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      First complete mitochondrial genome data from ancient South American camelids - The mystery of the chilihueques from Isla Mocha (Chile)

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          Abstract

          In South American societies, domesticated camelids were of great cultural importance and subject to trade and translocation. South American camelids were even found on remote and hard to reach islands, emphasizing their importance to historic and pre-historic South American populations. Isla Mocha, a volcanic island 35 km offshore of Central-South Chile, is an example of such an island. When Dutch and Spanish explorers reached the island in the early 17th century, they found that domesticated camelids called “ chilihueque” played a major role in the island’s society. The origin and taxonomy of these enigmatic camelids is unclear and controversial. This study aims to resolve this controversy through genetic analyses of Isla Mocha camelid remains dating from pre-Columbian to early historic times. A recent archaeological excavation of site P21-3 on Isla Mocha yielded a number of camelid remains. Three complete mitochondrial genomes were successfully recovered and analysed. Phylogenetic analyses suggest that “ chilihueque” was a local term for a domesticated guanaco. Results from phylogeographic analyses are consistent with Isla Mocha camelids being sourced from Southern Chilean guanaco populations. Our data highlights the capability of ancient DNA to answer questions about extinct populations which includes species identity, potential translocation events and origins of founding individuals.

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          Ancient DNA extraction from bones and teeth.

          This method is designed to maximize recovery of PCR-amplifiable DNA from ancient bone and teeth specimens and at the same time to minimize co-extraction of substances that inhibit PCR. This is achieved by a combination of DNA extraction from bone powder using a buffer consisting solely of EDTA and proteinase K, and purification of the DNA by binding to silica in the presence of high concentrations of guanidinium thiocyanate. All steps are performed at room temperature (20-23 degrees C), thereby reducing further degradation of the already damaged and fragile ancient DNA and providing an optimal trade-off between DNA release and degradation. Furthermore, the purification step removes most of the various types of PCR inhibitors present in ancient bone samples, thereby optimizing the amount of ancient DNA available for subsequent enzymatic manipulation, such as PCR amplification. The protocol presented here allows DNA extraction from ancient bone and teeth with a minimum of working steps and equipment and yields DNA extracts within 2 working days.
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            Author and article information

            Journal
            Sci Rep
            Sci Rep
            Scientific Reports
            Nature Publishing Group
            2045-2322
            08 December 2016
            2016
            : 6
            : 38708
            Affiliations
            [1 ]Department of Mathematics and Natural Sciences, Evolutionary and Adaptive Genomics, Institute for Biochemistry and Biology, University of Potsdam , Karl-Liebknecht-Str. 24-25, 14476 Potsdam, Germany
            [2 ]Department of Integrative Biology, University of California Berkeley , 3040 Valley Life Sciences Building, Berkeley, CA 94720-3140, USA
            [3 ]Department of Biology, Stanford University , 371 Serra Street, Palo Alto, CA 94305-5020, USA
            [4 ]School of Anthropology, Faculty of Social Sciences, Universidad Academia de Humanismo Cristiano , Condell 506, Santiago 7500828, Chile
            [5 ]Centro de Estudios Avanzados, Universidad de Playa Ancha , Traslaviña 450, Viña del Mar, Chile
            [6 ]Department of Anatomy, University of Otago , 270 Great King Street, Dunedin 9016, New Zealand
            Author notes
            Article
            srep38708
            10.1038/srep38708
            5144146
            27929050
            f531704b-f38f-41af-a721-0ef74489d862
            Copyright © 2016, The Author(s)

            This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

            History
            : 27 July 2016
            : 10 November 2016
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