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Vol. 10, Issue 11, 3705-3715, November 1999


and
§
In Schizosaccharomyces pombe the MBF (DSC1)
complex mediates transcriptional activation at Start and is composed of
a common subunit called Cdc10 in combination with two alternative
DNA-binding partners, Res1 and Res2. It has been suggested that a
high-activity MBF complex (at G1/S) is switched to a low-activity
complex (in G2) by the incorporation of the negative regulatory subunit
Res2. We have analyzed MBF protein-protein interactions and find that both Res proteins are associated with Cdc10 throughout the cell cycle,
arguing against this model. Furthermore we demonstrate that Res2 is
capable of interacting with a mutant form of Cdc10 that has high
transcriptional activity. It has been shown previously that both Res
proteins are required for periodic cell cycle-regulated transcription.
Therefore a series of Res1-Res2 hybrid molecules was used to determine
the domains that are specifically required to regulate periodic
transcription. In Res2 the nature of the C-terminal region is critical,
and in both Res1 and Res2, a domain overlapping the N-terminal ankyrin
repeat and a recently identified activation domain is important for
mediating cell cycle-regulated transcription.
Laboratory of Gene Regulation, Imperial Cancer
Research Fund, London WC2A 3PX, United Kingdom; and *School of
Biochemistry and Genetics, The Medical School, The University of
Newcastle, Newcastle-upon-Tyne NE2 4HH, United Kingdom
Present address: The Paterson Institute
for Cancer Research, Christie Hospital NHS Trust, Wilmslow Road,
Manchester M20 4BX, UK.
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