Project Details
Description
The FGF-5 proto-oncogene specifies a secreted growth factor which bears
sequence homology to the prototypic fibroblast growth factors. FGF-5. is
expressed in several embryonic settings, in mature brain, and in some
neoplastic cells. This application proposes a series of genetic experiments
to determine many of FGF-5's distinct functions. We shall disrupt one or
both alleles of the FGF-5 gene in murine totipotent embryonic stem (ES)
cells by homologous recombination. FGF-5 negative ES cells will be analyzed
for differentiation potential as embryoid bodies in vitro and as tumors in
vivo. FGF-5 hemizygous ES cells will be injected into blastocysts to derive
chimeric mice and establish a disrupted allele in the germ line. Inbreeding
will be performed to determine the developmental abnormalities in FGF-5
negative embryos. We shall also establish transgenic mice bearing human
FGF-5 genes which are expressed in a subset of the developmentally
characteristic sites or which bear structural mutations in a domain of
currently unknown function. Mating these transgenic strains with FGF-5
hemizygous mice and backcrossing progeny with the hemizygous strain will
generate embryos carrying the transgenes as sole functional allele. The
aberrant phenotypes of these embryos will further dissect FGF-5 function.
Lastly, we shall generate mice carrying human FGF-5 transgenes mutated at
sites known to increase the translation efficiency of FGF-5 MRNA. These
mice should overexpress FGF-5 protein without ectopic expression, and
resulting abnormalities will also help determine FGF-5 function. These mice
shall also be monitored for cancer predisposition.
Status | Finished |
---|---|
Effective start/end date | 8/1/90 → 7/31/93 |
Funding
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development
ASJC Scopus Subject Areas
- Genetics
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