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The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt

Takabuti, was a female who lived in ancient Egypt during the 25th Dynasty, c.660 BCE. Her mummified remains were brought to Belfast, Northern Ireland, in 1834 and are currently displayed in the Ulster Museum. To gain insight into Takabuti’s ancestry, we used deep sampling of vertebral bone, under X-...

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Autores principales: Drosou, Konstantina, Collin, Thomas C., Freeman, Peter J., Loynes, Robert, Freemont, Tony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550590/
https://www.ncbi.nlm.nih.gov/pubmed/33046824
http://dx.doi.org/10.1038/s41598-020-74114-9
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author Drosou, Konstantina
Collin, Thomas C.
Freeman, Peter J.
Loynes, Robert
Freemont, Tony
author_facet Drosou, Konstantina
Collin, Thomas C.
Freeman, Peter J.
Loynes, Robert
Freemont, Tony
author_sort Drosou, Konstantina
collection PubMed
description Takabuti, was a female who lived in ancient Egypt during the 25th Dynasty, c.660 BCE. Her mummified remains were brought to Belfast, Northern Ireland, in 1834 and are currently displayed in the Ulster Museum. To gain insight into Takabuti’s ancestry, we used deep sampling of vertebral bone, under X-ray control, to obtain non-contaminated bone tissue from which we extracted ancient DNA (aDNA) using established protocols. We targeted the maternally inherited mitochondrial DNA (mtDNA), known to be highly informative for human ancestry, and identified 38 single nucleotide variants using next generation sequencing. The specific combination of these SNVs suggests that Takabuti belonged to mitochondrial haplogroup H4a1. Neither H4 nor H4a1 have been reported in ancient Egyptian samples, prior to this study. The modern distribution of H4a1 is rare and sporadic and has been identified in areas including the Canary Islands, southern Iberia and the Lebanon. H4a1 has also been reported in ancient samples from Bell Beaker and Unetice contexts in Germany, as well as Bronze Age Bulgaria. We believe that this is an important finding because first, it adds to the depth of knowledge about the distribution of the H4a1 haplogroup in existing mtDNA, thus creating a baseline for future occurrences of this haplogroup in ancient Egyptian remains. Second, it is of great importance for archaeological sciences, since a predominantly European haplogroup has been identified in an Egyptian individual in Southern Egypt, prior to the Roman and Greek influx (332BCE).
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spelling pubmed-75505902020-10-14 The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt Drosou, Konstantina Collin, Thomas C. Freeman, Peter J. Loynes, Robert Freemont, Tony Sci Rep Article Takabuti, was a female who lived in ancient Egypt during the 25th Dynasty, c.660 BCE. Her mummified remains were brought to Belfast, Northern Ireland, in 1834 and are currently displayed in the Ulster Museum. To gain insight into Takabuti’s ancestry, we used deep sampling of vertebral bone, under X-ray control, to obtain non-contaminated bone tissue from which we extracted ancient DNA (aDNA) using established protocols. We targeted the maternally inherited mitochondrial DNA (mtDNA), known to be highly informative for human ancestry, and identified 38 single nucleotide variants using next generation sequencing. The specific combination of these SNVs suggests that Takabuti belonged to mitochondrial haplogroup H4a1. Neither H4 nor H4a1 have been reported in ancient Egyptian samples, prior to this study. The modern distribution of H4a1 is rare and sporadic and has been identified in areas including the Canary Islands, southern Iberia and the Lebanon. H4a1 has also been reported in ancient samples from Bell Beaker and Unetice contexts in Germany, as well as Bronze Age Bulgaria. We believe that this is an important finding because first, it adds to the depth of knowledge about the distribution of the H4a1 haplogroup in existing mtDNA, thus creating a baseline for future occurrences of this haplogroup in ancient Egyptian remains. Second, it is of great importance for archaeological sciences, since a predominantly European haplogroup has been identified in an Egyptian individual in Southern Egypt, prior to the Roman and Greek influx (332BCE). Nature Publishing Group UK 2020-10-12 /pmc/articles/PMC7550590/ /pubmed/33046824 http://dx.doi.org/10.1038/s41598-020-74114-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Drosou, Konstantina
Collin, Thomas C.
Freeman, Peter J.
Loynes, Robert
Freemont, Tony
The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title_full The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title_fullStr The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title_full_unstemmed The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title_short The first reported case of the rare mitochondrial haplotype H4a1 in ancient Egypt
title_sort first reported case of the rare mitochondrial haplotype h4a1 in ancient egypt
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550590/
https://www.ncbi.nlm.nih.gov/pubmed/33046824
http://dx.doi.org/10.1038/s41598-020-74114-9
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