The fibroblast growth factor receptor 3 (Fgfr3) protein is a tyrosine
kinase receptor involved in the signal transduction of various fibrobl
ast growth factors. Recent studies suggest its important role in norma
l development. In humans, mutation in Fgfr3 is responsible for growth
disorders such as achondroplasia, hypo-achondroplasia, and thanatophor
ic dysplasia. Here, we report the complete genomic organization of the
mouse Fgfr3 gene. The murine gene spans approximately 15 kb and consi
sts of 19 exons and 18 introns. One major and one minor transcription
initiation site were identified. Position +1 is located 614 nucleotide
s upstream from the ATG initiation codon. The translation initiation a
nd termination sites are located in exons 2 and 19, respectively. Five
Sp1 sites, two AP2 sites, one Zeste site, and one Krox 24 site were o
bserved in the 5'-flanking region. The Fgfr3 promoter appears to be co
ntained within a CpG island and, as is common in genes having multiple
Sp1-binding sites, lacks a TATA box. (C) 1995 Academic Press, Inc.