Journal
GENETICS
Volume 220, Issue 2, Pages -Publisher
GENETICS SOCIETY AMERICA
DOI: 10.1093/genetics/iyab212
Keywords
recombination; meiosis; recombination hotspot; plasticity; evolution; Prdm9
Categories
Funding
- National Institutes of Health [GM081766]
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The molecular basis for the effects of environmental conditions and speciation on meiotic recombination has been revealed through analysis of DNA sequence-dependent recombination hotspots in the fission yeast Schizosaccharomyces pombe. Changing environmental conditions directly affect local rates of recombination through DNA site-dependent hotspots, which are controlled by environmental condition-responsive signal transduction networks. Different classes of hotspots independently modulate recombination rates and can range from being inactive to highly active in response to changing conditions. This provides a molecular mechanism for the dynamic changes in the global frequency distribution of meiotic recombination.
It has long been known (circa 1917) that environmental conditions, as well as speciation, can affect dramatically the frequency distribution of Spo11/Rec12-dependent meiotic recombination. Here, by analyzing DNA sequence-dependent meiotic recombination hotspots in the fission yeast Schizosaccharomyces pombe, we reveal a molecular basis for these phenomena. The impacts of changing environmental conditions (temperature, nutrients, and osmolarity) on local rates of recombination are mediated directly by DNA site-dependent hotspots (M26, CCAAT, and Oligo-C). This control is exerted through environmental condition-responsive signal transduction networks (involving Atf1, Pcr1, Php2, Php3, Php5, and Rst2). Strikingly, individual hotspots modulate rates of recombination over a very broad dynamic range in response to changing conditions. They can range from being quiescent to being highly proficient at promoting activity of the basal recombination machinery (Spo11/Rec12 complex). Moreover, each different class of hotspot functions as an independently controlled rheostat; a condition that increases the activity of one class can decrease the activity of another class. Together, the independent modulation of recombination rates by each different class of DNA site-dependent hotspots (of which there are many) provides a molecular mechanism for highly dynamic, large-scale changes in the global frequency distribution of meiotic recombination. Because hotspot-activating DNA sites discovered in fission yeast are conserved functionally in other species, this process can also explain the previously enigmatic, Prdm9-independent, evolutionarily rapid changes in hotspot usage between closely related species, subspecies, and isolated populations of the same species.
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