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American Society for Cell Biology, Molecular Biology of the Cell, 23(20), p. 4976-4984

DOI: 10.1091/mbc.e09-04-0295

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Heat-Shock Factor 1 Controls Genome-wide Acetylation in Heat-shocked Cells

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

A major regulatory function has been evidenced here for HSF1, the key transcription factor of the heat-shock response, in a large-scale remodeling of the cell epigenome. Indeed, upon heat shock, HSF1, in addition to its well-known transactivating activities, mediates a genome-wide and massive histone deacetylation. Investigating the underlying mechanisms, we show that HSF1 specifically associates with and uses HDAC1 and HDAC2 to trigger this heat-shock–dependent histone deacetylation. This work therefore identifies HSF1 as a master regulator of global chromatin acetylation and reveals a cross-talk between HSF1 and histone deacetylases in the general control of genome organization in response to heat shock.