Sex chromosomes often show extensive areas of suppressed recombination and cytological differentiation, a well-documented phenomenon in animals and plants. Lack of recombination is expected to limit the efficacy of natural selection, leading to degeneration in gene content. Similarly, fungal mating-type chromosomes can display patterns of suppressed recombination, however the mechanisms responsible and the extent of genic degeneration are still unclear. The proposed research investigates the evolution of fungal mating-type chromosomes, more specifically the patterns and mechanisms underlying genomic regions with suppressed recombination linked to mating compatibility genes and how this phenomenon impacts fitness and the genome. I use comparative genomics and a model fungal system with dimorphic mating-type chromosomes of different degrees and ages for understanding the steps involved in the evolution of suppressed recombination and genomic degeneration. This project compiles results that yield unprecedented insights into the evolution of mating-type chromosomes, the dynamics of genome degradation in sexual eukaryotic species, and more generally contribute for a unified view of evolution in dimorphic chromosomes with suppressed recombination.