Affiliation:
1. Department of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48109-0606
Abstract
ABSTRACT
The baker’s yeast
Saccharomyces cerevisiae
possesses a single gene encoding heat shock transcription factor (HSF), which is required for the activation of genes that participate in stress protection as well as normal growth and viability. Yeast HSF (yHSF) contains two distinct transcriptional activation regions located at the amino and carboxyl termini. Activation of the yeast metallothionein gene,
CUP1
, depends on a nonconsensus heat shock element (HSE), occurs at higher temperatures than other heat shock-responsive genes, and is highly dependent on the carboxyl-terminal transactivation domain (CTA) of yHSF. The results described here show that the noncanonical (or gapped) spacing of GAA units in the
CUP1
HSE (HSE1) functions to limit the magnitude of
CUP1
transcriptional activation in response to heat and oxidative stress. The spacing in HSE1 modulates the dependence for transcriptional activation by both stresses on the yHSF CTA. Furthermore, a previously uncharacterized HSE in the
CUP1
promoter, HSE2, modulates the magnitude of the transcriptional activation of
CUP1
, via HSE1, in response to stress. In vitro DNase I footprinting experiments suggest that the occupation of HSE2 by yHSF strongly influences the manner in which yHSF occupies HSE1. Limited proteolysis assays show that HSF adopts a distinct protease-sensitive conformation when bound to the
CUP1
HSE1, providing evidence that the HSE influences DNA-bound HSF conformation. Together, these results suggest that
CUP1
regulation is distinct from that of other classic heat shock genes through the interaction of yHSF with two nonconsensus HSEs. Consistent with this view, we have identified other gene targets of yHSF containing HSEs with sequence and spacing features similar to those of
CUP1
HSE1 and show a correlation between the spacing of the GAA units and the relative dependence on the yHSF CTA.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
101 articles.
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