bioRxivImmunologyPreprint
E-proteins set the threshold for optimal TCF1 expression during αβ T cell development.
A. Verma, B. Aylward, F. Ma, C. A. Sherman, L. Chopp, S. Shinton, R. Roy, S. Fahl, A. Contreras, B. Koenitzer, P. Awasthi, K. Mazan-Mamczarz, S. De, N. Ollikainen, X. Qiu, R. Bosselut, R. Sen, D. Wiest, J. M. Sen
Abstract
Expression of T Cell Factor-1 (TCF1), encoded by Tcf7, regulates lineage fate decisions during T cell development. Here we demonstrate that E-proteins control the threshold of TCF1 expression required for development of T cells. E-proteins bind to five elements (EPEs) in the Tcf7 locus. The third element, EPE3, interacts directly with Tcf7 promoter in Hi-ChIP analyses, suggesting it is an active enhancer. CRISPR-ablation of EPE3 reduces TCF1 protein expression in precursor thymocytes by 2-fold and dramatically impairs development of {beta} and {gamma}{delta} T cells. Single cell gene expression analysis identified differentiation blocks at multiple CD4-CD8- stages and subsequent transition to CD4+CD8+ stage. These data identify E-proteins and EPE3 as critical for the optimal TCF1 expression required for T cell development.
- organism: mouse
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: development & morphogenesis
- approach: experimental assay
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