Inhibition of protein kinase A phenocopies ectopic expression of hedgehog in the CNS of wild-type and cyclops mutant embryos
- Authors
- Ungar, A.R., and Moon, R.T.
- ID
- ZDB-PUB-120105-1
- Date
- 1996
- Source
- Developmental Biology 178(1): 186-191 (Journal)
- Registered Authors
- Moon, Randall T., Ungar, Anne
- Keywords
- none
- MeSH Terms
-
- Animals
- Body Patterning
- Brain/embryology*
- Brain Chemistry
- Cyclic AMP-Dependent Protein Kinases/genetics
- Cyclic AMP-Dependent Protein Kinases/physiology*
- DNA-Binding Proteins/genetics
- Extracellular Matrix Proteins
- Eye/chemistry
- Eye/embryology*
- Gene Expression Regulation, Developmental/physiology*
- Genes, Dominant
- Growth Substances*
- Hedgehog Proteins
- Mutation
- Neural Cell Adhesion Molecules/genetics
- PAX2 Transcription Factor
- Peptides*
- Phenotype
- Proteins/analysis
- Proteins/genetics*
- RNA, Messenger/analysis
- RNA, Messenger/pharmacology
- Signal Transduction/physiology
- Trans-Activators*
- Transcription Factors/genetics
- Zebrafish/embryology
- Zebrafish/genetics
- Zebrafish Proteins
- PubMed
- 8812120 Full text @ Dev. Biol.
The zebrafish hedgehog (hh) family members tiggy-winkle hedgehog (twhh) and sonic hedgehog (shh) are involved in patterning the ventral CNS and proximal eye. Using a dominant negative protein kinase A regulatory subunit mutant, we show that these hh activities are mediated by protein kinase A. The effects of dominant negative protein kinase A on pax2 expression appear to be cell nonautonomous, suggesting that cells can respond to regulation of hh signaling by modulating an additional cell–cell signaling pathway. We also investigate the potential involvement of cyclops in the hh signaling pathway and conclude that although cyclopsmutant cells can respond to hh signaling, neither hh nor dominant negative protein kinase A rescues the phenotypes associated with cyclops.