Abstract
In order to study the effect of the recombination system on protoplast fusion, intraspecific fusions were carried out using strains of Saccharomyces cerevisiae showing a wild type recombination phenotype and S. cerevisiae rem 1–2 or rad52–1 mutants. Compared with the wild type X wild type fusion, the protoplast fusion frequencies decreased dramatically when a rem1–2 mutant was used as fusion partner and increased when a rad52–1 mutant was used. The rad52–1 mutants transformed with a plasmid carrying the intact RAD52 gene showed the same fusion frequency as the wild type strains. These results strongly suggest that recombination plays a negative role during protoplast fusion.