Palindromic sequence artifacts generated during next generation sequencing library preparation from historic and ancient DNA.

Degradation-specific processes and variation in laboratory protocols can bias the DNA sequence composition from samples of ancient or historic origin. Here, we identify a novel artifact in sequences from historic samples of Atlantic cod (Gadus morhua), which forms interrupted palindromes consisting...

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Bibliographic Details
Published in:PLoS ONE
Main Authors: Bastiaan Star, Alexander J Nederbragt, Marianne H S Hansen, Morten Skage, Gregor D Gilfillan, Ian R Bradbury, Christophe Pampoulie, Nils Chr Stenseth, Kjetill S Jakobsen, Sissel Jentoft
Format: Article in Journal/Newspaper
Language:English
Published: Public Library of Science (PLoS) 2014
Subjects:
R
Q
Online Access:https://doi.org/10.1371/journal.pone.0089676
https://doaj.org/article/36d00581681348debd4ee9296b31aecb
Description
Summary:Degradation-specific processes and variation in laboratory protocols can bias the DNA sequence composition from samples of ancient or historic origin. Here, we identify a novel artifact in sequences from historic samples of Atlantic cod (Gadus morhua), which forms interrupted palindromes consisting of reverse complementary sequence at the 5' and 3'-ends of sequencing reads. The palindromic sequences themselves have specific properties - the bases at the 5'-end align well to the reference genome, whereas extensive misalignments exists among the bases at the terminal 3'-end. The terminal 3' bases are artificial extensions likely caused by the occurrence of hairpin loops in single stranded DNA (ssDNA), which can be ligated and amplified in particular library creation protocols. We propose that such hairpin loops allow the inclusion of erroneous nucleotides, specifically at the 3'-end of DNA strands, with the 5'-end of the same strand providing the template. We also find these palindromes in previously published ancient DNA (aDNA) datasets, albeit at varying and substantially lower frequencies. This artifact can negatively affect the yield of endogenous DNA in these types of samples and introduces sequence bias.