Fission yeast ste9, a homolog of Hct1/Cdh1 and fizzy-related, is a novel negative regulator of cell cycle progression during G1-phase

Kenji Kitamura, Hiromi Maekawa, Chikashi Shimoda

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91 Citations (Scopus)

Abstract

When proliferating fission yeast cells are exposed to nitrogen starvation, they initiate conjugation and differentiate into ascospores. Cell cycle arrest in the G1-phase is one of the prerequisites for cell differentiation, because conjugation occurs only in the pre-Start G1-phase. The role of ste9+ in the cell cycle progression was investigated. Ste9 is a WD-repeat protein that is highly homologous to Hct1/Cdh1 and Fizzy-related. The ste9 mutants were sterile because they were defective in cell cycle arrest in the G1-phase upon starvation. Sterility was partially suppressed by the mutation in cig2 that encoded the major G1/S cyclin. Although cells lacking Ste9 function grow normally, the ste9 mutation was synthetically lethal with the wee1 mutation. In the double mutants of ste9 cdc10(ts), cells arrested in G1-phase at the restrictive temperature, but the level of mitotic cyclin (Cdc13) did not decrease. In these cells, abortive mitosis occurred from the pre-Start G1-phase. Overexpression of Ste9 decreased the Cdc13 protein level and the H1-histone kinase activity. In these cells, mitosis was inhibited and an extra round of DNA replication occurred. Ste9 regulates G1 progression possibly by controlling the amount of the mitotic cyclin in the G1-phase.

Original languageEnglish
Pages (from-to)1065-1080
Number of pages16
JournalMolecular biology of the cell
Volume9
Issue number5
DOIs
Publication statusPublished - May 1998

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology

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