Genetic and molecular characterization of Skb15, a highly conserved inhibitor of the fission yeast PAK, Shk1

Mol Cell. 2001 May;7(5):1095-101. doi: 10.1016/s1097-2765(01)00248-9.

Abstract

The p21-activated kinase, Shk1, is essential for viability, establishment and maintenance of cell polarity, and proper mating response in the fission yeast, Schizosaccharomyces pombe. Here we describe the characterization of a highly conserved, WD repeat protein, Skb15, which negatively regulates Shk1 in fission yeast. A null mutation in the skb15 gene is lethal and results in deregulation of actin polymerization and localization, microtubule biogenesis, and the cytokinetic machinery, as well as a substantial uncoupling of these processes from the cell cycle. Loss of Skb15 function is suppressed by partial loss of Shk1, demonstrating that negative regulation of Shk1 by Skb15 is required for proper execution of cytoskeletal remodeling and cytokinetic functions. A mouse homolog of Skb15 can substitute for its counterpart in fission yeast, demonstrating that Skb15 protein function has been substantially conserved through evolution.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / drug effects
  • Animals
  • Conserved Sequence
  • Cytoskeleton / drug effects
  • Evolution, Molecular
  • Fungal Proteins / genetics
  • Fungal Proteins / pharmacology*
  • Mice
  • Microtubules / drug effects
  • Mutation
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Schizosaccharomyces / chemistry*
  • Schizosaccharomyces pombe Proteins*
  • p21-Activated Kinases

Substances

  • Actins
  • Fungal Proteins
  • Schizosaccharomyces pombe Proteins
  • Skb15 protein, S pombe
  • Protein Serine-Threonine Kinases
  • p21-Activated Kinases
  • shk1 protein, S pombe