FOXO1 represses Sprouty2 and Sprouty4 expression in endothelial cells to promote arterial specification and vascular remodeling in the mouse yolk sac

The establishment of a functional circulatory system is required for post-implantation development during murine embryogenesis. Previous studies in loss of function mouse models have shown that FOXO1, a Forkhead family transcription factor, is required for yolk sac vascular remodeling and survival beyond embryonic day (E) 11. Here, we demonstrate that loss of FoxO1 in E8.25 endothelial cells results in increased Sprouty2 and Sprouty4 transcripts, reduced expression of arterial genes, and decreased Flk1/Vegfr2 mRNA levels without affecting overall endothelial cell identity, survival, or proliferation. Using a Dll4-BAC-nlacZ reporter line, we found that one of the earliest expressed arterial genes, Delta like 4 ( Dll4) , is significantly reduced in the yolk sac of FoxO1 mutants without being substantially affected in the embryo proper. We show that in the yolk sac, FOXO1 not only binds directly to a subset of previously identified Sprouty2 gene regulatory elements (GREs), as well as newly identified, evolutionarily conserved Sprouty4 GREs, but can also repress their expression. Additionally, over expression of Sprouty4 in transient transgenic embryos largely recapitulates reduced expression of arterial genes seen in endothelial FoxO1 mutant mouse embryos. Together, these data reveal a novel role for FOXO1 as a key early transcriptional repressor controlling both pre-flow arterial specification and subsequent vessel remodeling within the murine yolk sac. ### Competing Interest Statement The authors have declared no competing interest.