O-GlcNAcylation enhances FOXO4 transcriptional regulation in response to stress.

Abstract The FOXO4 transcription factor plays an important role in cell survival in response to oxidative stress. The regulation of FOXO4 is orchestrated by post-translational modifications including phosphorylation, acetylation, and ubiquitination. Here, we demonstrate that O -GlcNAcylation also contributes to the FOXO4-dependent oxidative stress response. We show that hydrogen peroxide treatment of HEK293 cells increases FOXO4 association with OGT, the enzyme that adds O -GlcNAc to proteins, causing FOXO4 O -GlcNAcylation and enhanced transcriptional activity under acute oxidative stress. O -GlcNAcylation is known to be protective for cells under stress conditions, including oxidative stress. Our data provide a mechanism of FOXO4 anti-oxidative protection through O -GlcNAcylation. Structured summary MINT- 7299700 , MINT- 7299716 : Foxo4 (uniprotkb: Q9WVH3 ) physically interacts (MI: 0915 ) with Ogt (uniprotkb: P56558 ) by anti tag coimmunoprecipitation (MI: 0007 ) MINT- 7299691 : Ogt (uniprotkb: O15294 ) physically interacts (MI: 0915 ) with Foxo4 (uniprotkb: P98177 ) by anti bait coimmunoprecipitation (MI: 0006 )