T-bet and GATA3 orchestrate Th1 and Th2 differentiation through lineage-specific targeting of distal regulatory elements

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作者
Aditi Kanhere
Arnulf Hertweck
Urvashi Bhatia
M. Refik Gökmen
Esperanza Perucha
Ian Jackson
Graham M. Lord
Richard G. Jenner
机构
[1] University College London,Division of Infection and Immunity and UCL Cancer Institute
[2] Guy’s and St Thomas’ Hospital and King’s College London,Department of Experimental Immunobiology and NIHR Biomedical Research Centre
[3] Present address: School of Biosciences,undefined
[4] University of Birmingham,undefined
[5] Edgbaston,undefined
[6] Birmingham B15 2TT,undefined
[7] UK,undefined
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T-bet and GATA3 regulate the CD4+ T cell Th1/Th2 cell fate decision but little is known about the interplay between these factors outside of the murine Ifng and Il4/Il5/Il13 loci. Here we show that T-bet and GATA3 bind to multiple distal sites at immune regulatory genes in human effector T cells. These sites display markers of functional elements, act as enhancers in reporter assays and are associated with a requirement for T-bet and GATA3. Furthermore, we demonstrate that both factors bind distal sites at Tbx21 and that T-bet directly activates its own expression. We also show that in Th1 cells, GATA3 is distributed away from Th2 genes, instead occupying T-bet binding sites at Th1 genes, and that T-bet is sufficient to induce GATA3 binding at these sites. We propose these aspects of T-bet and GATA3 function are important for Th1/Th2 differentiation and for understanding transcription factor interactions in other T cell lineage decisions.
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