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« Previous Abstract[Synthesis of manganese oxide octahedral molecular sieve and their application in catalytic oxidation of benzene]    Next AbstractSubstitutions in the pheromone-responsive Gbeta protein of Saccharomyces cerevisiae confer a defect in recovery from pheromone treatment »

Mol Gen Genet


Title:Phosphorylation of the pheromone-responsive Gbeta protein of Saccharomyces cerevisiae does not affect its mating-specific signaling function
Author(s):Li E; Cismowski MJ; Stone DE;
Address:"Laboratory for Molecular Biology, University of Illinois at Chicago, 60607, USA"
Journal Title:Mol Gen Genet
Year:1998
Volume:258
Issue:6
Page Number:608 - 618
DOI: 10.1007/s004380050774
ISSN/ISBN:0026-8925 (Print) 0026-8925 (Linking)
Abstract:"The pheromone-responsive Gbeta subunit of Saccharomyces cerevisiae (encoded by STE4) is rapidly phosphorylated at multiple sites when yeast cells are exposed to mating pheromone. It has been shown that a mutant form of Ste4 lacking residues 310-346, ste4delta310-346, cannot be phosphorylated, and that its expression leads to defects in recovery from pheromone stimulation. Based on these observations, it was proposed that phosphorylation of Ste4 is associated with an adaptive response to mating pheromone. In this study we used site-directed mutagenesis to create two phosphorylation null (Pho-) alleles of STE4: ste4-T320A/S335A and ste4-T322A/S335A. When expressed in yeast, these mutant forms of Ste4 remained unphosphorylated upon pheromone stimulation. The elimination of Ste4 phosphorylation has no discernible effect on either signaling or adaptation. In addition, disruption of the FUS3 gene, which encodes a pheromone-specific MAP kinase, leads to partial loss of pheromone-induced Ste4 phosphorylation. Two-hybrid analysis suggests that the ste4delta310-346 deletion mutant is impaired in its interaction with Gpa1, the pheromone-responsive Galpha of yeast, whereas the Ste4-T320A/S335A mutant has normal affinity for Gpa1. Taken together, these results indicate that pheromone-induced phosphorylation of Ste4 is not an adaptive mechanism, and that the adaptive defect exhibited by the 310-346 deletion mutant is likely to be due to disruption of the interaction between Ste4 and Gpa1"
Keywords:"Amino Acid Sequence Calcium-Calmodulin-Dependent Protein Kinases/genetics/physiology Fungal Proteins/genetics/physiology *GTP-Binding Protein alpha Subunits GTP-Binding Protein alpha Subunits, Gq-G11 *GTP-Binding Protein beta Subunits GTP-Binding Proteins;"
Notes:"MedlineLi, E Cismowski, M J Stone, D E eng Research Support, Non-U.S. Gov't Germany 1998/07/22 Mol Gen Genet. 1998 Jun; 258(6):608-18. doi: 10.1007/s004380050774"

 
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