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Eukaryotic Cell, August 2004, p. 944-954, Vol. 3, No. 4
1535-9778/04/$08.00+0 DOI: 10.1128/EC.3.4.944-954.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Aline Pic-Taylor,1,
Simon K. Whitehall,1 Kate A. Martin,1 Jonathan B. A. Millar,2 Janet Quinn,1 and Brian A. Morgan1*
Institute of Cell and Molecular Biosciences, Faculty of Medical Sciences, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH,1 Division of Yeast Genetics, National Institute for Medical Research, London NW7 1AA, United Kingdom2
Received 27 January 2004/ Accepted 27 April 2004
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 G1 phases of the cell division cycle in the fission yeast Schizosaccharomyces pombe. 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 G1 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 G2 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.
R.B. and A.P.-T. contributed equally to this work.
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