A population genomics approach to uncover the CNVs, and their evolutionary significance, hidden in reduced-representation sequencing data sets

Mol Ecol. 2020 Dec;29(24):4749-4753. doi: 10.1111/mec.15665. Epub 2020 Oct 14.

Abstract

The importance of structural variation in adaptation and speciation is becoming increasingly evident in the literature. Among SVs, copy number variants (CNVs) are known to affect phenotypes through changes in gene expression and can potentially reduce recombination between alleles with different copy numbers. However, little is known about their abundance, distribution and frequency in natural populations. In a "From the Cover" article in this issue of Molecular Ecology, Dorant et al. (2020) present a new cost-effective approach to genotype copy number variants (CNVs) from large reduced-representation sequencing (RRS) data sets in nonmodel organisms, and thus to analyse sequence and structural variation jointly. They show that in American lobsters (Homarus americanus), CNVs exhibit strong population structure and several significant associations with annual variance in sea surface temperature, while SNPs fail to uncover any population structure or genotype-environment associations. Their results clearly illustrate that structural variants like CNVs can potentially store important information on differentiation and adaptive differences that cannot be retrieved from the analysis of sequence variation alone. To better understand the factors affecting the evolution of CNVs and their role in adaptation and speciation, we need to compare and synthesize data from a wide variety of species with different demographic histories and genome structure. The approach developed by Dorant et al. (2020) now allows to gain crucial knowledge on CNVs in a cost-effective way, even in species with limited genomic resources.

Keywords: adaptation; copy number variants; ecological genomics; population genomics; structural variants.

Publication types

  • Comment

MeSH terms

  • DNA Copy Number Variations* / genetics
  • Genotype
  • Metagenomics*
  • Polymorphism, Single Nucleotide / genetics
  • Temperature