Stage-specific epigenetic regulation of CD4 expression by coordinated enhancer elements during T cell development

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作者
Priya D. Issuree
Kenneth Day
Christy Au
Ramya Raviram
Paul Zappile
Jane A. Skok
Hai-Hui Xue
Richard M. Myers
Dan R. Littman
机构
[1] New York University School of Medicine,The Kimmel Center for Biology and Medicine of the Skirball Institute
[2] Hudson Alpha Institute for Biotechnology,Howard Hughes Medical Institute
[3] New York University School of Medicine,Department of Pathology
[4] New York University School of Medicine,Genome Technology Center
[5] New York University School of Medicine,Department of Microbiology and Immunology, Carver College of Medicine
[6] University of Iowa,Intermountain Precision Genomics
[7] Translational Science Center,undefined
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The inheritance of gene expression patterns is dependent on epigenetic regulation, but the establishment and maintenance of epigenetic landscapes during T cell differentiation are incompletely understood. Here we show that two stage-specific Cd4 cis-elements, the previously characterized enhancer E4p and a novel enhancer E4m, coordinately promote Cd4 transcription in mature thymic MHC-II-specific T cells, in part through the canonical Wnt pathway. Specifically, E4p licenses E4m to orchestrate DNA demethylation by TET1 and TET3, which in turn poises the Cd4 locus for transcription in peripheral T cells. Cd4 locus demethylation is important for subsequent Cd4 transcription in activated peripheral T cells wherein these cis-elements become dispensable. By contrast, in developing thymocytes the loss of TET1/3 does not affect Cd4 transcription, highlighting an uncoupled event between transcription and epigenetic modifications. Together our findings reveal an important function for thymic cis-elements in governing gene expression in the periphery via a heritable epigenetic mechanism.
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