PUBLICATION
Urp1 and Urp2 act redundantly to maintain spine shape in zebrafish larvae
- Authors
- Gaillard, A.L., Mohamad, T., Quan, F.B., de Cian, A., Mosimann, C., Tostivint, H., Pézeron, G.
- ID
- ZDB-PUB-230204-19
- Date
- 2023
- Source
- Developmental Biology 496: 36-51 (Journal)
- Registered Authors
- Gaillard, Anne Laure, Mosimann, Christian, Pézeron, Guillaume, Tostivint, Hervé
- Keywords
- Spine, Urotensin 2, Urp, Zebrafish
- MeSH Terms
-
- Animals
- Larva
- Morphogenesis
- Neuropeptides*
- Spine
- Zebrafish*
- Zebrafish Proteins
- PubMed
- 36736605 Full text @ Dev. Biol.
Citation
Gaillard, A.L., Mohamad, T., Quan, F.B., de Cian, A., Mosimann, C., Tostivint, H., Pézeron, G. (2023) Urp1 and Urp2 act redundantly to maintain spine shape in zebrafish larvae. Developmental Biology. 496:36-51.
Abstract
Urp1 and Urp2 are two neuropeptides, members of the Urotensin 2 family, that have been recently involved in the control of body axis morphogenesis in zebrafish. They are produced by a population of sensory spinal neurons, called cerebrospinal fluid contacting neurons (CSF-cNs), under the control of signals relying on the Reissner fiber, an extracellular thread bathing in the CSF. Here, we have investigated further the function of Urp1 and Urp2 (Urp1/2) in body axis formation and maintenance. We showed that urp1;urp2 double mutants develop strong body axis defects during larval growth, revealing the redundancy between the two neuropeptides. These defects were similar to those previously reported in uts2r3 mutants. We observed that this phenotype is not associated with congenital defects in vertebrae formation, but by using specific inhibitors, we found that, at least in the embryo, the action of Upr1/2 signaling depends on myosin II contraction. Finally, we provide evidence that while the Urp1/2 signaling is functioning during larval growth, it is dispensable for embryonic development. Taken together, our results show that Urp1/2 signaling is required in larvae to promote correct vertebral body axis, most likely by regulating muscle tone.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping