PUBLICATION
Prmt5 promotes vascular morphogenesis independently of its methyltransferase activity
- Authors
- Quillien, A., Gilbert, G., Boulet, M., Ethuin, S., Waltzer, L., Vandel, L.
- ID
- ZDB-PUB-210622-52
- Date
- 2021
- Source
- PLoS Genetics 17: e1009641 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Base Sequence
- Chromatin/chemistry
- Chromatin/metabolism
- Embryo, Nonmammalian
- Endothelial Cells/cytology
- Endothelial Cells/metabolism
- Gene Expression Regulation, Developmental*
- Hematopoiesis/genetics*
- Morphogenesis/genetics*
- Mutation
- Neovascularization, Physiologic/genetics*
- Protein Isoforms/genetics
- Protein Isoforms/metabolism
- Protein-Arginine N-Methyltransferases/genetics*
- Protein-Arginine N-Methyltransferases/metabolism
- Proto-Oncogene Proteins c-ets/genetics*
- Proto-Oncogene Proteins c-ets/metabolism
- Signal Transduction
- Transcription, Genetic
- Zebrafish/genetics*
- Zebrafish/growth & development
- Zebrafish/metabolism
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- PubMed
- 34153034 Full text @ PLoS Genet.
Citation
Quillien, A., Gilbert, G., Boulet, M., Ethuin, S., Waltzer, L., Vandel, L. (2021) Prmt5 promotes vascular morphogenesis independently of its methyltransferase activity. PLoS Genetics. 17:e1009641.
Abstract
During development, the vertebrate vasculature undergoes major growth and remodeling. While the transcriptional cascade underlying blood vessel formation starts to be better characterized, little is known concerning the role and mode of action of epigenetic enzymes during this process. Here, we explored the role of the Protein Arginine Methyl Transferase Prmt5 in blood vessel formation as well as hematopoiesis using zebrafish as a model system. Through the combination of different prmt5 loss-of-function approaches we highlighted a key role of Prmt5 in both processes. Notably, we showed that Prmt5 promotes vascular morphogenesis through the transcriptional control of ETS transcription factors and adhesion proteins in endothelial cells. Interestingly, using a catalytic dead mutant of Prmt5 and a specific drug inhibitor, we found that while Prmt5 methyltransferase activity was required for blood cell formation, it was dispensable for vessel formation. Analyses of chromatin architecture impact on reporter genes expression and chromatin immunoprecipitation experiments led us to propose that Prmt5 regulates transcription by acting as a scaffold protein that facilitates chromatin looping to promote vascular morphogenesis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping