We describe the molecular characterization of the paired-type homeobox
gene D-Ptx1 of Drosophila, a close homolog of the mouse pituitary hom
eobox gene Ptx1 and the unc-30 gene of C. elegans, characterized by a
lysine residue at position 9 of the third alpha-helix of the homeodoma
in. D-Ptx1 is expressed at various restricted locations throughout emb
ryogenesis. Initial expression of D-Ptx1 in the posterior-most region
of the blastoderm embryo is controlled by fork head activity in respon
se to the activated Ras/Raf signaling pathway. During later stages of
embryonic development, D-Ptx1 transcripts and protein accumulate in th
e posterior portion of the midgut, in the developing Malpighian tubule
s, in a subset of ventral somatic muscles, and in neural cells. Phenot
ypic analysis of gain-of-function and lack-of-function mutant embryos
show that the D-Ptxl gene is not involved in morphologically apparent
differentiation processes. We conclude that D-Ptx1 is more likely to c
ontrol physiological cell functions than pattern formation during Dros
ophila embryogenesis. (C) 1997 Elsevier Science Ireland Ltd.