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« Previous AbstractDedicated transporters for peptide export and intercompartmental traffic in the yeast Saccharomyces cerevisiae    Next AbstractNoninvasive Detection of Bacterial Infection in Children Using Piezoelectric E-Nose »

J Cell Biol


Title:The a-factor transporter (STE6 gene product) and cell polarity in the yeast Saccharomyces cerevisiae
Author(s):Kuchler K; Dohlman HG; Thorner J;
Address:"Department of Molecular and Cell Biology, University of California, Berkeley 94720"
Journal Title:J Cell Biol
Year:1993
Volume:120
Issue:5
Page Number:1203 - 1215
DOI: 10.1083/jcb.120.5.1203
ISSN/ISBN:0021-9525 (Print) 1540-8140 (Electronic) 0021-9525 (Linking)
Abstract:"STE6 gene product is required for secretion of the lipopeptide mating pheromone a-factor by Saccharomyces cerevisiae MATa cells. Radiolabeling and immunoprecipitation, either with specific polyclonal antibodies raised against a TrpE-Ste6 fusion protein or with mAbs that recognize c-myc epitopes in fully functional epitope-tagged Ste6 derivatives, demonstrated that Ste6 is a 145-kD phosphoprotein. Subcellular fractionation, various extraction procedures, and immunoblotting showed that Ste6 is an intrinsic plasma membrane-associated protein. The apparent molecular weight of Ste6 was unaffected by tunicamycin treatment, and the radiolabeled protein did not bind to concanavalin A, indicating that Ste6 is not glycosylated and that glycosylation is not required either for its membrane delivery or its function. The amino acid sequence of Ste6 predicts two ATP-binding folds; correspondingly, Ste6 was photoaffinity-labeled specifically with 8-azido-[alpha-32P]ATP. Indirect immunofluorescence revealed that in exponentially growing MATa cells, the majority of Ste6 showed a patchy distribution within the plasma membrane, but a significant fraction was found concentrated in a number of vesicle-like bodies subtending the plasma membrane. In contrast, in MATa cells exposed to the mating pheromone alpha-factor, which markedly induced Ste6 production, the majority of Ste6 was incorporated into the plasma membrane within the growing tip of the elongating cells. The highly localized insertion of this transporter may establish pronounced anisotropy in a-factor secretion from the MATa cell, and thereby may contribute to the establishment of the cell polarity which restricts partner selection and cell fusion during mating to one MAT alpha cell"
Keywords:"*ATP-Binding Cassette Transporters Adenosine Triphosphate/metabolism Amino Acid Sequence Biological Transport Cell Membrane/metabolism/*physiology/ultrastructure *Cell Polarity Epitopes Fungal Proteins/immunology/*metabolism Gene Expression Regulation, Fu;"
Notes:"MedlineKuchler, K Dohlman, H G Thorner, J eng GM21841/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1993/03/01 J Cell Biol. 1993 Mar; 120(5):1203-15. doi: 10.1083/jcb.120.5.1203"

 
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