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    The half-life of DNA in bone: measuring decay kinetics in 158 dated fossils

    Access Status
    Open access via publisher
    Authors
    Allentoft, M.
    Collins, M.
    Harker, D.
    Haile, James
    Oskam, C.
    Hale, M.
    Campos, P.
    Samaniego, J.
    Gilbert, Thomas
    Willerslev, E.
    Zhang, G.
    Scofield, R.
    Holdaway, R.
    Bunce, Michael
    Date
    2012
    Type
    Journal Article
    
    Metadata
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    Citation
    Allentoft, M. and Collins, M. and Harker, D. and Haile, J. and Oskam, C. and Hale, M. and Campos, P. et al. 2012. The half-life of DNA in bone: measuring decay kinetics in 158 dated fossils. Proceedings of the Royal Society B: Biological Sciences. 279 (1748): pp. 4724-4733.
    Source Title
    Proceedings of the Royal Society B: Biological Sciences
    DOI
    10.1098/rspb.2012.1745
    ISSN
    1471-2954
    URI
    http://hdl.handle.net/20.500.11937/19470
    Collection
    • Curtin Research Publications
    Abstract

    Claims of extreme survival of DNA have emphasized the need for reliable models of DNA degradationthrough time. By analysing mitochondrial DNA (mtDNA) from 158 radiocarbon-dated bones of theextinct New Zealand moa, we confirm empirically a long-hypothesized exponential decay relationship.The average DNA half-life within this geographically constrained fossil assemblage was estimated to be521 years for a 242 bp mtDNA sequence, corresponding to a per nucleotide fragmentation rate (k) of5.50 ! 10–6 per year. With an effective burial temperature of 13.18C, the rate is almost 400 timesslower than predicted from published kinetic data of in vitro DNA depurination at pH 5. Althoughbest described by an exponential model (R2 ¼ 0.39), considerable sample-to-sample variance in DNApreservation could not be accounted for by geologic age. This variation likely derives from differencesin taphonomy and bone diagenesis, which have confounded previous, less spatially constrained attempt to study DNA decay kinetics. Lastly, by calculating DNA fragmentation rates on Illumina HiSeq data, we show that nuclear DNA has degraded at least twice as fast as mtDNA. These results provide a baseline for predicting long-term DNA survival in bone.

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