Chromatin disassembly from the PHO5 promoter is essential for the recruitment of the general transcription machinery and coactivators.

TitleChromatin disassembly from the PHO5 promoter is essential for the recruitment of the general transcription machinery and coactivators.
Publication TypeJournal Article
Year of Publication2007
AuthorsAdkins MW, Williams SK, Linger J, Tyler JK
JournalMol Cell Biol
Volume27
Issue18
Pagination6372-82
Date Published2007 Sep
ISSN0270-7306
KeywordsAcid Phosphatase, Chromatin, Models, Genetic, Promoter Regions, Genetic, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Trans-Activators, Transcription, Genetic
Abstract

The disassembly of promoter nucleosomes appears to be a general property of highly transcribed eukaryotic genes. We have previously shown that the disassembly of chromatin from the promoters of the Saccharomyces cerevisiae PHO5 and PHO8 genes, mediated by the histone chaperone anti-silencing function 1 (Asf1), is essential for transcriptional activation upon phosphate depletion. This mechanism of transcriptional regulation is shared with the ADY2 and ADH2 genes upon glucose removal. Promoter chromatin disassembly by Asf1 is required for recruitment of TBP and RNA polymerase II, but not the Pho4 and Pho2 activators. Furthermore, accumulation of SWI/SNF and SAGA at the PHO5 promoter requires promoter chromatin disassembly. By contrast, the requirement for SWI/SNF and SAGA to facilitate Pho4 activator recruitment to the nucleosome-buried binding site in the PHO5 promoter occurs prior to chromatin disassembly and is distinct from the stable recruitment of SWI/SNF and SAGA that occurs after chromatin disassembly.

DOI10.1128/MCB.00981-07
Alternate JournalMol Cell Biol
PubMed ID17620413
PubMed Central IDPMC2099613
Grant ListR01 GM064475 / GM / NIGMS NIH HHS / United States
GM64475 / GM / NIGMS NIH HHS / United States
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Jessica K. Tyler, Ph.D.

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