Transcription factor dimerization activates the p300 acetyltransferase. (25th October 2018)

• Record Type: Journal Article
• Authors: Ortega, Esther; Rengachari, Srinivasan; Ibrahim, Ziad; Hoghoughi, Naghmeh; Gaucher, Jonathan; Holehouse, Alex; Khochbin, Saadi; Panne, Daniel
• Is Part Of: Nature. Volume 562:Number 7728(2018)
• Page Start: 538
• Page End: 544
• Publication Date: 2018-10-25
• Subjects: Science -- Periodicals; 505
• DOI: 10.1038/s41586-018-0621-1
• Languages: English
• ISSNs: 0028-0836

Abstract

Abstract The transcriptional co-activator p300 is a histone acetyltransferase (HAT) that is typically recruited to transcriptional enhancers and regulates gene expression by acetylating chromatin. Here we show that the activation of p300 directly depends on the activation and oligomerization status of transcription factor ligands. Using two model transcription factors, IRF3 and STAT1, we demonstrate that transcription factor dimerization enables thetrans -autoacetylation of p300 in a highly conserved and intrinsically disordered autoinhibitory lysine-rich loop, resulting in p300 activation. We describe a crystal structure of p300 in which the autoinhibitory loop invades the active site of a neighbouring HAT domain, revealing a snapshot of atrans -autoacetylation reaction intermediate. Substrate access to the active site involves the rearrangement of an autoinhibitory RING domain. Our data explain how cellular signalling and the activation and dimerization of transcription factors control the activation of p300, and therefore explain why gene transcription is associated with chromatin acetylation. The activation of the histone acetyltransferase p300 depends on the activation and oligomerization status of transcription factor ligands.