native American mitochondrial DNA (mtDNA) haplogroups, we analyzed the mtDNA of 531 individuals from nine indigenous populations in Siberia. All mtDNAs were subjected to high-resolution RFLP analysis, sequencing of the control-region hypervariable segment I (HVS-I), and surveyed for additional polymorphic markers in the coding region. Furthermore, the mtDNAs selected according to haplogroup/subhaplogroup status were completely sequenced. Phylogenetic analyses of the resulting data, combined with those from previously published Siberian arctic and sub-arctic populations, revealed that remnants of the ancient Siberian gene pool are still evident in Siberian populations, suggesting that the founding haplotypes of the Native American A-D branches originated in different parts of Siberia. Thus, lineage A complete sequences revealed in the Mansi of the Lower Ob and the Ket of the Lower Yenisei belong to A1, suggesting that A1 mtDNAs occasionally found in the remnants of hunting-gathering populations of northwestern and northern Siberia belonged to a common gene pool of the Siberian progenitors of Paleoindians. -
Cattle Mitogenome Variation Reveals a Post-Glacial Expansion Of
www.nature.com/scientificreports OPEN Cattle mitogenome variation reveals a post‑glacial expansion of haplogroup P and an early incorporation into northeast Asian domestic herds Hideyuki Mannen1,4*, Takahiro Yonezawa2,4, Kako Murata1, Aoi Noda1, Fuki Kawaguchi1, Shinji Sasazaki1, Anna Olivieri3, Alessandro Achilli3 & Antonio Torroni3 Surveys of mitochondrial DNA (mtDNA) variation have shown that worldwide domestic cattle are characterized by just a few major haplogroups. Two, T and I, are common and characterize Bos taurus and Bos indicus, respectively, while the other three, P, Q and R, are rare and are found only in taurine breeds. Haplogroup P is typical of extinct European aurochs, while intriguingly modern P mtDNAs have only been found in northeast Asian cattle. These Asian P mtDNAs are extremely rare with the exception of the Japanese Shorthorn breed, where they reach a frequency of 45.9%. To shed light on the origin of this haplogroup in northeast Asian cattle, we completely sequenced 14 Japanese Shorthorn mitogenomes belonging to haplogroup P. Phylogenetic and Bayesian analyses revealed: (1) a post‑glacial expansion of aurochs carrying haplogroup P from Europe to Asia; (2) that all Asian P mtDNAs belong to a single sub‑haplogroup (P1a), so far never detected in either European or Asian aurochs remains, which was incorporated into domestic cattle of continental northeastern Asia possibly ~ 3700 years ago; and (3) that haplogroup P1a mtDNAs found in the Japanese Shorthorn breed probably reached Japan about 650 years ago from Mongolia/Russia, in agreement with historical evidence. All modern cattle derive from wild ancestral aurochs (Bos primigenius), which were distributed throughout large parts of Eurasia and Northern Africa during the Pleistocene and the early Holocene1,2. -
Y Chromosomes of 40% Chinese Are Descendants of Three Neolithic
Title: Y Chromosomes of 40% Chinese Are Descendants of Three Neolithic Super-grandfathers Authors: Shi Yan1,2*, Chuan-Chao Wang1, Hong-Xiang Zheng1, Wei Wang2, Zhen-Dong Qin1, Lan-Hai Wei1, Yi Wang1, Xue-Dong Pan1, Wen-Qing Fu1,4, Yun-Gang He2, Li-Jun Xiong4, Wen-Fei Jin2, Shi-Lin Li1, Yu An1, Hui Li1, Li Jin1,2* Affiliations 1Ministry of Education Key Laboratory of Contemporary Anthropology and Center for Evolutionary Biology, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China. 2Chinese Academy of Sciences Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, SIBS, CAS, Shanghai 200031, China. 3Epigenetics Laboratory, Institute of Biomedical Sciences, Fudan University, Shanghai 200032, China. 4Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA *Correspondence to: L. J. ([email protected]) or S. Y. ([email protected]). Abstract: Demographic change of human populations is one of the central questions for delving into the past of human beings. To identify major population expansions related to male lineages, we sequenced 78 East Asian Y chromosomes at 3.9 Mbp of the non-recombining region (NRY), discovered >4,000 new SNPs, and identified many new clades. The relative divergence dates can be estimated much more precisely using molecular clock. We found that all the Paleolithic divergences were binary; however, three strong star-like Neolithic expansions at ~6 kya (thousand years ago) (assuming a constant substitution rate of 1×10-9 /bp/year) indicates that ~40% of modern Chinese are patrilineal descendants of only three super-grandfathers at that time. -
