Bone morphogenetic proteins (BMPs), members of the transforming growth fact
or beta superfamily, have been identified by their ability to induce cartil
age and bone from nonskeletal cells and have been shown to act as a ventral
morphogen in Xenopus mesoderm. We isolated a murine homeobox-containing ge
ne, distal-less 5 (mDlx5), as a BMP-inducible gene in osteoblastic MC3T3-E1
cells. Stable transfectants of MC3T3-E1 that overexpress mD1x5 mRNA showed
increase in various osteogenic markers, a fourfold increase in alkaline ph
osphatase activity, a sixfold increase in osteocalcin production, and appea
rance in mineralization of extracellular matric:, Furthermore, mDlx5 was in
duced orthotopically in mouse embryos treated with BMP-4 and in fractured b
one of adult mice. Consistent with these observations, we also found that i
njection of mD1x5 mRNA into dorsal blastomeres enhanced the ventralization
of Xenopus embryos. These findings suggest that mD1x5 is a target gene of t
he BMP signaling pathway and acts as an important regulator of both osteoge
nesis and dorsoventral patterning of embryonic axis. (C) 1999 Academic Pres
s.