Genetic Evidence for a Noncanonical Function of Seryl-tRNA Synthetase in Vascular Development
- Herzog, W., Müller, K., Huisken, J., and Stainier, D.Y.
- Circulation research 104(11): 1260-1266 (Journal)
- Registered Authors
- Herzog, Wiebke, Stainier, Didier
- aminoacyl-tRNA synthetases, seryl-tRNA synthetase, Sars, SerRS, zebrafish, angiogenesis, vascular dilatation
- MeSH Terms
- Angiogenesis Inhibitors/pharmacology
- Aorta, Thoracic/cytology
- Aorta, Thoracic/embryology
- Aorta, Thoracic/physiology
- Cell Division
- Cerebrovascular Circulation/physiology*
- Chromosome Mapping
- Embryo, Nonmammalian/physiology
- Endothelium, Vascular/cytology
- Endothelium, Vascular/physiology
- RNA, Small Interfering/genetics
- Serine-tRNA Ligase/genetics*
- Umbilical Veins/cytology
- Umbilical Veins/physiology
- 19423847 Full text @ Circ. Res.
Herzog, W., Müller, K., Huisken, J., and Stainier, D.Y. (2009) Genetic Evidence for a Noncanonical Function of Seryl-tRNA Synthetase in Vascular Development. Circulation research. 104(11):1260-1266.
In a recent genetic screen, we identified mutations in genes important for vascular development and maintenance in zebrafish (Jin et al. Dev Biol. 2007;307:29-42). 32 Mutations at the adrasteia (adr) locus cause a pronounced dilatation of the aortic arch vessels as well as aberrant patterning of the hindbrain capillaries and, to a lesser extent, intersomitic vessels. This dilatation of the aortic arch vessels does not appear to be caused by increased cell proliferation but is dependent on vascular endothelial growth factor (Vegf) signaling. By positional cloning, we isolated seryl-tRNA synthetase (sars) as the gene affected by the adr mutations. Small interfering RNA knockdown experiments in human umbilical vein endothelial cell cultures indicate that SARS also regulates endothelial sprouting. These analyses of zebrafish and human endothelial cells reveal a new noncanonical function of Sars in endothelial development.
Genes / Markers
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes