Coordinated demethylation of H3K9 and H3K27 is required for rapid inflammatory responses of endothelial cells.

ABSTRACT: Histone H3 lysine-9 di-methylation (H3K9me2) and lysine-27 tri-methylation (H3K27me3) are linked to repression of gene expression, but the functions of repressive histone methylation dynamics during inflammatory responses remain enigmatic. Here, we report that lysine demethylases 7A (KDM7A) and 6A (UTX) play crucial roles in tumor necrosis factor (TNF)-? signaling in endothelial cells (ECs), where they are regulated by a novel TNF-?-responsive microRNA, miR-3679-5p. TNF-? rapidly induces co-occupancy of KDM7A and UTX at nuclear factor kappa-B (NF-?B)-associated elements in human ECs. KDM7A and UTX demethylate H3K9me2 and H3K27me3, respectively, and are both required for activation of NF-?B-dependent inflammatory genes. Chromosome conformation capture-based methods furthermore uncover incre

SUBMITTER: Yoshiki Higashijima 

PROVIDER: S-SCDT-EMBOJ-2019-103949 | biostudies-other |

REPOSITORIES: biostudies-other