4.8 Article

Genome Duplication Increases Meiotic Recombination Frequency: A Saccharomyces cerevisiae Model

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 38, Issue 3, Pages 777-787

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msaa219

Keywords

meiotic recombination frequency; genome duplication; tetrasomic linkage analysis; S. cerevisiae

Funding

  1. National Nature Science Foundation [31671328, 31871240, 91231114]
  2. State Key project of China [2016YFC1305501]
  3. BBSRC [BB/N008952/1]
  4. Leverhulme Trust in the United Kingdom
  5. BBSRC [BB/N008952/1] Funding Source: UKRI

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Genetic recombination is a vital process in meiosis, contributing to genome stability and genetic variation for natural and artificial selection, and is influenced by various biological and abiotic factors. Genome polyploidization leads to a significant increase in meiotic recombination frequency, accompanied by other biological changes.
Genetic recombination characterized by reciprocal exchange of genes on paired homologous chromosomes is the most prominent event in meiosis of almost all sexually reproductive organisms. It contributes to genome stability by ensuring the balanced segregation of paired homologs in meiosis, and it is also the major driving factor in generating genetic variation for natural and artificial selection. Meiotic recombination is subjected to the control of a highly stringent and complex regulating process and meiotic recombination frequency (MRF) may be affected by biological and abiotic factors such as sex, gene density, nucleotide content, and chemical/temperature treatments, having motivated tremendous researches for artificially manipulating MRF. Whether genome polyploidization would lead to a significant change in MRF has attracted both historical and recent research interests; however, tackling this fundamental question is methodologically challenging due to the lack of appropriate methods for tetrasomic genetic analysis, thus has led to controversial conclusions in the literature. This article presents a comprehensive and rigorous survey of genome duplication-mediated change in MRF using Saccharomyces cerevisiae as a eukaryotic model. It demonstrates that genome duplication can lead to consistently significant increase in MRF and rate of crossovers across all 16 chromosomes of S. cerevisiae, including both cold and hot spots of MRF. This ploidy-driven change in MRF is associated with weakened recombination interference, enhanced double-strand break density, and loosened chromatin histone occupation. The study illuminates a significant evolutionary feature of genome duplication and opens an opportunity to accelerate response to artificial and natural selection through polyploidization.

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