Tyrosine kinases wee1 and mik1 as effectors of DNA replication checkpoint control

Prog Cell Cycle Res. 1996:2:91-7. doi: 10.1007/978-1-4615-5873-6_9.

Abstract

Cell cycle studies have revealed mechanisms that prevent cell division if DNA fails to be completely replicated or sustains damage. Here we focus on the evidence from yeast genetics that the wee1 and mik1 tyrosine kinases cooperate in the inhibitory phosphorylation of cdc2p, and the possibility that these kinases function in pathways that ensure the integrity of the genome prior to cell division. We also review the progress in cloning and analysing wee1-like tyrosine kinases from higher eukaryotes, and the evidence for and against their functioning in ensuring DNA replication prior to mitosis. Finally, we discuss the genes involved in these feedback controls and suggest that wee1p and mik1p might be the ultimate effectors that prevent mitosis when a checkpoint is triggered.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle Proteins*
  • DNA Damage
  • DNA Replication / physiology*
  • G2 Phase
  • Genes, Fungal
  • Humans
  • Nuclear Proteins*
  • Protein-Tyrosine Kinases / metabolism*
  • Schizosaccharomyces pombe Proteins*
  • Yeasts / genetics
  • Yeasts / metabolism

Substances

  • Cell Cycle Proteins
  • Nuclear Proteins
  • Schizosaccharomyces pombe Proteins
  • mik1 protein, S pombe
  • wee1 protein, S pombe
  • Protein-Tyrosine Kinases
  • WEE1 protein, human