Molecular and Cellular Biology, August 1999, p. 5267-5278, Vol. 19, No. 8
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada M5S 1A8,1 and Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 117242
Received 19 March 1999/Returned for modification 28 April 1999/Accepted 30 April 1999
In Saccharomyces cerevisiae, gene expression in the
late G1 phase is activated by two transcription factors,
SBF and MBF. SBF contains the Swi4 and Swi6 proteins and activates the
transcription of G1 cyclin genes, cell wall biosynthesis
genes, and the HO gene. MBF is composed of Mbp1 and Swi6
and activates the transcription of genes required for DNA synthesis.
Mbp1 and Swi4 are the DNA binding subunits for MBF and SBF, while the
common subunit, Swi6, is presumed to play a regulatory role in both
complexes. We show that Stb1, a protein first identified in a
two-hybrid screen with the transcriptional repressor Sin3, binds Swi6
in vitro. The STB1 transcript was cell cycle periodic and
peaked in late G1 phase. In vivo accumulation of Stb1
phosphoforms was dependent on CLN1, CLN2, and
CLN3, which encode G1-specific cyclins for the
cyclin-dependent kinase Cdc28, and Stb1 was phosphorylated by Cln-Cdc28
kinases in vitro. Deletion of STB1 caused an exacerbated
delay in G1 progression and the onset of Start
transcription in a cln3
strain. Our results suggest a
role for STB1 in controlling the timing of Start
transcription that is revealed in the absence of the G1
regulator CLN3, and they implicate Stb1 as an in vivo
target of G1-specific cyclin-dependent kinases.
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