The Schizosaccharomyces pombe cdc5(+) gene was identified in the first
screen for cell division cycle mutants in this yeast. The cdc5(+) gen
e was reported to be required for nuclear division but because of its
modest elongation and leaky nature at the non-permissive temperature,
it was not investigated further. Here, we report the characterization
of the single allele of this gene, cdc5-120, in more detail. The mutan
t arrests with a 2N DNA content and a single interphase nucleus. Furth
er genetic analyses suggest that cdc5(+) gene function is essential in
the G(2) phase of the cell cycle. We have cloned and sequenced the cd
c5(+) gene. The deduced protein sequence predicts that Cdc5 is an 87 k
Da protein and contains a region sharing significant homology with the
DNA binding domain of the Myb family of transcription factors. Deleti
on mapping of the cdc5(+) gene has shown that the N-terminal 232 amino
acids of the protein, which contain the Myb-related region, are suffi
cient to complement the cdc5(ts) strain. A cdc5 null mutant was genera
ted by homologous recombination. Haploid cells lacking cdc5(+) are inv
iable, indicating that cdc5(+) is an essential gene. A fusion protein
consisting of bacterial glutathione S-transferase joined in-frame to t
he N-terminal 127 amino acids of the Cdc5 protein is able to bind to D
NA cellulose at low salt concentrations. This evidence suggests that c
dc5(+) might encode a transcription factor whose activity is required
for cell cycle progression and growth during G(2).