The specific properties of mineralized tissues are defined by the comp
osition of the fraction of the noncollagenous matrix proteins, Because
these proteins play a pivotal role in the processes of cell different
iation and activation and of mineralization, their temporal and spatia
l expression is tightly regulated, Within this study, the expression o
f the enamel protein amelogenin and of the bone matrix proteins osteop
ontin, bone sialoprotein, osteocalcin, and osteonectin was investigate
d by in situ hybridization. Two models that allow observation of the f
ormation of mineralized tissues were chosen, The development of bone a
nd cartilage was observed on murine metatarsals from W-day-old embryos
up to I-day-old mice, This time covers the periods of initial bone fo
rmation as well as onset of resorption of mineralized cartilage and bo
ne, To study gene expression in the mineralized tissues of the dental
organ, enamel, dentin, and cementum, developing molars ranging in age
from 16-day-old embryos to 14 days after delivery were chosen, Within
this time frame, the molars develop from an immature state to the diff
erentiated organ which erupts through the mandibular bone. In the deve
loping metatarsals, osteopontin and bone sialoprotein mRNAs were detec
ted in osteoblasts and hypertrophic chondrocytes at the onset of miner
alization, In the tooth organ, only cementoblasts expressed transcript
s encoding the two proteins; odontoblasts and ameloblasts did not expr
ess these genes, Osteonectin was expressed by osteoblasts and hypertro
phic chondrocytes as well, whereas in the molars it was produced exclu
sively by odontoblasts, Osteocalcin was expressed specifically by oste
oblasts in the developing metatarsals. In tooth, osteocalcin transcrip
ts were detected in odontoblasts. Finally, amelogenin was a specific p
roduct of ameloblasts, Thus, a sequential and cell type-restricted exp
ression of matrix proteins takes place during the development of the m
ineralized tissues, The expression patterns of the transcripts encodin
g the bone matrix proteins suggest different biological roles dependin
g on the time and site of expression.