Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics

Abstract It is important to determine the sex of elephants from their samples—faeces from the field or seized ivory—for forensic reasons or to understand population demography and genetic structure. Molecular sexing methods developed in the last two decades have often shown limited efficiency, parti...

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Autores principales: Laetitia Aznar-Cormano, Julie Bonnald, Sabrina Krief, Nelson Guma, Régis Debruyne
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/687b8b286b4a4b7382928099b6413295
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spelling oai:doaj.org-article:687b8b286b4a4b7382928099b64132952021-12-02T18:17:42ZMolecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics10.1038/s41598-021-86010-x2045-2322https://doaj.org/article/687b8b286b4a4b7382928099b64132952021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-86010-xhttps://doaj.org/toc/2045-2322Abstract It is important to determine the sex of elephants from their samples—faeces from the field or seized ivory—for forensic reasons or to understand population demography and genetic structure. Molecular sexing methods developed in the last two decades have often shown limited efficiency, particularly in terms of sensitivity and specificity, due to the degradation of DNA in these samples. These limitations have also prevented their use with ancient DNA samples of elephants or mammoths. Here we propose a novel TaqMan-MGB qPCR assay to address these difficulties. We designed it specifically to allow the characterization of the genetic sex for highly degraded samples of all elephantine taxa (elephants and mammoths). In vitro experiments demonstrated a high level of sensitivity and low contamination risks. We applied this assay in two actual case studies where it consistently recovered the right genotype for specimens of known sex a priori. In the context of a modern conservation survey of African elephants, it allowed determining the sex for over 99% of fecal samples. In a paleogenetic analysis of woolly mammoths, it produced a robust hypothesis of the sex for over 65% of the specimens out of three PCR replicates. This simple, rapid, and cost-effective procedure makes it readily applicable to large sample sizes.Laetitia Aznar-CormanoJulie BonnaldSabrina KriefNelson GumaRégis DebruyneNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Laetitia Aznar-Cormano
Julie Bonnald
Sabrina Krief
Nelson Guma
Régis Debruyne
Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
description Abstract It is important to determine the sex of elephants from their samples—faeces from the field or seized ivory—for forensic reasons or to understand population demography and genetic structure. Molecular sexing methods developed in the last two decades have often shown limited efficiency, particularly in terms of sensitivity and specificity, due to the degradation of DNA in these samples. These limitations have also prevented their use with ancient DNA samples of elephants or mammoths. Here we propose a novel TaqMan-MGB qPCR assay to address these difficulties. We designed it specifically to allow the characterization of the genetic sex for highly degraded samples of all elephantine taxa (elephants and mammoths). In vitro experiments demonstrated a high level of sensitivity and low contamination risks. We applied this assay in two actual case studies where it consistently recovered the right genotype for specimens of known sex a priori. In the context of a modern conservation survey of African elephants, it allowed determining the sex for over 99% of fecal samples. In a paleogenetic analysis of woolly mammoths, it produced a robust hypothesis of the sex for over 65% of the specimens out of three PCR replicates. This simple, rapid, and cost-effective procedure makes it readily applicable to large sample sizes.
format article
author Laetitia Aznar-Cormano
Julie Bonnald
Sabrina Krief
Nelson Guma
Régis Debruyne
author_facet Laetitia Aznar-Cormano
Julie Bonnald
Sabrina Krief
Nelson Guma
Régis Debruyne
author_sort Laetitia Aznar-Cormano
title Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
title_short Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
title_full Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
title_fullStr Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
title_full_unstemmed Molecular sexing of degraded DNA from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
title_sort molecular sexing of degraded dna from elephants and mammoths: a genotyping assay relevant both to conservation biology and to paleogenetics
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/687b8b286b4a4b7382928099b6413295
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