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« Previous AbstractIdentification and characterization of a mutation affecting the division arrest signaling of the pheromone response pathway in Saccharomyces cerevisiae    Next AbstractMolecular monitoring of the transcriptional activation of the yeast Saccharomyces kluyveri mating pheromone signal transduction by using FUS1-lacZ fusion gene »

Curr Genet


Title:Molecular cloning of the DAC2/FUS3 gene essential for pheromone-induced G1-arrest of the cell cycle in Saccharomyces cerevisiae
Author(s):Fujimura H;
Address:"Laboratory for Molecular Biology, Hoechst Japan Ltd., Kawagoe, Japan"
Journal Title:Curr Genet
Year:1990
Volume:18
Issue:5
Page Number:395 - 400
DOI: 10.1007/BF00309907
ISSN/ISBN:0172-8083 (Print) 0172-8083 (Linking)
Abstract:"Mating pheromones, known as a and alpha-factors, arrest the division of cells of opposite mating types, alpha and a respectively, in Saccharomyces cerevisiae. I have cloned the DAC2 gene, which is required for both pheromone-induced division-arrest and cell-fusion during conjugation. The constructed dac2::LEU2 null mutation leads to defects in both pheromone-induced division-arrest and cell-fusion during conjugation; it also suppresses the growth defect caused by the gpa1 mutation (a mutation in the alpha subunit of the S. cerevisiae G protein). These results indicate that DAC2 may be the same gene as FUS3, which was recently isolated by Elion et al. (1990) as a gene essential for cell-fusion during conjugation. The dac2::LEU2 null mutant also showed morphological alterations in response to mating pheromones. I show here that the DAC2 product plays an essential role in both the division-arrest signalling pathway of the yeast pheromone response and in cell-fusion during conjugation"
Keywords:"Cloning, Molecular G1 Phase Genes, Fungal Mating Factor Mutation Peptides/*pharmacology Phenotype Pheromones/*pharmacology Restriction Mapping Saccharomyces cerevisiae/cytology/*genetics Signal Transduction Suppression, Genetic;"
Notes:"MedlineFujimura, H eng 1990/12/01 Curr Genet. 1990 Dec; 18(5):395-400. doi: 10.1007/BF00309907"

 
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