Abstract

Ancient DNA provides an opportunity to infer the drivers of natural selection by linking allele frequency changes to temporal shifts in environment or cultural practices. However, analyses have often been hampered by uneven sampling and uncertainties in sample dating, as well as being confounded by demographic processes. Here, we present a Bayesian statistical framework for quantifying the timing and strength of selection using ancient DNA that explicitly addresses these challenges. We applied this method to time series data for two loci: TSHR and BCDO2, both hypothesised to have undergone strong and recent selection in domestic chickens. The derived variant in TSHR, associated with reduced aggression to conspecifics and faster onset of egg laying, shows strong selection beginning around 1,100 years ago, coincident with archaeological evidence for intensified chicken production and documented changes in egg and chicken consumption. To our knowledge, this is the first example of preindustrial domesticate trait selection in response to a historically attested cultural shift in food preference. For BCDO2, we find support for selection, but demonstrate that the recent rise in allele frequency could also have been driven by gene flow from imported Asian chickens during more recent breed formations. Our findings highlight that traits found ubiquitously in modern domestic species may not necessarily have originated during the early stages of domestication. In addition, our results demonstrate the importance of precise estimation of allele frequency trajectories through time for understanding the drivers of selection.

Highlights

  • To account for allelic dropout that is common in ancient DNA studies (Svensson et al 2007), each SNP/genotype was confirmed by repeated genotyping from two to eight independent PCRs

  • The 14 new samples come from three different archaeological sites located in Morocco and Turkey

  • The chicken samples newly genotyped for this study come from a third period, corresponding to a modern re-occupation, which started in the 17th/18th century and lasted into the 20th century CE

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Summary

Introduction

PCR set-up was performed in a fume hood in a dedicated facility adjacent to the dedicated ancient DNA extraction facility. BCDO2: PCRs were set up in 25-μL reactions using 1.0–1.25 U Taq GOLD (Applied Biosystems), 1× Gold buffer (Applied Bio- systems), 2.5 mM MgCl2, 0.5 μg/μL BSA, 1 M betaine, 200 μM of each dNTP, 0.4 μM of each primer, and 2–5 μL of ancient DNA extract. DNA Genotyping Pyrosequencing was performed in-house at the Archaeology department in Durham using the PyroMark Q24 (Qiagen) following manufacturers guidelines, and using Qiagen Q24 sequencing reagent kits.

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