Epigenetic control of pheromone MAPK signaling determines sexual fecundity in .

Several pathogenic species are capable of heritable and reversible switching between two epigenetic states, "white" and "opaque." In , white cells are essentially sterile, whereas opaque cells are mating-proficient. Here, we interrogate the mechanism by which the white-opaque switch regulates sexual fecundity and identify four genes in the pheromone MAPK pathway that are expressed at significantly higher levels in opaque cells than in white cells. These genes encode the β subunit of the G-protein complex (), the pheromone MAPK scaffold (), and the two terminal MAP kinases (). To define the contribution of each factor to mating, white cells were reverse-engineered to express elevated, opaque-like levels of these factors, either singly or in combination. We show that white cells co-overexpressing , , and undergo mating four orders of magnitude more efficiently than control white cells and at a frequency approaching that of opaque cells. Moreover, engineered white cells recapitulate the transcriptional and morphological responses of opaque cells to pheromone. These results therefore reveal multiple bottlenecks in pheromone MAPK signaling in white cells and that alleviation of these bottlenecks enables efficient mating by these "sterile" cell types. Taken together, our findings establish that differential expression of several MAPK factors underlies the epigenetic control of mating in We also discuss how fitness advantages could have driven the evolution of a toggle switch to regulate sexual reproduction in pathogenic species.