bioRxivEvolutionary Biology
Expansion and collapse of VEGF diversity in major clades of the animal kingdom
Abstract
The vascular endothelial growth factor (VEGF) family comprises in vertebrates five or six members: VEGF(-A), PlGF, VEGF-B, VEGF-C, VEGF-D, and - in venomous reptiles - VEGF-F. They fulfill mainly functions for the blood and lymphatic vascular systems. Together with the platelet-derived growth factors (PDGF-A to -D), they form the PDGF/VEGF subgroup among cystine-knot growth factors. Despite an absent vascular system in most invertebrates, PDGF/VEGF-like molecules have been found in, e.g., Drosophila melanogaster and Caenorhabditis elegans. The evolutionary relationship between PDGF and VEGF growth factors has only been addressed by older analyses, which were limited by the sparse sequencing data at the time. Here we perform a comprehensive analysis of the occurrence of PDGF/VEGF-like growth factors (PVFs) throughout all animal phyla and propose a likely phylogenetic tree. The three major vertebrate whole genome duplications play a role in the expansion of PDGF/VEGF diversity, but several limited duplications are necessary to account for the temporal pattern of emergence. The phylogenetically oldest PVFs likely featured a C-terminus with a BR3P signature, a hallmark of the modern-day lymphangiogenic growth factors VEGF-C and VEGF-D. Some of the younger VEGF genes appeared completely absent in some clades, e.g., functional VEGFB genes in the clade Archosauria, which includes crocodiles, birds, and other dinosaurs, and pgf in amphibians. The lack of precise counterparts for human genes poses limitations but also offers opportunities for research using organisms that diverge considerably from humans if the goal is to understand human physiology. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=181 HEIGHT=200 SRC="FIGDIR/small/507521v2_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@16b1abforg.highwire.dtl.DTLVardef@a91012org.highwire.dtl.DTLVardef@15e4994org.highwire.dtl.DTLVardef@1309753_HPS_FORMAT_FIGEXP M_FIG Sources for the graphical abstract: 326 MYA and older [1] 272-240 MYA [2] 235-65 MYA [3] C_FIG
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.
Related papers
- Cross-family interactions of vascular endothelial growth factors and platelet-derived growth factors on the endothelial cell surface: A computational model
Yunjeong Lee, Yingye Fang, … P. I. Imoukhuede·bioRxiv·Feb 27, 2025
- Phylogenetic evidence for independent origins of GDF1 and GDF3 genes in amphibians and mammals
J. C. Opazo, K. Zavala·bioRxiv·Jun 16, 2018
- Cross-family Signaling: PDGF Mediates VEGFR Activation and Endothelial Function
Xinming Liu, Yingye Fang, … P.I. Imoukhuede·bioRxiv·Feb 27, 2025
- Phased affinity-controlled delivery of vascular endothelial growth factor, fibroblast growth factor-2, and platelet derived growth factor enhances in vitro angiogenesis
Justin E. Svendsen, Chandler L. Asnes, … Marian H. Hettiaratchi·Journal of Controlled ReleasePeer-reviewed·Jul 14, 2026
- An evolutionarily conserved role for VEGF signaling in the expansion of non-vascular tissue during regeneration.
Aaron M. Savage, Alexandra C. Wagner, … Jessica L. Whited·bioRxiv·Oct 1, 2024
- The RAF oncogenes of vertebrates are ohnologs that derive from the two rounds of whole-genome duplications early in vertebrate evolution
A. Coward Black, M. C. Bailey, … F. Hoffmann·bioRxiv·Sep 12, 2019