PUBLICATION
The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation
- Authors
- Ben Abdelkhalek, H., Beckers, A., Schuster-Gossler, K., Pavlova, M.N., Burkhardt, H., Lickert, H., Rossant, J., Reinhardt, R., Schalkwyk, L.C., Müller, I., Herrmann, B.G., Ceolin, M., Rivera-Pomar, R., and Gossler, A.
- ID
- ZDB-PUB-040706-6
- Date
- 2004
- Source
- Genes & Development 18(14): 1725-1736 (Journal)
- Registered Authors
- Gossler, A.
- Keywords
- Notochord development, Not gene, homeodomain protein
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Base Sequence
- Chromosome Walking
- Chromosomes, Artificial, Bacterial
- Cloning, Molecular
- DNA Primers
- Gene Components
- Gene Expression Regulation, Developmental*
- Genes, Homeobox/genetics*
- Green Fluorescent Proteins
- Homeodomain Proteins/genetics*
- Homeodomain Proteins/metabolism
- In Situ Hybridization
- Luminescent Proteins
- Mice/embryology*
- Mice/genetics*
- Mice, Mutant Strains
- Molecular Sequence Data
- Mutation/genetics
- Notochord/embryology*
- Phylogeny
- Sequence Analysis, DNA
- Spectrum Analysis
- Tail/embryology*
- PubMed
- 15231714 Full text @ Genes & Dev.
Citation
Ben Abdelkhalek, H., Beckers, A., Schuster-Gossler, K., Pavlova, M.N., Burkhardt, H., Lickert, H., Rossant, J., Reinhardt, R., Schalkwyk, L.C., Müller, I., Herrmann, B.G., Ceolin, M., Rivera-Pomar, R., and Gossler, A. (2004) The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation. Genes & Development. 18(14):1725-1736.
Abstract
The floating head (flh) gene in zebrafish encodes a homeodomain protein, which is essential for notochord formation along the entire body axis. flh orthologs, termed Not genes, have been isolated from chick and Xenopus, but no mammalian ortholog has yet been identified. Truncate (tc) is an autosomal recessive mutation in mouse that specifically disrupts the development of the caudal notochord. Here, we demonstrate that truncate arose by a mutation in the mouse Not gene. The truncate allele (Not(tc)) contains a point mutation in the homeobox of Not that changes a conserved Phenylalanine residue in helix 1 to a Cysteine (F20C), and significantly destabilizes the homeodomain. Reversion of F20C in one allele of homozygous tc embryonic stem (ES) cells is sufficient to restore normal notochord formation in completely ES cell-derived embryos. We have generated a targeted mutation of Not by replacing most of the Not coding sequence, including the homeobox with the eGFP gene. The phenotype of Not(eGFP/eGFP), Not(eGFP/tc), and Not(tc/tc) embryos is very similar but slightly more severe in Not(eGFP/eGFP) than in Not(tc/tc) embryos. This confirms allelism of truncate and Not, and indicates that tc is not a complete null allele. Not expression is abolished in Foxa2 and T mutant embryos, suggesting that Not acts downstream of both genes during notochord development. This is in contrast to zebrafish embryos, in which flh interacts with ntl (zebrafish T) in a regulatory loop and is essential for development of the entire notochord, and suggests that different genetic control circuits act in different vertebrate species during notochord formation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping