Abstract
The CDC7 protein of Saccharomyces cerevisiae may be involved in the G1/S-phase transition and/or in the initiation of mitotic DNA synthesis. The CDC7 gene has two in-frame AUG codons as possible translation start sites, which would produce 58- and 56-kDa proteins, respectively. Both p58 and p56 derived from recombinant plasmids complement the temperature-sensitive growth defect of the cdc7-1 allele. To determine the biochemical function of the CDC7 protein, the CDC7 gene was cloned and polyclonal antibodies were produced against the CDC7 protein. CDC7 immune complexes prepared from yeast with these antibodies phosphorylate histone H1. Kinase activity is thermolabile in strains carrying the cdc7-1 temperature-sensitive mutant allele and is elevated greater than 10-fold in strains carrying plasmids overexpressing either p56 or p58, confirming that the kinase in the immunoprecipitates is the CDC7 gene product. In addition, we show that CDC7 is a phosphoprotein itself. Indirect immunofluorescence and biochemical fractionation show that the CDC7 protein is present at relatively high concentrations in the nucleus compared with the cytoplasm, suggesting that nuclear proteins may be substrates for the CDC7 protein.
MeSH Terms
Cell Cycle
Cell Cycle Proteins
Cell Nucleus/enzymology
Cloning, Molecular
Fluorescent Antibody Technique
Fungal Proteins/metabolism
Molecular Weight
Nuclear Proteins/physiology
Phosphoproteins/metabolism
Protein Kinases/metabolism,physiology
Protein Serine-Threonine Kinases
Recombinant Proteins
Saccharomyces cerevisiae/cytology,enzymology
Saccharomyces cerevisiae Proteins
Chemicals
Cell Cycle Proteins
Fungal Proteins
Nuclear Proteins
Phosphoproteins
Recombinant Proteins
Saccharomyces cerevisiae Proteins
Protein Kinases
CDC7 protein, S cerevisiae
Protein Serine-Threonine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Yoon H J
Braun Laboratories, California Institute of Technology, Pasadena 91125.
Campbell J L
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