Affiliation:
1. Department of Biomedical Sciences, State University of New York at Albany School of Public Health
2. Laboratory of Developmental Genetics, Wadsworth Center, New York State Department of Health, Albany, New York 12201-2002
Abstract
ABSTRACT
The histone H3 amino terminus, but not that of H4, is required to prevent the constitutively bound activator Cha4 from remodeling chromatin and activating transcription at the
CHA1
gene in
Saccharomyces cerevisiae
. Here we show that neither the modifiable lysine residues nor any specific region of the H3 tail is required for repression of
CHA1
. We then screened for histone H3 mutations that cause derepression of the uninduced
CHA1
promoter and identified six mutants, three of which are also temperature-sensitive mutants and four of which exhibit a
sin
−
phenotype. Histone mutant levels were similar to that of wild-type H3, and the mutations did not cause gross alterations in nucleosome structure. One specific and strongly derepressing mutation, H3 A111G, was examined in depth and found to cause a constitutively active chromatin configuration at the uninduced
CHA1
promoter as well as at the
ADH2
promoter. Transcriptional derepression and altered chromatin structure of the
CHA1
promoter depend on the activator Cha4. These results indicate that modest perturbations in distinct regions of the nucleosome can substantially affect the repressive function of chromatin, allowing activation in the absence of a normal inducing signal (at
CHA1
) or of Swi/Snf (resulting in a
sin
−
phenotype).
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
11 articles.
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