| Literature DB >> 26982363 |
Sören Boller1, Senthilkumar Ramamoorthy1, Duygu Akbas1, Robert Nechanitzky1, Lukas Burger2, Rabih Murr3, Dirk Schübeler3, Rudolf Grosschedl4.
Abstract
Lymphopoiesis requires the activation of lineage-specific genes embedded in naive, inaccessible chromatin or in primed, accessible chromatin. The mechanisms responsible for de novo gain of chromatin accessibility, known as "pioneer" function, remain poorly defined. Here, we showed that the EBF1 C-terminal domain (CTD) is required for the regulation of a specific gene set involved in B cell fate decision and differentiation, independently of activation and repression functions. Using genome-wide analysis of DNaseI hypersensitivity and DNA methylation in multipotent Ebf1(-/-) progenitors and derivative EBF1wt- or EBF1ΔC-expressing cells, we found that the CTD promoted chromatin accessibility and DNA demethylation in previously naive chromatin. The CTD allowed EBF1 to bind at inaccessible genomic regions that offer limited co-occupancy by other transcription factors, whereas the CTD was dispensable for EBF1 binding at regions that are occupied by multiple transcription factors. Thus, the CTD enables EBF1 to confer permissive lineage-specific changes in progenitor chromatin landscape.Entities:
Keywords: B lymphopoiesis; DNA methylation; DNaseI hypersensitivity; EBF1; chromatin; pioneer transcription factor
Mesh:
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Year: 2016 PMID: 26982363 DOI: 10.1016/j.immuni.2016.02.021
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745