Mitochondrial Genetic Diversity and Its Determinants in Island Melanesia
University of Pennsylvania ScholarlyCommons Department of Anthropology Papers Department of Anthropology 2005 Mitochondrial Genetic Diversity and its Determinants in Island Melanesia Jonathan S. Friedlaender Fred Gentz Françoise R. Friedlaender Frederika Kaestle Theodore G. Schurr University of Pennsylvania, [email protected] See next page for additional authors Follow this and additional works at: https://repository.upenn.edu/anthro_papers Part of the Anthropology Commons, and the Genetics Commons Recommended Citation (OVERRIDE) Friedlaender, J. et al., (2005). Mitochondrial Genetic Diversity and its Determinants in Island Melanesia. In A. Pawley, R. Attenborough, J. Golson, and R. Hide (Eds.), Papun Pasts: Cultural, Linguistic, and Biological Histories Of Papuan-Speaking Peoples (693-716). Canberra: Pacific Linguistics. This paper is posted at ScholarlyCommons. https://repository.upenn.edu/anthro_papers/163 For more information, please contact [email protected]. Mitochondrial Genetic Diversity and its Determinants in Island Melanesia Abstract For a long time, many physical anthropologists and human geneticists considered Island Melanesian populations to be genetically impoverished, dominated by the effects of random genetic drift because of their small sizes, internally very homogeneous, and therefore of little relevance in reconstructing past human migrations. This view is changing. Here we present the developing detailed picture of mitochondrial DNA (mtDNA) variation in eastern New Guinea and Island Melanesia that reflects linguistic distinctions within the region as well as considerable island-by-island isolation. It also appears that the patterns of variation reflect marital migration distinctions between bush and beach populations. We have identified a number of egionallyr specific mtDNA variants. We also question the widely accepted hypothesis that the mtDNA variant referred to as the ‘Polynesian Motif’ (or alternatively the ‘Austronesian Motif’) developed outside this region somewhere to the west. -
An Unbiased Resource of Novel SNP Markers Provides a New Chronology for the Human Y Chromosome and Reveals a Deep Phylogenetic Structure in Africa
Downloaded from genome.cshlp.org on October 2, 2021 - Published by Cold Spring Harbor Laboratory Press An unbiased resource of novel SNP markers provides a new chronology for the human Y chromosome and reveals a deep phylogenetic structure in Africa Rosaria Scozzari,1 Andrea Massaia,1 Beniamino Trombetta,1 Giovanna Bellusci,2 Natalie M. Myres,3,4 Andrea Novelletto,2,* Fulvio Cruciani1,* 1Dipartimento di Biologia e Biotecnologie “C. Darwin”, Sapienza Università di Roma, Rome 00185, Italy; 2Dipartimento di Biologia, Università di Roma “Tor Vergata”, Rome 00133, Italy; 3AncestryDNA, Provo, UT 84604, USA; 4Sorenson Molecular Genealogy Foundation, Salt Lake City, UT 84115, USA *Correspondence: [email protected] (A.N.), [email protected] (F.C.) Andrea Novelletto, Dipartimento di Biologia, Università di Roma “Tor Vergata”, Rome 00133, Italy; Phone: ++39 06 72594104 Fax: ++39 06 2023500 email: [email protected] Fulvio Cruciani Dipartimento di Biologia e Biotecnologie “C. Darwin”, Sapienza Università di Roma, Rome 00185, Italy Phone: ++39 06 49912857 Fax: ++39 06 4456866 email:[email protected] Running title: Deep rooted human Y chromosomes Keywords: Human MSY phylogeny; Molecular dating; Targeted next generation sequencing; Y chromosome sequence diversity; Out of Africa. Downloaded from genome.cshlp.org on October 2, 2021 - Published by Cold Spring Harbor Laboratory Press Abstract The phylogeography of the paternally-inherited MSY has been the subject of intense research. However, sequence diversity and the ages of the deepest nodes of the phylogeny remain largely unexplored due to the severely biased collection of SNPs available for study. We characterized 68 worldwide Y chromosomes by high-coverage next generation sequencing, including 18 deep- rooting ones, and identified 2,386 SNPs, 80% of which were novel. -
A Globally Diverse Reference Alignment and Panel for Imputation of Mitochondrial DNA Variants
