Density separation of petrous bone powders for optimized ancient DNA yields
Fernandes DMPapers in this archive, Sirak KAPapers in this archive, Cheronet OPapers in this archive, Novak MPapers in this archive, Brück FPapers in this archive, Zelger EPapers in this archive, Llanos-Lizcano APapers in this archive, Wagner APapers in this archive, Zettl APapers in this archive, Mandl KPapers in this archive, Duffet Carlson KSPapers in this archive, Oberreiter VPapers in this archive, Özdoğan KTPapers in this archive, Sawyer SPapers in this archive, La Pastina FPapers in this archive, Borgia EPapers in this archive, Coppa APapers in this archive, Dobeš MPapers in this archive, Velemínský PPapers in this archive, Reich DPapers in this archive, Bell LSPapers in this archive, Pinhasi RPapers in this archive
Abstract
Density separation is a process routinely used to segregate minerals, organic matter, and even microplastics, from soils and sediments. Here we apply density separation to archaeological bone powders before DNA extraction to increase endogenous DNA recovery relative to a standard control extraction of the same powders. Using nontoxic heavy liquid solutions, we separated powders from the petrous bones of 10 individuals of similar archaeological preservation into eight density intervals (2.15 to 2.45 g/cm3, in 0.05 increments). We found that the 2.30 to 2.35 g/cm3 and 2.35 to 2.40 g/cm3 intervals yielded up to 5.28-fold more endogenous unique DNA than the corresponding standard extraction (and up to 8.53-fold before duplicate read removal), while maintaining signals of ancient DNA authenticity and not reducing library complexity. Although small 0.05 g/cm3 intervals may maximally optimize yields, a single separation to remove materials with a density above 2.40 g/cm3 yielded up to 2.57-fold more endogenous DNA on average, which enables the simultaneous separation of samples that vary in preservation or in the type of material analyzed. While requiring no new ancient DNA laboratory equipment and fewer than 30 min of extra laboratory work, the implementation of density separation before DNA extraction can substantially boost endogenous DNA yields without decreasing library complexity. Although subsequent studies are required, we present theoretical and practical foundations that may prove useful when applied to other ancient DNA substrates such as teeth, other bones, and sediments.
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