The NFIA-ETO2 fusion blocks erythroid maturation and induces pure erythroid leukemia in cooperation with mutant TP53

The NFIA-ETO2 fusion is the product of a t(1;16)(p31;q24) chromosomal translocation, so far, exclusively found in pediatric patients with pure erythroid leukemia (PEL). To address the role for the pathogenesis of the disease, we facilitated the expression of the NFIA-ETO2 fusion in murine erythroblasts (EBs). We observed that NFIA-ETO2 significantly increased proliferation and impaired erythroid differentiation of murine erythroleukemia cells and of primary fetal liver-derived EBs. However, NFIA-ETO2-expressing EBs acquired neither aberrant in vitro clonogenic activity nor disease-inducing potential upon transplantation into irradiated syngenic mice. In contrast, in the presence of 1 of the most prevalent erythroleukemia-associated mutations, TP53(R248Q), expression of NFIA-ETO2 resulted in aberrant clonogenic activity and induced a fully penetrant transplantable PEL-like disease in mice. Molecular studies support that NFIA-ETO2 interferes with erythroid differentiation by preferentially binding and repressing erythroid genes that contain NFI binding sites and/or are decorated by ETO2, resulting in a activity shift from GATA-to ETS-motif-containing target genes. In contrast, TP53(R248Q) does not affect erythroid differentiation but provides self-renewal and survival potential, mostly via downregulation of known TP53 targets. Collectively, our work indicates that NFIA-ETO2 initiates PEL by suppressing gene expression programs of terminal erythroid differentiation and cooperates with TP53 mutation to induce erythroleukemia.

Automated summary

The NFIA-ETO2 fusion is a chromosomal translocation found exclusively in pediatric patients with pure erythroid leukemia (PEL). The fusion protein impairs erythroid differentiation and promotes proliferation in murine erythroblasts and fetal liver-derived erythroblasts. However, it does not induce disease upon transplantation into mice. In the presence of TP53(R248Q) mutation, NFIA-ETO2 acquires clonogenic activity and induces a transplantable PEL-like disease. Molecular studies reveal that NFIA-ETO2 represses erythroid differentiation by targeting genes with NFI binding sites and ETO2 modifications, while TP53(R248Q) enhances self-renewal and survival potential.