Genetic and Biochemical Analysis of the Yeast Plasma Membrane Ssy1p-Ptr3p-Ssy5p Sensor of Extracellular Amino Acids
- 1 February 2001
- journal article
- research article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 21 (3) , 814-826
- https://doi.org/10.1128/mcb.21.3.814-826.2001
Abstract
Ssy1p and Ptr3p are known components of a yeast plasma membrane system that functions to sense the presence of amino acids in the extracellular environment. In response to amino acids, this sensing system initiates metabolic signals that ultimately regulate the functional expression of several amino acid-metabolizing enzymes and transport proteins, including multiple, genetically distinct amino acid permeases. We have found that SSY5 encodes a third component of this amino acid sensing system. Mutations inSSY5 manifest phenotypes that are indistinguishable from those resulting from either single ssy1 andptr3 mutations or ssy5 ssy1 and ssy5 ptr3 double mutations. Although Ssy5p is predicted to be a soluble protein, it exhibits properties indicating that it is a peripherally associated plasma membrane protein. Each of the three sensor components, Ssy1p, Ptr3p, and Ssy5p, adopts conformations and modifications that are dependent upon the availability of amino acids and on the presence of the other two components. These results suggest that these components function as part of a sensor complex localized to the plasma membrane. Consistent with a sensor complex, the overexpression of SSY1 or the unique N-terminal extension of this amino acid permease homologue inactivates the amino acid sensor in a dominant-negative manner. Each of the components of the Ssy1p-Ptr3p-Ssy5p (SPS) signaling system undergoes rapid physical changes, reflected in altered electrophoretic mobility, when leucine is added to cells grown in media lacking amino acids. Furthermore, the levels of each SPS sensor component present in whole-cell extracts diminish upon leucine addition. The rapid physical alterations and reduced levels of sensor components are consistent with their being downregulated in response to amino acid availability. These results reveal the dynamic nature of the amino acid-initiated signals transduced by the SPS sensor.Keywords
This publication has 88 references indexed in Scilit:
- A Method for Determining the in VivoTopology of Yeast Polytopic Membrane Proteins Demonstrates That Gap1p Fully Integrates into the Membrane Independently of Shr3pPublished by Elsevier ,2000
- Dominant negative mutations in the α-factor receptor, a G protein-coupled receptor encoded by the STE2 gene of the yeast Saccharomyces cerevisiaeMolecular Genetics and Genomics, 1999
- Yeast Transcriptional Regulator Leu3pPublished by Elsevier ,1999
- Combinatorial control in ubiquitin-dependent proteolysis: don't Skp the F-box hypothesisTrends in Genetics, 1998
- The C-terminal domain of Snf3p mediates glucose-responsive signal transduction inSaccharomyces cerevisiaeFEMS Microbiology Letters, 1998
- Two glucose transporters in Saccharomyces cerevisiae are glucose sensors that generate a signal for induction of gene expression.Proceedings of the National Academy of Sciences, 1996
- Ubiquitination Mediated by the Npi1p/Rsp5p Ubiquitin-protein Ligase Is Required for Endocytosis of the Yeast Uracil PermeaseJournal of Biological Chemistry, 1996
- Membrane targeting of the nucleotide exchange factor Sos is sufficient for activating the Ras signaling pathwayCell, 1994
- Maturation of the yeast plasma membrane [H+]ATPase involves phosphorylation during intracellular transport.The Journal of cell biology, 1991
- Non specific induction of arginase in Saccharomyces cerevisiaeBiochimie, 1976