Sign in
ImmunologybioRxiv
Preprint

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.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.