PUBLICATION
Identification and spatiotemporal expression of gpr161 genes in zebrafish
- Authors
- Wang, M., Li, P., Wang, H., Dong, L., Wu, C., Zhao, Z.
- ID
- ZDB-PUB-191231-15
- Date
- 2019
- Source
- Gene 730: 144303 (Other)
- Registered Authors
- Wang, Hao, Zhao, Zhonghua
- Keywords
- Hh signaling pathway, adaxial cell, central nervous system (CNS), gpr161, posterior blood island (PBI), zebrafish
- MeSH Terms
-
- Animals
- Central Nervous System/metabolism
- Databases, Genetic
- Embryonic Development/genetics
- Gene Expression Regulation, Developmental/genetics
- Humans
- Mice
- Phylogeny
- Receptors, G-Protein-Coupled/genetics*
- Receptors, G-Protein-Coupled/metabolism*
- Sequence Alignment
- Sequence Analysis, DNA
- Wnt Signaling Pathway/genetics
- Zebrafish/genetics
- Zebrafish Proteins/genetics
- PubMed
- 31884103 Full text @ Gene
Citation
Wang, M., Li, P., Wang, H., Dong, L., Wu, C., Zhao, Z. (2019) Identification and spatiotemporal expression of gpr161 genes in zebrafish. Gene. 730:144303.
Abstract
G protein coupled Receptor 161 (GPR161) is a ciliary orphan GPCR. It is reported to play critical roles in regulating vertebrate Hedgehog (Hh) signaling pathway, that is conserved in metazoan and functions in earlier embryogenesis and homeostasis of adult metabolism. However, to date, all GPR161 functional studies were performed only in mouse. Knock out gpr161 in NIH3T3 cell lines, the common material for Hh mechanism research, failed to give any obvious Hh pathway defects, raising the question that whether GPR161 functions in Hh pathway is conserved in vertebrate system. Here, we described the characterization and spatiotemporal expression of two zebrafish gpr161 homologs, gpr161a and gpr161b. gpr161a was renamed of the gpr161 previously identified, while gpr161b was novel identified. The whole-mount in situ hybridization and quantitative PCR results showed that gpr161a is initially expressed in maternal manner while gpr161b is not. Although these two gpr161 showed ubiquitously expressed at early embryonic stages, each of them had tissue specific accumulation. gpr161a is abundant in the central nervous system (CNS) and adaxial cells, where are rich of Hh responding cells. Together gpr161a was highly expressed in muscle and intestine in adult fishes. These results strongly suggest the regulating roles of Gpr161 a in zebrafish Hh signal transduction. gpr161b was also accumulated in the CNS but mainly at the midline in the neural tube, similar pattern as wnt5b expression in such area, suggesting its potential function correlated with WNT signaling pathway. Interestingly, we also found the specific accumulation of gpr161 in posterior blood island (PBI) at 24 hours post fertilization (hpf), indicating the gpr161 may play roles in early hematopoiesis in zebrafish. Our work provides a starting point to unveil the divergent functions of gpr161 in vertebrate and will shed light on the studies of mechanism of Hh and WNT pathways, as well as early hematopoiesis.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping