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Vol. 11, Issue 9, 3205-3217, September 2000

and
*Department of Biophysics and Biochemistry, Graduate School of
Science, and Schizosaccharomyces pombe ste11 encodes a
high-mobility group family transcriptional activator that is pivotal in
sexual development. Transcription of ste11 is induced by
starvation of nutrients via a decrease of the cAMP-dependent protein
kinase (PKA) activity. Here we report the identification of a novel
transcription factor, Rst2p, that directly regulates
ste11 expression. Cells in which the rst2
gene was disrupted expressed ste11 poorly and were
sterile, and this sterility could be suppressed by artificial
expression of ste11. Disruption of rst2
suppressed hypermating and hypersporulation in the PKA-null mutant,
whereas overexpression of rst2 induced sexual
development in the PKA-activated mutant. Cloning analysis indicated
that Rst2p was a Cys2His2 zinc-finger protein
carrying 567 amino acid residues. Rst2p could bind specifically to a
stress response element-like cis element located in the
ste11 promoter region, which was important for
ste11 expression. Meanwhile, transcription of
ste11 was reduced significantly by a defective mutation
in itself. An artificial supply of functional Ste11p circumvented this
reduction. A complete Ste11p-binding motif (TR box) found in the
promoter region was necessary for the full expression of ste11, suggesting that Ste11p is involved in the
activation of ste11. We conclude that transcription of
ste11 is under autoregulation in addition to control
through the PKA-Rst2p pathway.
Molecular Genetics Research Laboratory,
University of Tokyo, Hongo, Tokyo 113-0033, Japan
Corresponding author. E-mail address:
myamamot{at}ims.u-tokyo.ac.jp.
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