Kinase-independent activity of Cdc2/cyclin A prevents the S phase in the Drosophila cell cycle

Genes Cells. 1999 Feb;4(2):111-22. doi: 10.1046/j.1365-2443.1999.00243.x.

Abstract

Background: The Cdc2-dependent inhibition of S phase is required in G2 for the correct ordering of the S and M phases in yeasts and Drosophila. This function of Cdc2 has been ascribed to its ability to phosphorylate replication factors to prevent the assembly of a preinitiation complex at the origin of replication. Whether this is the sole mechanism of S phase inhibition by Cdc2 in higher metazoans is not known because the pleiotropic functions of this essential cell cycle regulator make genetic analysis difficult.

Results: We show that Cdc2 co-expressed with Cyclin A inhibits the S phase in Drosophila salivary glands and diploid abdominal histoblasts. A kinase defective mutant of Cdc2 failed to promote mitosis, but was still able to inhibit the S phase with the same efficiency as the wild-type protein. In addition, Cdc2 and Cyclin A cooperatively inhibit transcriptional activation by the essential S phase regulator E2F. Cdc2 binds to E2F in vitro, and post-transcriptionally promotes its accumulation in vivo. Furthermore, the inhibitory effect of Cdc2 on S phase is overridden by E2F.

Conclusion: The inhibition of S phase by Cdc2 is achieved in part by a kinase-independent mechanism, which is likely to be mediated by the inhibition of E2F.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen
  • Animals
  • CDC2 Protein Kinase / genetics
  • CDC2 Protein Kinase / metabolism*
  • Carrier Proteins*
  • Cell Cycle / physiology*
  • Cell Cycle Proteins*
  • Cyclin A / metabolism*
  • DNA Replication
  • DNA-Binding Proteins*
  • Diploidy
  • Drosophila / genetics
  • Drosophila / metabolism*
  • Drosophila Proteins*
  • E2F Transcription Factors
  • G2 Phase / physiology
  • Proliferating Cell Nuclear Antigen / genetics
  • Proliferating Cell Nuclear Antigen / metabolism
  • Retinoblastoma-Binding Protein 1
  • S Phase / physiology*
  • Salivary Glands / cytology
  • Salivary Glands / metabolism
  • Trans-Activators*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • Cyclin A
  • DNA-Binding Proteins
  • Dp transcription factor, Drosophila
  • Drosophila Proteins
  • E2F Transcription Factors
  • Proliferating Cell Nuclear Antigen
  • Retinoblastoma-Binding Protein 1
  • Trans-Activators
  • Transcription Factors
  • CDC2 Protein Kinase