1. GAC1 may encode a regulatory subunit for protein phosphatase type 1 in Saccharomyces cerevisiae.
- Author
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François JM, Thompson-Jaeger S, Skroch J, Zellenka U, Spevak W, and Tatchell K
- Subjects
- Amino Acid Sequence, Base Sequence, Chromosome Mapping, Cyclic AMP metabolism, Enzyme Activation, Glycogen metabolism, Glycogen Synthase genetics, Molecular Sequence Data, Protein Kinases metabolism, Protein Phosphatase 1, Sequence Homology, Nucleic Acid, Transcription, Genetic, Fungal Proteins genetics, Gene Expression Regulation, Glycogen Synthase metabolism, Phosphoprotein Phosphatases genetics, Saccharomyces cerevisiae genetics, Saccharomyces cerevisiae Proteins
- Abstract
Elevated dosage of the GAC1 gene from the yeast Saccharomyces cerevisiae causes hyperaccumulation of glycogen whereas a gene disruption of GAC1 results in reduced glycogen levels. Glycogen synthase is almost entirely in the active, glucose 6-phosphate-independent, form in cells with increased gene dosage of GAC1 whereas the enzyme is mostly in the inactive form in strains lacking GAC1. GAC1 encodes an 88 kDa protein that is similar to the regulatory subunit (RG1) of phosphoprotein phosphatase type 1 (PP-1) from skeletal muscle that targets PP-1 to glycogen particles. Taken together, these results suggest that GAC1 encodes a regulatory subunit of PP-1. As previously shown for glycogen phosphorylase (GPH1), GAC1 RNA accumulates concomitantly with the appearance of glycogen. A strain with a mutation in the regulatory subunit of the cAMP-dependent protein kinase (bcy1) fails to accumulate GPH1 and GAC1 RNA. These results point to coordinate regulation of enzymes involved in glycogen metabolism at the level of RNA accumulation and indicate that at least part of this control is exerted by the RAS-cAMP pathway.
- Published
- 1992
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