Affiliation:
1. Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas 77843-2128
Abstract
ABSTRACT
Approximately 800 transcripts in
Saccharomyces cerevisiae
are cell cycle regulated. The oscillation of ∼40% of these genes, including a prominent subclass involved in nutrient acquisition, is not understood. To address this problem, we focus on the mitosis-specific activation of the phosphate-responsive promoter,
PHO5
. We show that the unexpected mitotic induction of the
PHO5
acid phosphatase in rich medium requires the transcriptional activators Pho4 and Pho2, the cyclin-dependent kinase inhibitor Pho81, and the chromatin-associated enzymes Gcn5 and Snf2/Swi2.
PHO5
mitotic activation is repressed by addition of orthophosphate, which significantly increases cellular polyphosphate. Polyphosphate levels also fluctuate inversely with
PHO5
mRNA during the cell cycle, further substantiating an antagonistic link between this phosphate polymer and
PHO5
mitotic regulation. Moreover, deletion of
PHM3
, required for polyphosphate accumulation, leads to premature onset of
PHO5
expression, as well as an increased rate, magnitude, and duration of
PHO5
activation. Orthophosphate addition, however, represses mitotic
PHO5
expression in a
phm3
Δ strain. Thus, polyphosphate per se is not necessary to repress
PHO
transcription but, when present, replenishes cellular phosphate during nutrient depletion. These results demonstrate a dynamic mechanism of mitotic transcriptional regulation that operates mostly independently of factors that drive progression through the cell cycle.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
69 articles.
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