Affiliation:
1. Institute of Cell and Molecular Biosciences, Faculty of Medical Sciences, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH
2. Division of Yeast Genetics, National Institute for Medical Research, London NW7 1AA, United Kingdom
Abstract
ABSTRACT
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
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 G
1
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.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
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