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Density separation of petrous bone powders for optimized ancient DNA yields

Genome Research 2023 6 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 40 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Daniel Fernandes, Kendra Sirak, Olivia Cheronet, Mario Novak, Florian Brück, Florian Brück, Evelyn Zelger, Evelyn Zelger, Alejandro Llanos-Lizcano, A. Wagner, Anna Zettl, Kirsten Mandl, Kellie Sara Duffet Carlson, Kellie Sara Duffet Carlson, Victoria Oberreiter, Kadir Toykan Özdoğan, Susanna Sawyer, Francesco La Pastina, Francesco La Pastina, Emanuela Borgia, Alfredo Coppa, Miroslav Dobeš, Petr Velemínský, David Reich, Lynne Bell, Ron Pinhasi

Summary

Researchers developed a density separation technique for petrous bone powders to optimize ancient DNA extraction yields, improving the recovery of genetic material from archaeological remains. The method enhances the ability to study historical populations and evolutionary questions through ancient genomics.

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/cm<sup>3</sup>, in 0.05 increments). We found that the 2.30 to 2.35 g/cm<sup>3</sup> and 2.35 to 2.40 g/cm<sup>3</sup> 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/cm<sup>3</sup> intervals may maximally optimize yields, a single separation to remove materials with a density above 2.40 g/cm<sup>3</sup> 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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