bioRxiv preprint doi: https://doi.org/10.1101/417931; this version posted September 14, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Running Title: foxc1a and foxc1b in angiogenesis Title: foxc1a and foxc1b differentially regulate angiogenesis from arteries and veins by modulating Vascular Endothelial Growth Factor signalling Authors: Zhen Jiang1,2, Teri Evans4, Aaron M. Savage1,2, Matthew Loose4, Timothy J.A. Chico1,2, Fredericus J.M. van Eeden2,3, Robert N. Wilkinson1,2 1 Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, UK 2 The Bateson Centre, University of Sheffield, S10 2RX, UK 3 Department of Biomedical Science, University of Sheffield, S10 2TN, UK 4 School of Life Sciences, University of Nottingham, NG7 2UH, UK Corresponding author: Robert Wilkinson, Department of Infection, Immunity and Cardiovascular Disease, Medical School, University of Sheffield, S10 2RX, UK Email:
[email protected] Key words: foxc1, angiogenesis, VEGF, Notch, zebrafish, blood vessel Summary Statement foxc1a and foxc1b promote angiogenesis from veins and suppress angiogenesis from arteries by promoting competing pro-angiogenic Vascular Endothelial Growth Factor signalling, and anti-angiogenic Dll4/Notch signalling in zebrafish embryos. bioRxiv preprint doi: https://doi.org/10.1101/417931; this version posted September 14, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.