Uncoupled cell cycle without mitosis induced by a protein kinase inhibitor, K-252a

J Cell Biol. 1991 Dec;115(5):1275-82. doi: 10.1083/jcb.115.5.1275.

Abstract

The staurosporine analogues, K-252a and RK-286C, were found to cause DNA re-replication in rat diploid fibroblasts (3Y1) without an intervening mitosis, producing tetraploid cells. Analysis of cells synchronized in early S phase in the presence of K-252a revealed that initiation of the second S phase required a lag period of 8 h after completion of the previous S phase. Reinitiation of DNA synthesis was inhibited by cycloheximide, actinomycin D, and serum deprivation, but not by Colcemid, suggesting that a functional G1 phase dependent on de novo synthesis of protein and RNA is essential for entry into the next S phase. In a src-transformed 3Y1 cell line, as well as other cell lines, giant cells containing polyploid nuclei with DNA contents of 16C to 32C were produced by continuous treatment with K-252a, indicating that the agent induced several rounds of the incomplete cell cycle without mitosis. Although the effective concentration of K-252a did not cause significant inhibition of affinity-purified p34cdc2 protein kinase activity in vitro, in vivo the full activation of p34cdc2 kinase during the G2/M was blocked by K-252a. On the other hand, the cyclic fluctuation of partially activated p34cdc2 kinase activity peaking in S phase still continued. These results suggest that a putative protein kinase(s) sensitive to K-252a plays an important role in the mechanism for preventing over-replication after completion of previous DNA synthesis. They also suggest that a periodic activation of p34cdc2 is required for S phases in the cell cycle without mitosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbazoles / pharmacology*
  • Cell Cycle / drug effects*
  • Cell Line
  • Diploidy
  • Fibroblasts / cytology
  • Flow Cytometry
  • Giant Cells / cytology
  • Indole Alkaloids
  • Mitosis
  • Protein Kinase Inhibitors*
  • Rats
  • S Phase / drug effects

Substances

  • Carbazoles
  • Indole Alkaloids
  • Protein Kinase Inhibitors
  • staurosporine aglycone