Author:
Verma Anjali,Aylward Bridget,Ma Fei,Sherman Cheryl A.,Chopp Laura,Shinton Susan,Roy Roshni,Fahl Shawn,Contreras Alejandra,Koenitzer Byron,Awasthi Parirokh,Mazan-Mamczarz Krystyna,De Supriyo,Ollikainen Noah,Qiu Xiang,Bosselut Remy,Sen Ranjan,Wiest David L.,Sen Jyoti Misra
Abstract
AbstractExpression of T Cell Factor-1 (TCF1), encoded byTcf7,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 theTcf7locus. The third element, EPE3, interacts directly withTcf7promoter 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 αβ and γδ 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.
Publisher
Cold Spring Harbor Laboratory