Terminal portions of the Drosophila body pattern are specified by an e
xtracellular ligand generated at each end of the early syn-cytial embr
yo. This ligand triggers the localized transcription of two gap segmen
tation genes, tailless (tll) and huckebein (hkb) through a signal tran
sduction cascade involving the receptor tyrosine kinase torso (tor) an
d homologues of ras, raf, and mek (map kinae kinase). In contrast to t
he ligand, these signal transducing components are expressed ubiquitou
sly. Here, we show that a constitutively active form of human raf1 pro
tein can trigger tll and hkb transcription in Drosophila embryos and s
pecify elements of the terminal body pattern. This result indicates a
strong functional conservation between Drosophila and mammalian raf pr
oteins and argues that the localized activity of Drosophila raf (D-raf
) normally carries spatial information specifying the end portions of
the body.