PUBLICATION
Expression of three spalt (sal) gene homologues in zebrafish embryos
- Authors
- Camp, E., Hope, R., Kortschak, R.D., Cox, T.C., and Lardelli, M.
- ID
- ZDB-PUB-030304-15
- Date
- 2003
- Source
- Development genes and evolution 213(1): 35-43 (Journal)
- Registered Authors
- Camp, Esther, Cox, Tony, Kortschak, Daniel, Lardelli, Michael
- Keywords
- none
- MeSH Terms
-
- Animals
- Base Sequence
- Evolution, Molecular
- Gene Expression Profiling
- Gene Expression Regulation, Developmental/genetics*
- Homeodomain Proteins/genetics*
- Markov Chains
- Molecular Sequence Data
- Monte Carlo Method
- Phylogeny*
- Sequence Alignment
- Sequence Homology
- Transcription Factors/genetics*
- Xenopus Proteins*
- Zebrafish/embryology*
- Zebrafish/genetics*
- PubMed
- 12590351 Full text @ Dev. Genes Evol.
Citation
Camp, E., Hope, R., Kortschak, R.D., Cox, T.C., and Lardelli, M. (2003) Expression of three spalt (sal) gene homologues in zebrafish embryos. Development genes and evolution. 213(1):35-43.
Abstract
Three homologues of the Drosophilaregion-specific homeotic gene spalt( sal) have been isolated in zebrafish, sall1a, sall1b and sall3. Phylogenetic analysis of these genes against known salDNA sequences showed zebrafish sall1aand sall1b to be orthologous to other vertebrate sal-1 genes and zebrafish sall3to be orthologous to other vertebrate sal-3 genes, except Xenopus sall3. Phylogenetic reconstruction suggests that zebrafish sall1a and sall1bresulted from a gene duplication event occurring prior to the divergence of the ray-finned and lobe-finned fish lineages. Analysis of the expression pattern of the zebrafish sal genes shows that sall1a and sall3 share expression domains with both orthologous and non-orthologous vertebrate sal genes. Both are expressed in various regions of the CNS, including in primary motor neurons. Outside of the CNS, sall1a expression is observed in the otic vesicle (ear), heart and in a discrete region of the pronephric ducts. These analyses indicate that orthologies between zebrafish sal genes and other vertebrate sal genes do not imply equivalence of expression pattern and, therefore, that biological functions are not entirely conserved. However we suggest that, like other vertebrate sal genes, zebrafish sal genes have a role in neural development. Also, expression of zebrafish sall1a in the otic vesicle, heart sac and the pronephric ducts of zebrafish embryos is possibly consistent with some of the abnormalities seen in Sall1-deficient mice and in Townes-Brocks Syndrome, a human disorder which is caused by mutations in the human spalt gene SALL1.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping