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Forkhead box A1 (FOXA1) is an FKHD family protein that plays pioneering roles in lineage-specific enhancer activation and gene transcription. Through genome-wide location analyses, here we show that FOXA1 expression and occupancy are, in turn, required for the maintenance of these epigenetic signatures, namely DNA hypomethylation and histone 3 lysine 4 methylation. Mechanistically, this involves TET1, a 5-methylcytosine dioxygenase. We found that FOXA1 induces TET1 expression via direct binding to its cis-regulatory elements. Further, FOXA1 physically interacts with the TET1 protein through its CXXC domain. TET1 thus co-occupies FOXA1-dependent enhancers and mediates local DNA demethylation and concomitant histone 3 lysine 4 methylation, further potentiating FOXA1 recruitment. Consequently, FOXA1 binding events are markedly reduced following TET1 depletion. Together, our results suggest that FOXA1 is not only able to recognize but also remodel the epigenetic signatures at lineage-specific enhancers, which is mediated, at least in part, by a feed-forward regulatory loop between FOXA1 and TET1.

Original publication

DOI

10.1093/nar/gkw498

Type

Journal article

Journal

Nucleic Acids Res

Publication Date

30/09/2016

Volume

44

Pages

8153 - 8164

Keywords

Cell Line, Tumor, Cell Lineage, Enhancer Elements, Genetic, Epigenesis, Genetic, HEK293 Cells, Hepatocyte Nuclear Factor 3-alpha, Humans, Mixed Function Oxygenases, Models, Biological, Protein Binding, Proto-Oncogene Proteins, Transcription, Genetic