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Expansion and collapse of VEGF diversity in major clades of the animal kingdom
Together with the platelet-derived growth factors (PDGFs), the vascular endothelial growth factors (VEGFs) form the PDGF/VEGF subgroup among cystine knot growth factors. The evolutionary relationships within this subgroup have not been examined thoroughly to date. Here, we comprehensively analyze th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328876/ https://www.ncbi.nlm.nih.gov/pubmed/37017884 http://dx.doi.org/10.1007/s10456-023-09874-9 |
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author | Rauniyar, Khushbu Bokharaie, Honey Jeltsch, Michael |
author_facet | Rauniyar, Khushbu Bokharaie, Honey Jeltsch, Michael |
author_sort | Rauniyar, Khushbu |
collection | PubMed |
description | Together with the platelet-derived growth factors (PDGFs), the vascular endothelial growth factors (VEGFs) form the PDGF/VEGF subgroup among cystine knot growth factors. The evolutionary relationships within this subgroup have not been examined thoroughly to date. Here, we comprehensively analyze the PDGF/VEGF growth factors throughout all animal phyla and propose a phylogenetic tree. Vertebrate whole-genome duplications play a role in expanding PDGF/VEGF diversity, but several limited duplications are necessary to account for the temporal pattern of emergence. The phylogenetically oldest PDGF/VEGF-like growth factor likely featured a C-terminus with a BR3P signature, a hallmark of the modern-day lymphangiogenic growth factors VEGF-C and VEGF-D. Some younger VEGF genes, such as VEGFB and PGF, appeared completely absent in important vertebrate clades such as birds and amphibia, respectively. In contrast, individual PDGF/VEGF gene duplications frequently occurred in fish on top of the known fish-specific whole-genome duplications. The lack of precise counterparts for human genes poses limitations but also offers opportunities for research using organisms that diverge considerably from humans. GRAPHICAL ABSTRACT: Sources for the graphical abstract: 326 MYA and older [1]; 72–240 MYA [2]; 235–65 MYA [3] [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10456-023-09874-9. |
format | Online Article Text |
id | pubmed-10328876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-103288762023-07-09 Expansion and collapse of VEGF diversity in major clades of the animal kingdom Rauniyar, Khushbu Bokharaie, Honey Jeltsch, Michael Angiogenesis Original Paper Together with the platelet-derived growth factors (PDGFs), the vascular endothelial growth factors (VEGFs) form the PDGF/VEGF subgroup among cystine knot growth factors. The evolutionary relationships within this subgroup have not been examined thoroughly to date. Here, we comprehensively analyze the PDGF/VEGF growth factors throughout all animal phyla and propose a phylogenetic tree. Vertebrate whole-genome duplications play a role in expanding PDGF/VEGF diversity, but several limited duplications are necessary to account for the temporal pattern of emergence. The phylogenetically oldest PDGF/VEGF-like growth factor likely featured a C-terminus with a BR3P signature, a hallmark of the modern-day lymphangiogenic growth factors VEGF-C and VEGF-D. Some younger VEGF genes, such as VEGFB and PGF, appeared completely absent in important vertebrate clades such as birds and amphibia, respectively. In contrast, individual PDGF/VEGF gene duplications frequently occurred in fish on top of the known fish-specific whole-genome duplications. The lack of precise counterparts for human genes poses limitations but also offers opportunities for research using organisms that diverge considerably from humans. GRAPHICAL ABSTRACT: Sources for the graphical abstract: 326 MYA and older [1]; 72–240 MYA [2]; 235–65 MYA [3] [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10456-023-09874-9. Springer Netherlands 2023-04-05 2023 /pmc/articles/PMC10328876/ /pubmed/37017884 http://dx.doi.org/10.1007/s10456-023-09874-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Rauniyar, Khushbu Bokharaie, Honey Jeltsch, Michael Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title | Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title_full | Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title_fullStr | Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title_full_unstemmed | Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title_short | Expansion and collapse of VEGF diversity in major clades of the animal kingdom |
title_sort | expansion and collapse of vegf diversity in major clades of the animal kingdom |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10328876/ https://www.ncbi.nlm.nih.gov/pubmed/37017884 http://dx.doi.org/10.1007/s10456-023-09874-9 |
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