| Literature DB >> 29466756 |
John L Johnson1, Georgios Georgakilas1, Jelena Petrovic2, Makoto Kurachi3, Stanley Cai1, Christelle Harly4, Warren S Pear2, Avinash Bhandoola4, E John Wherry3, Golnaz Vahedi5.
Abstract
T cell development is orchestrated by transcription factors that regulate the expression of genes initially buried within inaccessible chromatin, but the transcription factors that establish the regulatory landscape of the T cell lineage remain unknown. Profiling chromatin accessibility at eight stages of T cell development revealed the selective enrichment of TCF-1 at genomic regions that became accessible at the earliest stages of development. TCF-1 was further required for the accessibility of these regulatory elements and at the single-cell level, it dictated a coordinate opening of chromatin in T cells. TCF-1 expression in fibroblasts generated de novo chromatin accessibility even at chromatin regions with repressive marks, inducing the expression of T cell-restricted genes. These results indicate that a mechanism by which TCF-1 controls T cell fate is through its widespread ability to target silent chromatin and establish the epigenetic identity of T cells.Entities:
Keywords: Lineage-determining transcription factor; T cell development; TCF-1; chromatin accessibility; epigenetics; nucleosomes; repressed chromatin; reprogramming; single-cell epigenomics
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Year: 2018 PMID: 29466756 PMCID: PMC5824646 DOI: 10.1016/j.immuni.2018.01.012
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745