Genetic interactions between REG1/HEX2 and GLC7, the gene encoding the protein phosphatase type 1 catalytic subunit in Saccharomyces cerevisiae.
Mutations in GLC7, the gene encoding the type 1 protein phosphatase catalytic subunit, cause a variety of abberrant phenotypes in yeast, such as impaired glycogen synthesis and relief of glucose repression of the expression of some genes. Loss of function of the REG1/HEX2 gene, necessary for glucose repression of several genes, was found to suppress the glycogen-deficient phenotype of the glc7-1 allele. Deletion of REG1 in a wild-type background led to overaccumulation of glycogen as well as slow growth and an enlarged cell size. However, loss of REG1 did not suppress other phenotypes associated with GLC7 mutations, such as inability to sporulate or, in cells bearing the glc7Y-170 allele, lack of growth at 14 degrees. The effect of REG1 deletion on glycogen accumulation is not simply due to derepression of glucose-repressed genes, although it does require the presence of SNF1, which encodes a protein kinase essential for expression of glucose-repressed genes and for glycogen accumulation. We propose that REG1 has a role in controlling glycogen accumulation.
Pubmed ID: 8722767 RIS Download
Base Sequence | DNA Primers | Fungal Proteins | Gene Deletion | Genes, Fungal | Genetic Complementation Test | Genotype | Glycogen | Molecular Sequence Data | Mutagenesis | Mutagenesis, Insertional | Phosphoprotein Phosphatases | Polymerase Chain Reaction | Protein Phosphatase 1 | Restriction Mapping | Saccharomyces cerevisiae | Saccharomyces cerevisiae Proteins