Mutational analysis of Cak1p, an essential protein kinase that regulates cell cycle progression.

In Saccharomyces cerevisiae, entry into S phase requires the activation of the protein kinase Cdc28p through binding with cyclin Clb5p or Clb6p, as well as the destruction of the cyclin-dependent kinase inhibitor Sic1p. Mutants that are defective in this activation event arrest after START, with unreplicated DNA and multiple, elongated ...
buds. These mutants include cells defective in CDC4, CDC34 or CDC53, as well as cells that have lost all CLB function. Here we describe mutations in another gene, CAK1, that lead to a similar arrest. Cells that are defective in CAK1 are inviable and arrest with a single nucleus and multiple, elongated buds. CAK1 encodes a protein kinase most closely related to the Cdc2p family of protein kinases. Mutations that lead to the production of an inactive kinase that can neither autophosphorylate, nor phosphorylate Cdc28p in vitro are also incapable of rescuing a cell with a deletion of CAK1. These results underscore the importance of the Cak1p protein kinase activity in cell cycle progression.
Mesh Terms:
Amino Acid Sequence, Animals, CDC28 Protein Kinase, S cerevisiae, Cell Cycle, Cyclin-Dependent Kinases, DNA Mutational Analysis, Molecular Sequence Data, Phenotype, Protein Kinases, Protein-Serine-Threonine Kinases, Rabbits, Recombinant Fusion Proteins, Saccharomyces cerevisiae
Mol. Gen. Genet.
Date: Oct. 01, 1997
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