An in-depth analysis of the mitochondrial phylogenetic landscape of Cambodia.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
24 05 2021
Historique:
received: 25 03 2021
accepted: 07 05 2021
entrez: 25 5 2021
pubmed: 26 5 2021
medline: 6 11 2021
Statut: epublish

Résumé

Cambodia harbours a variety of human aboriginal populations that have scarcely been studied in terms of genetic diversity of entire mitochondrial genomes. Here we present the matrilineal gene pool of 299 Cambodian refugees from three different ethnic groups (Cham, Khmer, and Khmer Loeu) deriving from 16 Cambodian districts. After establishing a DNA-saving high-throughput strategy for mitochondrial whole-genome Sanger sequencing, a HaploGrep based workflow was used for quality control, haplogroup classification and phylogenetic reconstruction. The application of diverse phylogenetic algorithms revealed an exciting picture of the genetic diversity of Cambodia, especially in relation to populations from Southeast Asia and from the whole world. A total of 224 unique haplotypes were identified, which were mostly classified under haplogroups B5a1, F1a1, or categorized as newly defined basal haplogroups or basal sub-branches of R, N and M clades. The presence of autochthonous maternal lineages could be confirmed as reported in previous studies. The exceptional homogeneity observed between and within the three investigated Cambodian ethnic groups indicates genetic isolation of the whole population. Between ethnicities, genetic barriers were not detected. The mtDNA data presented here increases the phylogenetic resolution in Cambodia significantly, thereby highlighting the need for an update of the current human mtDNA phylogeny.

Identifiants

pubmed: 34031453
doi: 10.1038/s41598-021-90145-2
pii: 10.1038/s41598-021-90145-2
pmc: PMC8144189
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

10816

Références

Int J Legal Med. 2008 May;122(3):257-9
pubmed: 17960413
Bioessays. 2015 Jun;37(6):584-5
pubmed: 25728033
Eur J Hum Genet. 2020 Nov;28(11):1563-1579
pubmed: 32690935
Am J Hum Genet. 2010 Dec 10;87(6):802-12
pubmed: 21129724
Nucleic Acids Res. 2019 Jul 2;47(W1):W256-W259
pubmed: 30931475
Hum Mutat. 2009 Feb;30(2):E386-94
pubmed: 18853457
BMC Bioinformatics. 2010 Mar 09;11:122
pubmed: 20214782
Nature. 2015 Oct 1;526(7571):68-74
pubmed: 26432245
Am J Hum Genet. 2012 Apr 6;90(4):675-84
pubmed: 22482806
Am J Hum Genet. 2014 May 1;94(5):721-33
pubmed: 24726474
Am J Hum Genet. 1999 Dec;65(6):1718-24
pubmed: 10577926
Am J Hum Genet. 2005 Sep;77(3):408-19
pubmed: 16080116
Am J Hum Genet. 2007 Jan;80(1):29-43
pubmed: 17160892
Am J Hum Genet. 2011 Feb 11;88(2):239-47
pubmed: 21295281
Mol Biol Evol. 1999 Jan;16(1):37-48
pubmed: 10331250
Proc Natl Acad Sci U S A. 2007 Sep 4;104(36):14277-82
pubmed: 17717084
Mol Biol Evol. 2008 Jun;25(6):1209-18
pubmed: 18359946
Sci Rep. 2018 Aug 3;8(1):11651
pubmed: 30076323
PLoS Comput Biol. 2014 Apr 10;10(4):e1003537
pubmed: 24722319
Hum Genet. 2017 Jan;136(1):85-98
pubmed: 27837350
BMC Evol Biol. 2011 Feb 18;11:49
pubmed: 21333001
Bioinformatics. 2019 Nov 1;35(21):4453-4455
pubmed: 31070718
Bioinformatics. 2011 Aug 1;27(15):2156-8
pubmed: 21653522
Mol Biol Evol. 2010 Jan;27(1):21-31
pubmed: 19755666
Int J Legal Med. 2009 Nov;123(6):495-501
pubmed: 19727793
Nucleic Acids Res. 2016 Jul 8;44(W1):W58-63
pubmed: 27084951
Nat Commun. 2013;4:2599
pubmed: 24121720
Eur J Hum Genet. 2018 Jun;26(6):898-911
pubmed: 29483671
BMC Evol Biol. 2014 Jan 28;14:17
pubmed: 24467713
Mol Biol Evol. 2006 Dec;23(12):2480-91
pubmed: 16982817
Eur J Hum Genet. 2020 May;28(5):636-645
pubmed: 31827276
Nat Genet. 1999 Oct;23(2):147
pubmed: 10508508
Genome Res. 2021 Jan 15;:
pubmed: 33452015
Science. 2009 Dec 11;326(5959):1541-5
pubmed: 20007900
Eur J Hum Genet. 2014 Feb;22(2):228-37
pubmed: 23756438

Auteurs

Anita Kloss-Brandstätter (A)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.
Carinthia University of Applied Sciences, Villach, Austria.

Monika Summerer (M)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.

David Horst (D)

Institute of Pathology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Basil Horst (B)

Department of Dermatology, Dermatopathology, Columbia University Medical Center, New York, NY, USA.
Department of Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada.

Gertraud Streiter (G)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.

Julia Raschenberger (J)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.

Florian Kronenberg (F)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria.

Torpong Sanguansermsri (T)

Thalassemia Unit, University of Phayao, Phayao, Thailand.

Jürgen Horst (J)

Institut für Humangenetik, Universität Münster, Münster, Germany.

Hansi Weissensteiner (H)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. hansi.weissensteiner@i-med.ac.at.

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Classifications MeSH