TY - JOUR
T1 - Density separation of petrous bone powders for optimized ancient DNA yields
AU - Fernandes, Daniel Magalhaes
AU - Sirak, Kendra A
AU - Cheronet, Olivia
AU - Novak, Mario
AU - Brück, Florian
AU - Zelger, Evelyn
AU - Llanos-Lizcano, Alejandro
AU - Wagner, Anna
AU - Zettl, Anna
AU - Mandl, Kirsten
AU - Duffett Carlson, Kellie Sara
AU - Oberreiter, Victoria
AU - Özdoğan, Kadir T
AU - Sawyer, Susanna
AU - La Pastina, Francesco
AU - Borgia, Emanuela
AU - Coppa, Alfredo
AU - Dobeš, Miroslav
AU - Velemínský, Petr
AU - Reich, David E
AU - Bell, Lynne S
AU - Pinhasi, Ron
N1 - Publisher Copyright:
© 2023 Cold Spring Harbor Laboratory Press. All rights reserved.
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85159733750&partnerID=8YFLogxK
U2 - 10.1101/gr.277714.123
DO - 10.1101/gr.277714.123
M3 - Article
C2 - 37072186
SN - 1088-9051
VL - 33
SP - 622
EP - 631
JO - Genome Research
JF - Genome Research
IS - 4
ER -