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Peptidyl arginine deiminase 4 (PAD4) is a nuclear enzyme that converts arginine residues to citrulline. Although increasingly implicated in inflammatory disease and cancer, the mechanism of action of PAD4 and its functionally relevant pathways remains unclear. E2F transcription factors are a family of master regulators that coordinate gene expression during cellular proliferation and diverse cell fates. We show that E2F-1 is citrullinated by PAD4 in inflammatory cells. Citrullination of E2F-1 assists its chromatin association, specifically to cytokine genes in granulocyte cells. Mechanistically, citrullination augments binding of the BET (bromodomain and extra-terminal domain) family bromodomain reader BRD4 (bromodomain-containing protein 4) to an acetylated domain in E2F-1, and PAD4 and BRD4 coexist with E2F-1 on cytokine gene promoters. Accordingly, the combined inhibition of PAD4 and BRD4 disrupts the chromatin-bound complex and suppresses cytokine gene expression. In the murine collagen-induced arthritis model, chromatin-bound E2F-1 in inflammatory cells and consequent cytokine expression are diminished upon small-molecule inhibition of PAD4 and BRD4, and the combined treatment is clinically efficacious in preventing disease progression. Our results shed light on a new transcription-based mechanism that mediates the inflammatory effect of PAD4 and establish the interplay between citrullination and acetylation in the control of E2F-1 as a regulatory interface for driving inflammatory gene expression.

Original publication

DOI

10.1126/sciadv.1501257

Type

Journal article

Journal

Sci Adv

Publication Date

02/2016

Volume

2

Keywords

BRD4, E2F-1, PAD4, cancer, citrullination, immune response, inflammation, Acetylation, Animals, Arthritis, Experimental, Cell Line, Citrulline, Cytokines, E2F1 Transcription Factor, Gene Expression Regulation, HL-60 Cells, Humans, Hydrolases, Inflammation, Male, Mice, Mice, Inbred DBA, Nuclear Proteins, Promoter Regions, Genetic, Protein-Arginine Deiminases, RNA, Small Interfering, Recombinant Proteins, Transcription Factors