Abstract

Genome duplication, which results in polyploidy, is disruptive to fundamental biological processes. Genome duplications occur spontaneously in a range of taxa and problems such as sterility, aneuploidy, and gene expression aberrations are common in newly formed polyploids. In mammals, genome duplication is associated with cancer and spontaneous abortion of embryos. Nevertheless, stable polyploid species occur in both plants and animals. Understanding how natural selection enabled these species to overcome early challenges can provide important insights into the mechanisms by which core cellular functions can adapt to perturbations of the genomic environment. Arabidopsis arenosa includes stable tetraploid populations and is related to well-characterized diploids A. lyrata and A. thaliana. It thus provides a rare opportunity to leverage genomic tools to investigate the genetic basis of polyploid stabilization. We sequenced the genomes of twelve A. arenosa individuals and found signatures suggestive of recent and ongoing selective sweeps throughout the genome. Many of these are at genes implicated in genome maintenance functions, including chromosome cohesion and segregation, DNA repair, homologous recombination, transcriptional regulation, and chromatin structure. Numerous encoded proteins are predicted to interact with one another. For a critical meiosis gene, ASYNAPSIS1, we identified a non-synonymous mutation that is highly differentiated by cytotype, but present as a rare variant in diploid A. arenosa, indicating selection may have acted on standing variation already present in the diploid. Several genes we identified that are implicated in sister chromatid cohesion and segregation are homologous to genes identified in a yeast mutant screen as necessary for survival of polyploid cells, and also implicated in genome instability in human diseases including cancer. This points to commonalities across kingdoms and supports the hypothesis that selection has acted on genes controlling genome integrity in A. arenosa as an adaptive response to genome doubling.

Highlights

  • The duplication of an entire set of chromosomes is a gamechanging mutation

  • Genome duplication and the genomic instability that generally follows can cause problems with fertility and viability, and in mammals is associated with cancer and spontaneous abortion

  • We found evidence of selection in genes that control core genome maintenance processes

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Summary

Introduction

The duplication of an entire set of chromosomes is a gamechanging mutation. Whole-genome duplication (WGD) may create challenges for basic biological functions. The regulation of gene expression, chromosome segregation, chromatin structure, and the maintenance of cellular homeostasis with altered cell size may be perturbed by duplicating an entire set of chromosomes [1,2,3,4,5,6,7,8]. That WGD can be challenging to organisms across kingdoms is evidenced by observations of dysfunction in very different contexts, such as reduced fertility observed in many newly formed plant autopolyploids, and mitotic instability in polyploid cancer cells [1,5,9]. Polyploids are especially well known among plants, and occur in a diverse array of animals, including vertebrates [11]

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