Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractDetection and characterization of volatile organic compounds from burned human and animal remains in fire debris    Next AbstractEvolution of volatile compounds and biogenic amines throughout the shelf life of marinated and salted anchovies (Engraulis encrasicolus) »

J Cell Biol


Title:The conserved Pkh-Ypk kinase cascade is required for endocytosis in yeast
Author(s):deHart AK; Schnell JD; Allen DA; Hicke L;
Address:"Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, IL 60208, USA"
Journal Title:J Cell Biol
Year:2002
Volume:20020121
Issue:2
Page Number:241 - 248
DOI: 10.1083/jcb.200107135
ISSN/ISBN:0021-9525 (Print) 1540-8140 (Electronic) 0021-9525 (Linking)
Abstract:"Internalization of activated signaling receptors by endocytosis is one way cells downregulate extracellular signals. Like many signaling receptors, the yeast alpha-factor pheromone receptor is downregulated by hyperphosphorylation, ubiquitination, and subsequent internalization and degradation in the lysosome-like vacuole. In a screen to detect proteins involved in ubiquitin-dependent receptor internalization, we identified the sphingoid base-regulated serine-threonine kinase Ypk1. Ypk1 is a homologue of the mammalian serum- and glucocorticoid-induced kinase, SGK, which can substitute for Ypk1 function in yeast. The kinase activity of Ypk1 is required for receptor endocytosis because mutations in two residues important for its catalytic activity cause a severe defect in alpha-factor internalization. Ypk1 is required for both receptor-mediated and fluid-phase endocytosis, and is not necessary for receptor phosphorylation or ubiquitination. Ypk1 itself is phosphorylated by Pkh kinases, homologues of mammalian PDK1. The threonine in Ypk1 that is phosphorylated by Pkh1 is required for efficient endocytosis, and pkh mutant cells are defective in alpha-factor internalization and fluid-phase endocytosis. These observations demonstrate that Ypk1 acts downstream of the Pkh kinases to control endocytosis by phosphorylating components of the endocytic machinery"
Keywords:"3-Phosphoinositide-Dependent Protein Kinases Cloning, Molecular Conserved Sequence *Endocytosis Evolution, Molecular Glycogen Synthase Kinase 3 Mating Factor Mutation Peptides/genetics/metabolism Phosphorylation Protein Kinases/metabolism Protein Serine-T;"
Notes:"MedlinedeHart, Amy K A Schnell, Joshua D Allen, Damian A Hicke, Linda eng R01 DK053257/DK/NIDDK NIH HHS/ R01 DK53257/DK/NIDDK NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 2002/01/25 J Cell Biol. 2002 Jan 21; 156(2):241-8. doi: 10.1083/jcb.200107135. Epub 2002 Jan 21"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 01-07-2024