bioRxiv preprint doi: https://doi.org/10.1101/649293; this version posted December 23, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. A globally diverse reference alignment and panel for imputation of mitochondrial DNA variants Tim W McInerney1, Brian Fulton-Howard2, Christopher Patterson3,4, Devashi Paliwal1, Lars S Jermiin5,6,7,8, Hardip R Patel1, Judy Pa3,4, Russell H Swerdlow9, Alison Goate2, Simon Easteal1, Shea J Andrews2*, for the Alzheimer’s Disease Neuroimaging Initiative† 1John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia 2Ronald M. Loeb Center for Alzheimer’s Disease, Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York City, NY, USA 3Mark and Mary Stevens Neuroimaging and Informatics Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA 4Department of Neurology, Alzheimer’s Disease Research Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA 5CSIRO Land & Water, Commonwealth Scientific Industrial & Research Organization, Acton, ACT 2601, Australia 6Research School of Biology, Australian National University, Canberra, ACT 2601, Australia 7School of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland 8Earth Institute, University College Dublin, Belfield, Dublin 4, Ireland 9Department of Neurology, Alzheimer’s Disease Center, University of Kansas, Fairway, KS, USA bioRxiv preprint doi: https://doi.org/10.1101/649293; this version posted December 23, 2020. -
The Australian Barrineans and Their Relationship to Southeast Asian
Human Biology Volume 85 Issue 1 Special Issue on Revisiting the "Negrito" Article 21 Hypothesis 2013 The Australian Barrineans and Their Relationship to Southeast Asian Negritos: An Investigation using Mitochondrial Genomics Peter McAllister PERAHU, School of Humanities, Gold Coast Campus, Griffith University, Queensland, Australia, [email protected] Nano Nagle Department of Genetics, La Trobe University, Victoria, Australia Robert John Mitchell Department of Genetics, La Trobe University, Victoria, Australia Follow this and additional works at: http://digitalcommons.wayne.edu/humbiol Part of the Biological and Physical Anthropology Commons, and the Genetics and Genomics Commons Recommended Citation McAllister, Peter; Nagle, Nano; and Mitchell, Robert John (2013) "The Australian Barrineans and Their Relationship to Southeast Asian Negritos: An Investigation using Mitochondrial Genomics," Human Biology: Vol. 85: Iss. 1, Article 21. Available at: http://digitalcommons.wayne.edu/humbiol/vol85/iss1/21 The Australian Barrineans and Their Relationship to Southeast Asian Negritos: An Investigation using Mitochondrial Genomics Abstract The existence of a short-statured Aboriginal population in the Far North Queensland (FNQ) rainforest zone of Australia’s northeast coast and Tasmania has long been an enigma in Australian anthropology. Based on their reduced stature and associated morphological traits such as tightly curled hair, Birdsell and Tindale proposed that these "Barrinean" peoples were closely related to "negrito" peoples of -
The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint
Review of Books on the Book of Mormon 1989–2011 Volume 22 Number 1 Article 9 2010 The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint Ugo. A. Perego Follow this and additional works at: https://scholarsarchive.byu.edu/msr BYU ScholarsArchive Citation Perego, Ugo. A. (2010) "The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint," Review of Books on the Book of Mormon 1989–2011: Vol. 22 : No. 1 , Article 9. Available at: https://scholarsarchive.byu.edu/msr/vol22/iss1/9 This Book of Mormon is brought to you for free and open access by the Journals at BYU ScholarsArchive. It has been accepted for inclusion in Review of Books on the Book of Mormon 1989–2011 by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Title The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint Author(s) Ugo A. Perego Reference FARMS Review 22/1 (2010): 191–227. ISSN 1550-3194 (print), 2156-8049 (online) Abstract The church advocates no official position on the origins of Amerindian populations. Critics and sup- porters of the Book of Mormon both attempt to bol- ster their own arguments with DNA evidence. This study reviews the properties of mitochondrial DNA (mtDNA), particularly pertaining to the origins of Native American populations. DNA studies are subject to numerous limitations. The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint Ugo.