Altered timing of the extracellular-matrix-mediated epithelial-mesenchymalinteraction that initiates mandibular skeletogenesis in three inbred strains of mice: Development, heterochrony, and evolutionary change in morphology
Me. Macdonald et Bk. Hall, Altered timing of the extracellular-matrix-mediated epithelial-mesenchymalinteraction that initiates mandibular skeletogenesis in three inbred strains of mice: Development, heterochrony, and evolutionary change in morphology, J EXP ZOOL, 291(3), 2001, pp. 258-273
Subtle changes in embryonic development are a source of significant morphol
ogical alterations during evolution. The mammalian mandibular skeleton, whi
ch originates from the cranial neural crest, is a complex structure compris
ing several components that interact late in embryogenesis to produce a sin
gle functional unit. It provides a model system in which individual develop
mental events at the basis of population-level evolutionary change can be i
nvestigated experimentally. Inbred mouse strains exhibit obvious morphologi
cal differences despite the relatively short time since their divergence fr
om one another. Some of these differences can be traced to small changes in
the timing of early developmental events such as the formation of the cell
ular condensations that initiate skeletogenesis. This paper examines an eve
n earlier event for changes in timing, the epithelial-mesenchymal interacti
on(s) required to initiate chondrogenesis of Meckel's cartilage and osteoge
nesis of the dentary bone. Using three inbred strains of mice (CBA, C3H and
C57) we found that, within each strain, cartilage and bone are induced at
the same time and by the same (mandibular) epithelium, that chondrogenesis
and osteogenesis are initiated by a matrix-mediated epithelial-mesenchymal
interaction, and that timing of the interactions differs among the three in
bred strains. These results are discussed with respect to the possible mole
cular basis of such temporal shifts in inductive interactions and how such
studies can be used to shed light on heterochrony as a mechanism of evoluti
onary change in morphology. (C) 2001 Wiley-Liss, Inc.