Molecular and General Genetics MGG

, Volume 262, Issue 1, pp 55–64

The cyclin-dependent kinase inhibitory domain of the yeast Sic1 protein is contained within the C-terminal 70 amino acids

Authors

  • A. Hodge
    • L. P. Markey Cancer Center, University of Kentucky, Lexington, KY 40536-0096, USA
  • M. Mendenhall
    • L. P. Markey Cancer Center, University of Kentucky, Lexington, KY 40536-0096, USA
ORIGINAL PAPER

DOI: 10.1007/s004380051059

Cite this article as:
Hodge, A. & Mendenhall, M. Mol Gen Genet (1999) 262: 55. doi:10.1007/s004380051059

Abstract

By inhibiting the activity of Cdc28/Clb cyclin-dependent protein kinase (CDK) complexes, Sic1 prevents the premature initiation of S phase in the yeast Saccharomyces cerevisiae. By testing a series of Sic1 truncation mutants, we have mapped the minimal domain necessary for Cdc28/Clb inhibition in vivo to the C-terminal 70 amino acids of Sic1. Site-directed mutagenesis was used to show that a sequence that matches the zRxL motif found in mammalian CDK inhibitors is essential for Sic1 function. This motif is not found in the Schizosaccharomyces CDK inhibitor p25rum1, which appears to be a structural and functional homolog of Sic1. Based on the mutational data and sequence comparisons, we argue that Sic1 and p25rum1 are structurally distinct from the known mammalian CDK inhibitors, but may bind CDK complexes in a manner more closely resembling CDK substrates like the retinoblastoma and E2F proteins.

Key words Cyclin-dependent kinaseCyclin-dependent kinase inhibitorCell division cycleYeast

Copyright information

© Springer-Verlag Berlin Heidelberg 1999