Journal
EUKARYOTIC CELL
Volume 3, Issue 4, Pages 944-954Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/EC.3.4.944-954.2004
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Funding
- Medical Research Council [MC_U117531948] Funding Source: researchfish
- Medical Research Council [MC_U117531948] Funding Source: Medline
- MRC [MC_U117531948] Funding Source: UKRI
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In eukaryotes the regulation of gene expression plays a key role in controlling cell cycle progression. Here, we demonstrate that a forkhead transcription factor, Fkh2, regulates the periodic expression of cdc15(+) and spo12(+) in the M and G(1) phases of the cell division cycle in the fission yeast Schizosaccharomycespombe. We also show that Fkh2 is important for several cell cycle processes, including cell morphology and cell separation, nuclear structure and migration, and mitotic spindle function. We find that the expression of fkh2(+) is itself regulated in a cell cycle-dependent manner in G, coincident with the expression of cdc18(+), a Cdc10-regulated gene. However,fkh2(+) expression is independent of Cdc10 function. Fkh2 was found to be phosphorylated during the cell division cycle, with a timing that suggests that this posttranslational modification is important for cdc15(+) and spo12(+) expression. Related forkhead proteins regulate G(2) and M phase-specific gene expression in the evolutionarily distant Saccharomyces cerevisiae, suggesting that these proteins play conserved roles in regulating cell cycle processes in eukaryotes.
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