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      Successful enrichment and recovery of whole mitochondrial genomes from ancient human dental calculus

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          ABSTRACT

          Objectives

          Archaeological dental calculus is a rich source of host‐associated biomolecules. Importantly, however, dental calculus is more accurately described as a calcified microbial biofilm than a host tissue. As such, concerns regarding destructive analysis of human remains may not apply as strongly to dental calculus, opening the possibility of obtaining human health and ancestry information from dental calculus in cases where destructive analysis of conventional skeletal remains is not permitted. Here we investigate the preservation of human mitochondrial DNA (mtDNA) in archaeological dental calculus and its potential for full mitochondrial genome (mitogenome) reconstruction in maternal lineage ancestry analysis.

          Materials and Methods

          Extracted DNA from six individuals at the 700‐year‐old Norris Farms #36 cemetery in Illinois was enriched for mtDNA using in‐solution capture techniques, followed by Illumina high‐throughput sequencing.

          Results

          Full mitogenomes (7–34×) were successfully reconstructed from dental calculus for all six individuals, including three individuals who had previously tested negative for DNA preservation in bone using conventional PCR techniques. Mitochondrial haplogroup assignments were consistent with previously published findings, and additional comparative analysis of paired dental calculus and dentine from two individuals yielded equivalent haplotype results. All dental calculus samples exhibited damage patterns consistent with ancient DNA, and mitochondrial sequences were estimated to be 92–100% endogenous. DNA polymerase choice was found to impact error rates in downstream sequence analysis, but these effects can be mitigated by greater sequencing depth.

          Discussion

          Dental calculus is a viable alternative source of human DNA that can be used to reconstruct full mitogenomes from archaeological remains. Am J Phys Anthropol 160:220–228, 2016. © 2016 The Authors American Journal of Physical Anthropology Published by Wiley Periodicals, Inc.

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          Most cited references30

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          Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platform

          Due to the increasing throughput of current DNA sequencing instruments, sample multiplexing is necessary for making economical use of available sequencing capacities. A widely used multiplexing strategy for the Illumina Genome Analyzer utilizes sample-specific indexes, which are embedded in one of the library adapters. However, this and similar multiplex approaches come with a risk of sample misidentification. By introducing indexes into both library adapters (double indexing), we have developed a method that reveals the rate of sample misidentification within current multiplex sequencing experiments. With ~0.3% these rates are orders of magnitude higher than expected and may severely confound applications in cancer genomics and other fields requiring accurate detection of rare variants. We identified the occurrence of mixed clusters on the flow as the predominant source of error. The accuracy of sample identification is further impaired if indexed oligonucleotides are cross-contaminated or if indexed libraries are amplified in bulk. Double-indexing eliminates these problems and increases both the scope and accuracy of multiplex sequencing on the Illumina platform.
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            Patterns of damage in genomic DNA sequences from a Neandertal.

            High-throughput direct sequencing techniques have recently opened the possibility to sequence genomes from Pleistocene organisms. Here we analyze DNA sequences determined from a Neandertal, a mammoth, and a cave bear. We show that purines are overrepresented at positions adjacent to the breaks in the ancient DNA, suggesting that depurination has contributed to its degradation. We furthermore show that substitutions resulting from miscoding cytosine residues are vastly overrepresented in the DNA sequences and drastically clustered in the ends of the molecules, whereas other substitutions are rare. We present a model where the observed substitution patterns are used to estimate the rate of deamination of cytosine residues in single- and double-stranded portions of the DNA, the length of single-stranded ends, and the frequency of nicks. The results suggest that reliable genome sequences can be obtained from Pleistocene organisms.
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              A revised timescale for human evolution based on ancient mitochondrial genomes.

              Recent analyses of de novo DNA mutations in modern humans have suggested a nuclear substitution rate that is approximately half that of previous estimates based on fossil calibration. This result has led to suggestions that major events in human evolution occurred far earlier than previously thought. Here, we use mitochondrial genome sequences from ten securely dated ancient modern humans spanning 40,000 years as calibration points for the mitochondrial clock, thus yielding a direct estimate of the mitochondrial substitution rate. Our clock yields mitochondrial divergence times that are in agreement with earlier estimates based on calibration points derived from either fossils or archaeological material. In particular, our results imply a separation of non-Africans from the most closely related sub-Saharan African mitochondrial DNAs (haplogroup L3) that occurred less than 62-95 kya. Though single loci like mitochondrial DNA (mtDNA) can only provide biased estimates of population divergence times, they can provide valid upper bounds. Our results exclude most of the older dates for African and non-African population divergences recently suggested by de novo mutation rate estimates in the nuclear genome. Copyright © 2013 Elsevier Ltd. All rights reserved.
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                Author and article information

                Journal
                Am J Phys Anthropol
                Am. J. Phys. Anthropol
                10.1002/(ISSN)1096-8644
                AJPA
                American Journal of Physical Anthropology
                John Wiley and Sons Inc. (Hoboken )
                0002-9483
                1096-8644
                16 March 2016
                June 2016
                : 160
                : 2 ( doiID: 10.1002/ajpa.v160.2 )
                : 220-228
                Affiliations
                [ 1 ] Department of AnthropologyUniversity of Oklahoma Norman OK 73019
                [ 2 ] School of Human Evolution and Social ChangeArizona State University Tempe AZ 85287
                [ 3 ] School of Life SciencesArizona State University Tempe AZ 85287
                [ 4 ] Department of AnthropologyPennsylvania State University, University Park PA 16802
                [ 5 ]Center for Bioarchaeological Research, Arizona State University Tempe AZ 85287
                [ 6 ]Institute of Human Origins, Arizona State University Tempe AZ 85287
                [ 7 ]Institute of Evolutionary Medicine, University of Zurich 8057 ZurichSwitzerland
                Author notes
                [*] [* ]Correspondence to: Christina Warinner, Department of Anthropology, 101 David L. Boren Blvd. Norman, OK 73019. E‐mail: twarinner@ 123456gmail.com
                Article
                AJPA22960
                10.1002/ajpa.22960
                4866892
                26989998
                4a5c6698-2a6c-48a6-babc-d0d8ffd5ddc6
                © 2016 The Authors American Journal of Physical Anthropology Published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 September 2015
                : 05 January 2016
                : 25 January 2016
                Page count
                Pages: 9
                Funding
                Funded by: National Science Foundation
                Award ID: BCS‐1063939; BCS‐1515163
                Award ID: BCS‐1516633
                Funded by: National Institutes of Health
                Award ID: R01 GM‐089866
                Funded by: Illinois State Museum
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                ajpa22960
                June 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:13.09.2016

                Anthropology
                ancient dna,dental calculus,mitogenome,mitochondrial genome,next‐generation sequencing,in‐solution capture enrichment,nagpra,ethics,mississippian culture

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