Title: | Metabolism of alpha-factor by a mating type cells of Saccharomyces cerevisiae |
Author(s): | Finkelstein DB; Strausberg S; |
ISSN/ISBN: | 0021-9258 (Print) 0021-9258 (Linking) |
Abstract: | "When a mating type cells of Saccharomyces cerevisiae are exposed to the mating pheromone alpha-factor in liquid cultures, there is a time-dependent loss of alpha-factor activity from the culture fluid. This loss of biological activity can be directly correlated with the proteolysis of the pheromone by a mating type cells. The metabolism of alpha-factor by a mating type cells may be measured by using either in vitro 125I-labeled or in vivo 35S-labeled pheromone. Addition of chloroquine to growing cultures of a mating type cells at concentrations which cause no detectable alterations in cell growth produces a potentiation of alpha-factor mediated cell cycle arrest. This potentiation of alpha-factor activity is directly correlated with the inhibition of alpha-factor proteolysis. Thus, while proteolytic digestion of alpha-factor appears to be related to the mechanism whereby a mating type cells 'detoxify' alpha-factor and recover from cell cycle arrest, proteolysis of the mating factor is not necessary for alpha-factor mediated cell cycle arrest" |
Keywords: | "Chloroquine/pharmacology Genetics, Microbial Kinetics Pepsin A Peptides/*metabolism Saccharomyces cerevisiae/metabolism/*physiology Sulfuric Acids/metabolism;" |
Notes: | "MedlineFinkelstein, D B Strausberg, S eng Research Support, U.S. Gov't, Non-P.H.S. 1979/02/10 J Biol Chem. 1979 Feb 10; 254(3):796-803" |