The histone chaperone anti-silencing function 1 is a global regulator of transcription independent of passage through S phase.

TitleThe histone chaperone anti-silencing function 1 is a global regulator of transcription independent of passage through S phase.
Publication TypeJournal Article
Year of Publication2005
AuthorsZabaronick SR, Tyler JK
JournalMol Cell Biol
Volume25
Issue2
Pagination652-60
Date Published2005 Jan
ISSN0270-7306
KeywordsCell Cycle Proteins, Gene Expression Profiling, Gene Expression Regulation, Fungal, Histones, Molecular Chaperones, Oligonucleotide Array Sequence Analysis, Ribonucleases, S Phase, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Transcription, Genetic
Abstract

We investigated the function of the histone H3/H4 chaperones anti-silencing function 1 (Asf1p) and chromatin assembly factor 1 (CAF-1) in global transcriptional regulation in budding yeast. Deletion of ASF1 or CAF-1 components led to global transcriptional misregulation, both activation and repression, of genes scattered throughout the 16 yeast chromosomes. To investigate direct effects on gene regulation, we developed an approach to destabilize Asf1p that results in its rapid degradation within minutes of transcriptional repression. Upon degradation of Asf1p, rapid global changes in gene expression occur without the requirement for passage through S phase or de novo protein synthesis. In particular, we demonstrate that the previously reported influence of Asf1p on histone gene expression is not a direct effect of loss of Asf1p. These data indicate that the histone chaperones CAF-1 and Asf1p regulate the gene expression of a broad array of genes in yeast and, in the case of Asf1p, this is likely to be due to a direct role in chromatin modulation during transcriptional regulation.

DOI10.1128/MCB.25.2.652-660.2005
Alternate JournalMol Cell Biol
PubMed ID15632066
PubMed Central IDPMC543432
Grant ListR01 GM064475 / GM / NIGMS NIH HHS / United States
GM64475 / GM / NIGMS NIH HHS / United States
Related Faculty: 
Jessica K. Tyler, Ph.D.

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