Targeted disruption of int-2 (fgf-3) causes developmental defects in the tail and inner ear
Article first published online: 4 FEB 2005
Copyright © 1994 Wiley-Liss, Inc.
Molecular Reproduction and Development
Volume 39, Issue 1, pages 62–68, September 1994
How to Cite
Mansour, S. L. (1994), Targeted disruption of int-2 (fgf-3) causes developmental defects in the tail and inner ear. Mol. Reprod. Dev., 39: 62–68. doi: 10.1002/mrd.1080390111
- Issue published online: 4 FEB 2005
- Article first published online: 4 FEB 2005
- Embryonic stem cells;
- Reporter gene;
- Gene targeting
The int-2 gene (also designated fgf-3) was originally identified because its transcription is activated by the nearby integration of mouse mammary tumor virus in virus-induced tumors. Molecular analyses have revealed that the int-2 gene produces at least four mRNAs, all of which encode a protein that has 40–50% amino acid sequence similarity with the fibroblast growth factors (FGFs). Int-2 gene expression is localized to a small number of discrete sites in the developing mouse, but has not been detected in any nonneoplastic adult tissue. The expression data and the amino acid sequence similarity with the FGFs suggested several potential roles for int-2 during normal development.
To evaluate these possibilities, we initiated a genetic analysis of int-2. A gene-targeting protocol was used to generate embryonic stem (ES) cells that are heterozygous for an insertion of the neor gene into the first proteincoding exon of int-2. These cells were used to establish a line of mice that carry the gene disruption. Animals that are heterozygous for the int-2neo allele are normal and fertile. Homozygous mutants survive embryonic development and can be visually identified after 12.5 days of gestation by a short, initially dorsally curled tail. This defect is potentially due to the disruption ofint-2 expression in the primitive streak/tail bud. Most of the homozygous mutants die at orsoon after birth, but several have survived to adulthood. In addition to the tail phenotype, the surviving homozygotes show, to varying extents, symptoms characteristic of innerear abnormalities. The development of these defects could be attributed to the disruption of normal int-2 expression in the hindbrain rhombomeres thought to induce inner ear development and/or the otocyst (precursor of the inner ear) itself. Other sites of int-2 expression are not affected by the mutation. Although the tail phenotype is 100% penetrant, the inner ear phenotype caused by this mutation shows reduced penetrance and variable expressivity.
A second int-2 allele was generated in ES cells by using homologous recombination to introduce a IacZ reporter gene into the int-2 locus. This allele has also been established in a line of mice. The pattern of β-galactosidase activity in carriers of the int-2lacZ allele has been examined in embryos from 8.5–14.5 days of gestation and in neonatal heads using whole mount X-gal staining. Expression of the lacZ gene mirrors the expected pattern of int-2 mRNA. Several new sites int-2 of expression not identified in the initial in situ hybridization studies of int-2 mRNA have also been identified. Compound heterozygotes (int-2neo/int-2lacZ) were found to have the same defects in tail and innerear development as homozygous int-2neo mice. After staining for β-galactosidase activity, these mutants should allow an analysis of the int-2 mutant phenotype at the cellular level. © 1994 Wiley-Liss, Inc.