PUBLICATION
nemo-like kinase is an essential co-activator of Wnt signaling during early zebrafish development
- Authors
- Thorpe, C.J., and Moon, R.T.
- ID
- ZDB-PUB-040521-6
- Date
- 2004
- Source
- Development (Cambridge, England) 131(12): 2899-2909 (Journal)
- Registered Authors
- Moon, Randall T., Thorpe, Chris
- Keywords
- Nemo-like kinase, Wnt, Zebrafish, Tcf, Lef
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Body Patterning/physiology*
- Brain/embryology*
- Conserved Sequence
- Ectoderm/physiology
- Embryo, Nonmammalian/physiology
- Gastrula/physiology
- Gene Expression Regulation, Developmental/genetics*
- Gene Expression Regulation, Enzymologic/genetics
- In Situ Hybridization
- Mitogen-Activated Protein Kinases/genetics*
- Mitogen-Activated Protein Kinases/metabolism*
- Molecular Sequence Data
- Morphogenesis
- Nervous System/embryology
- Polymerase Chain Reaction
- Proto-Oncogene Proteins/physiology*
- Sequence Alignment
- Sequence Homology, Amino Acid
- Wnt Proteins
- Zebrafish/embryology*
- Zebrafish Proteins*
- PubMed
- 15151990 Full text @ Development
Citation
Thorpe, C.J., and Moon, R.T. (2004) nemo-like kinase is an essential co-activator of Wnt signaling during early zebrafish development. Development (Cambridge, England). 131(12):2899-2909.
Abstract
Wnt/beta-catenin signaling regulates many aspects of early vertebrate development, including patterning of the mesoderm and neurectoderm during gastrulation. In zebrafish, Wnt signaling overcomes basal repression in the prospective caudal neurectoderm by Tcf homologs that act as inhibitors of Wnt target genes. The vertebrate homolog of Drosophila nemo, nemo-like kinase (Nlk), can phosphorylate Tcf/Lef proteins and inhibit the DNA-binding ability of beta-catenin/Tcf complexes, thereby blocking activation of Wnt targets. By contrast, mutations in a C. elegans homolog show that Nlk is required to activate Wnt targets that are constitutively repressed by Tcf. We show that overexpressed zebrafish nlk, in concert with wnt8, can downregulate two tcf3 homologs, tcf3a and tcf3b, that repress Wnt targets during neurectodermal patterning. Inhibition of nlk using morpholino oligos reveals essential roles in regulating ventrolateral mesoderm formation in conjunction with wnt8, and in patterning of the midbrain, possibly functioning with wnt8b. In both instances, nlk appears to function as a positive regulator of Wnt signaling. Additionally, nlk strongly enhances convergent/extension phenotypes associated with wnt11/silberblick, suggesting a role in modulating cell movements as well as cell fate.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping