The mouse <i>Fgf8</i> gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo

TLDR

FGF family members signal locally to regulate growth and patterning in vertebrate embryos, and Fgf8 RNA localizes to key embryonic regions such as the limb bud ectoderm, primitive streak, tail bud, facial ectoderm, and midbrain–hindbrain junction, implying a regulatory role. We provide a detailed analysis of the mouse Fgf8 gene. We mapped the Fgf8 locus to distal mouse chromosome 19 and sequenced its 5′ coding region. Our analysis uncovered a new coding exon and multiple splice sites that generate at least seven distinct secreted FGF8 transcripts with different N termini, making Fgf8 the most structurally complex member of the FGF family described to date.

Abstract

ABSTRACT Evidence is accumulating that members of the FGF gene family provide signals that act locally to regulate growth and patterning in vertebrate embryos. In this report, we provide a detailed analysis of the mouse Fgf8 gene. We have mapped the Fgf8 locus to the distal region of mouse chromosome 19, and sequenced the 5′coding region of the gene. Our data identify a new coding exon, and locate multiple splice donor and splice acceptor sites that can be used to produce at least seven transcripts encoding a family of secreted FGF8 proteins with different N termini. From these results, it appears that Fgf8 is structurally the most complex member of the FGF family described to date. In the embryo, many of the regions in which Fgf8 RNA is localized are known to direct outgrowth and patterning, including the apical ectodermal ridge of the limb bud, the primitive streak and tail bud, the surface ectoderm overlying the facial primorida and the midbrain-hindbrain junction, suggesting that FGF8 may be a component of the regulatory signals that emanate from these regions.