4.7 Article

Assessing the impact of USER-treatment on hyRAD capture applied to ancient DNA

期刊

MOLECULAR ECOLOGY RESOURCES
卷 22, 期 6, 页码 2262-2274

出版社

WILEY
DOI: 10.1111/1755-0998.13619

关键词

ancient DNA; DNA capture; DNA damage; DNA methylation; equids; reference bias

资金

  1. University Paul Sabatier IDEX Chaire d'Excellence (OURASI)
  2. CNRS Programme de Recherche Conjoint (PRC)
  3. CNRS International Research Project (IRP AMADEUS)
  4. European Union's Horizon 2020 Research and Innovation Programme [681605]
  5. Marie Sklodowska-Curie [797449]
  6. European Research Council (ERC)
  7. Marie Curie Actions (MSCA) [797449] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Preservation of ancient DNA in subfossil specimens allows retrieval of genetic information from the past. Capture techniques are used to economically retrieve sequence data, while USER treatment reduces sequence errors. This study shows that USER treatment can negatively impact capture efficacy and introduce experimental bias.
Ancient DNA preservation in subfossil specimens provides a unique opportunity to retrieve genetic information from the past. As ancient DNA extracts are generally dominated by molecules originating from environmental microbes, capture techniques are often used to economically retrieve orthologous sequence data at the population scale. Post-mortem DNA damage, especially the deamination of cytosine residues into uracils, also considerably inflates sequence error rates unless ancient DNA extracts are treated with the USER enzymatic mix prior to library construction. While both approaches have recently gained popularity in ancient DNA research, the impact of USER-treatment on capture efficacy still remains untested. In this study, we applied hyRAD capture to eight ancient equine subfossil specimens from France (1st-17th century CE), including horses, donkeys and their first-generation mule hybrids. We found that USER-treatment could reduce capture efficacy and introduce significant experimental bias. It differentially affected the size distribution of on-target templates following capture with two distinct hyRAD probe sets in a manner that was not driven by differences in probe sizes and DNA methylation levels. Finally, we recovered unbalanced proportions of donkey-specific and horse-specific alleles in mule capture sequence data, due to the combined effects of USER-treatment, probe sets and reference bias. Our work demonstrates that while USER-treatment can improve the quality of ancient DNA sequence data, it can also significantly affect hyRAD capture outcomes, introducing bias in the sequence data that is difficult to predict based on simple molecular probe features. Such technical batch effects may prove easier to model and correct for using capture with synthetic probes of controlled sizes and diversity content.

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