Chromosome-refolding model of mating-type switching in yeast

Abstract

Chromosomes are folded into cells in a nonrandom fashion, with particular genetic loci occupying distinct spatial regions. This observation raises the question of whether the spatial organization of a chromosome governs its functions, such as recombination or transcription. We consider this general question in the specific context of mating-type switching in budding yeast, which is a model system for homologous recombination. Mating-type switching is induced by a DNA double-strand break (DSB) at theMATlocus on chromosome III, followed by homologous recombination between the cutMATlocus and one of two donor loci (HMLα andHMRa), located on the same chromosome. Previous studies have suggested that inMATa cells after the DSB is induced chromosome III undergoes refolding, which directs theMATlocus to recombine withHMLα. Here, we propose a quantitative model of mating-type switching predicated on the assumption of DSB-induced chromosome refolding, which also takes into account the previously measured stochastic dynamics and polymer nature of yeast chromosomes. Using quantitative fluorescence microscopy, we measure changes in the distance between the donor (HMLα) andMATloci after the DSB and find agreement with the theory. Predictions of the theory also agree with measurements of changes in the use ofHMLα as the donor, when we perturb the refolding of chromosome III. These results establish refolding of yeast chromosome III as a key driving force inMATswitching and provide an example of a cell regulating the spatial organization of its chromosome so as to direct homology search during recombination.