Nature CommunicationsMolecular BiologyPeer-reviewed journal article
Positioning of nucleosomes containing γ-H2AXprecedes active DNA demethylation and transcription initiation
Stephanie DoberschiD, Karla RubioiD, Indrabahadur SinghiD, Stefan GüntheriD, Johannes GraumanniD, Julio CorderoiD, Rafael Castillo‐Negrete, Minh Bao HuynhiD, Aditi MehtaiD, Peter BraubachiD, Héctor A. Cabrera-FuentesiD, Jürgen BernhageniD, Cho‐Ming ChaoiD, Savério BellusciiD, Andreas GüntheriD, Klaus Preissner, Sita KugeliD, Gergana D. DobrevaiD, Małgorzata WygreckaiD, Thomas W BrauniD, Dulce Papy-GarcíaiD, Guillermo BarretoiD
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Abstract
In addition to nucleosomes, chromatin contains non-histone chromatin-associated proteins, of which the high-mobility group (HMG) proteins are the most abundant. Chromatin-mediated regulation of transcription involves DNA methylation and histone modifications. However, the order of events and the precise function of HMG proteins during transcription initiation remain unclear. Here we show that HMG AT-hook 2 protein (HMGA2) induces DNA nicks at the transcription start site, which are required by the histone chaperone FACT (facilitates chromatin transcription) complex to incorporate nucleosomes containing the histone variant H2A.X. Further, phosphorylation of H2A.X at S139 ({gamma}-H2AX) is required for repair-mediated DNA demethylation and transcription activation. The relevance of these findings is demonstrated within the context of TGFB1 signaling and idiopathic pulmonary fibrosis, suggesting therapies against this lethal disease. Our data support that chromatin opening during transcriptional initiation involves intermediates with DNA breaks that subsequently require DNA repair mechanisms to ensure the integrity of the genome.
- organism: human
- assay: DNA methylation
- assay: ChIP-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: experimental assay
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