A dual cis-regulatory code links IRF8 to constitutive and inducible gene expression in macrophages.

ABSTRACT: IThe transcription factor (TF) interferon regulatory factor 8 (IRF8) controls both developmental and inflammatory stimulus-inducible genes in macrophages, but the mechanisms underlying these two different functions are largely unknown. One possibility is that these different roles are linked to the ability of IRF8 to bind alternative DNA sequences. We found that IRF8 is recruited to distinct sets of DNA consensus sequences before and after lipopolysaccharide (LPS) stimulation. In resting cells, IRF8 was mainly bound to composite sites together with the master regulator of myeloid development PU.1. Basal IRF8M-bM-^@M-^SPU.1 binding maintained the expression of a broad panel of genes essential for macrophage functions (such as microbial recognition and response to purines) and contributed to

ORGANISM(S): Mus musculus

SUBMITTER: Alberto Termanini 

PROVIDER: E-GEOD-56122 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress