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A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels

Polymorphic markers on the male-specific part of the Y chromosome (MSY) provide useful information for tracking male genealogies. While maternal lineages are well studied in Old World camelids using mitochondrial DNA, the lack of a Y-chromosomal reference sequence hampers the analysis of male-driven...

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Autores principales: Felkel, Sabine, Wallner, Barbara, Chuluunbat, Battsesteg, Yadamsuren, Adiya, Faye, Bernard, Brem, Gottfried, Walzer, Chris, Burger, Pamela A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537670/
https://www.ncbi.nlm.nih.gov/pubmed/31178891
http://dx.doi.org/10.3389/fgene.2019.00423
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author Felkel, Sabine
Wallner, Barbara
Chuluunbat, Battsesteg
Yadamsuren, Adiya
Faye, Bernard
Brem, Gottfried
Walzer, Chris
Burger, Pamela A.
author_facet Felkel, Sabine
Wallner, Barbara
Chuluunbat, Battsesteg
Yadamsuren, Adiya
Faye, Bernard
Brem, Gottfried
Walzer, Chris
Burger, Pamela A.
author_sort Felkel, Sabine
collection PubMed
description Polymorphic markers on the male-specific part of the Y chromosome (MSY) provide useful information for tracking male genealogies. While maternal lineages are well studied in Old World camelids using mitochondrial DNA, the lack of a Y-chromosomal reference sequence hampers the analysis of male-driven demographics. Recently, a shotgun assembly of the horse MSY was generated based on short read next generation sequencing data. The haplotype network resulting from single copy MSY variants using the assembly as a reference revealed sufficient resolution to trace individual male lines in this species. In a similar approach we generated a 3.8 Mbp sized assembly of the MSY of Camelus bactrianus. The camel MSY assembly was used as a reference for variant calling using short read data from eight Old World camelid individuals. Based on 596 single nucleotide variants we revealed a Y-phylogenetic network with seven haplotypes. Wild and domestic Bactrian camels were clearly separated into two different haplogroups with an estimated divergence time of 26,999 ± 2,268 years. Unexpectedly, one wild camel clustered into the domestic Bactrian camels’ haplogroup. The observation of a domestic paternal lineage within the wild camel population is concerning in view of the importance to conserve the genetic integrity of these highly endangered species in their natural habitat.
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spelling pubmed-65376702019-06-07 A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels Felkel, Sabine Wallner, Barbara Chuluunbat, Battsesteg Yadamsuren, Adiya Faye, Bernard Brem, Gottfried Walzer, Chris Burger, Pamela A. Front Genet Genetics Polymorphic markers on the male-specific part of the Y chromosome (MSY) provide useful information for tracking male genealogies. While maternal lineages are well studied in Old World camelids using mitochondrial DNA, the lack of a Y-chromosomal reference sequence hampers the analysis of male-driven demographics. Recently, a shotgun assembly of the horse MSY was generated based on short read next generation sequencing data. The haplotype network resulting from single copy MSY variants using the assembly as a reference revealed sufficient resolution to trace individual male lines in this species. In a similar approach we generated a 3.8 Mbp sized assembly of the MSY of Camelus bactrianus. The camel MSY assembly was used as a reference for variant calling using short read data from eight Old World camelid individuals. Based on 596 single nucleotide variants we revealed a Y-phylogenetic network with seven haplotypes. Wild and domestic Bactrian camels were clearly separated into two different haplogroups with an estimated divergence time of 26,999 ± 2,268 years. Unexpectedly, one wild camel clustered into the domestic Bactrian camels’ haplogroup. The observation of a domestic paternal lineage within the wild camel population is concerning in view of the importance to conserve the genetic integrity of these highly endangered species in their natural habitat. Frontiers Media S.A. 2019-05-21 /pmc/articles/PMC6537670/ /pubmed/31178891 http://dx.doi.org/10.3389/fgene.2019.00423 Text en Copyright © 2019 Felkel, Wallner, Chuluunbat, Yadamsuren, Faye, Brem, Walzer and Burger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Felkel, Sabine
Wallner, Barbara
Chuluunbat, Battsesteg
Yadamsuren, Adiya
Faye, Bernard
Brem, Gottfried
Walzer, Chris
Burger, Pamela A.
A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title_full A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title_fullStr A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title_full_unstemmed A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title_short A First Y-Chromosomal Haplotype Network to Investigate Male-Driven Population Dynamics in Domestic and Wild Bactrian Camels
title_sort first y-chromosomal haplotype network to investigate male-driven population dynamics in domestic and wild bactrian camels
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537670/
https://www.ncbi.nlm.nih.gov/pubmed/31178891
http://dx.doi.org/10.3389/fgene.2019.00423
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