Affiliation:
1. Department of Microbiology and Molecular Genetics, University of Texas Medical School, Houston, Texas 77030
2. Universität des Saarlandes, Medizinische Biochemie und Molekularbiologie, Gebäude 61.4, D-66421 Homburg/Saar, Germany
Abstract
ABSTRACT
Cells must rapidly sense and respond to a wide variety of potentially cytotoxic external stressors to survive in a constantly changing environment. In a search for novel genes required for stress tolerance in
Saccharomyces cerevisiae
, we identified the uncharacterized open reading frame YER139C as a gene required for growth at 37°C in the presence of the heat shock mimetic formamide. YER139C encodes the closest yeast homolog of the human RPAP2 protein, recently identified as a novel RNA polymerase II (RNAPII)-associated factor. Multiple lines of evidence support a role for this gene family in transcription, prompting us to rename YER139C
RTR1
(
r
egulator of
tr
anscription). The core RNAPII subunits
RPB5, RPB7
, and
RPB9
were isolated as potent high-copy-number suppressors of the
rtr1
Δ temperature-sensitive growth phenotype, and deletion of the nonessential subunits
RPB4
and
RPB9
hypersensitized cells to
RTR1
overexpression. Disruption of
RTR1
resulted in mycophenolic acid sensitivity and synthetic genetic interactions with a number of genes involved in multiple phases of transcription. Consistently,
rtr1
Δ cells are defective in inducible transcription from the
GAL1
promoter. Rtr1 constitutively shuttles between the cytoplasm and nucleus, where it physically associates with an active RNAPII transcriptional complex. Taken together, our data reveal a role for members of the RTR1/RPAP2 family as regulators of core RNAPII function.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
39 articles.
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