T-bet recruits P-TEFb to super-enhancers to regulate T helper cell differentiation (Agilent 1)

ABSTRACT: The transcription factor T-bet induces differentiation of CD4+ T cells into the Th1 lineage and also allows for a degree of functional plasticity. Here, we show that T-bet acts through super-enhancers to recruit the elongation factor P-TEFb. Th1-specific genes are poised for activation in Th2 cells and P-TEFb recruitment activates transcriptional elongation. T-bet also induces extensive P-TEFb binding at super-enhancers, where it acts to stimulate enhancer RNA transcription. P-TEFb inhibition selectively blocks activation of lineage-specific genes and reverses Th1-associated retinitis pathology. T-bet-mediated recruitment of P-TEFb to super-enhancers at otherwise poised genes provides a model for how lineage-specifying factors promote differentiation towards specific cell fates whilst maintaining a degree of functional plasticity. Transcriptional profiling of human Th1 and Th2 cells

ORGANISM(S): Homo sapiens

PROVIDER: GSE62484 | GEO | 2016/06/08

SECONDARY ACCESSION(S): PRJNA264231

REPOSITORIES: GEO