The genetic architecture of temperature adaptation is shaped by population ancestry and not by selection regime

Genome Biol. 2021 Jul 16;22(1):211. doi: 10.1186/s13059-021-02425-9.

Abstract

Background: Understanding the genetic architecture of temperature adaptation is key for characterizing and predicting the effect of climate change on natural populations. One particularly promising approach is Evolve and Resequence, which combines advantages of experimental evolution such as time series, replicate populations, and controlled environmental conditions, with whole genome sequencing. Recent analysis of replicate populations from two different Drosophila simulans founder populations, which were adapting to the same novel hot environment, uncovered very different architectures-either many selection targets with large heterogeneity among replicates or fewer selection targets with a consistent response among replicates.

Results: Here, we expose the founder population from Portugal to a cold temperature regime. Although almost no selection targets are shared between the hot and cold selection regime, the adaptive architecture was similar. We identify a moderate number of targets under strong selection (19 selection targets, mean selection coefficient = 0.072) and parallel responses in the cold evolved replicates. This similarity across different environments indicates that the adaptive architecture depends more on the ancestry of the founder population than the specific selection regime.

Conclusions: These observations will have broad implications for the correct interpretation of the genomic responses to a changing climate in natural populations.

Keywords: Adaptive architecture; Experimental evolution; Temperature adaptation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / genetics*
  • Alleles
  • Animals
  • Cold Temperature
  • Drosophila simulans / genetics*
  • Female
  • Florida
  • Gene Frequency
  • Genetics, Population
  • Genome, Insect*
  • Genomics / methods*
  • High-Throughput Nucleotide Sequencing
  • Hot Temperature
  • Linkage Disequilibrium
  • Male
  • Multifactorial Inheritance*
  • Portugal

Associated data

  • Dryad/10.5061/dryad.np5hqbzsp