Fission yeast Ste9, a homolog of Hct1/Cdh1 and fizzy-related, is a novel negative regulator of cell cycle progression during G1-phase

被引:93
作者
Kitamura, K
Maekawa, H
Shimoda, C
机构
[1] Hiroshima Univ, Ctr Gene Sci, Higashihiroshima 7398527, Japan
[2] Osaka City Univ, Fac Sci, Dept Biol, Sumiyoshi Ku, Osaka 5588585, Japan
关键词
D O I
10.1091/mbc.9.5.1065
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
When proliferating fission yeast cells are exposed to nitrogen starvation, they initiate conjugation and differentiate into ascospores. Cell cycle arrest in the G(1)-phase is one of the prerequisites for cell differentiation, because conjugation occurs only in the pre-Start G(1)-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 G(1)-phase upon starvation. Sterility was partially suppressed by the mutation in cig2 that encoded the major G(1)/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 G(1)-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 G(1)-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 G(1) progression possibly by controlling the amount of the mitotic cyclin in the G(1)-phase.
引用
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页码:1065 / 1080
页数:16
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