Little is currently known regarding the ontogeny of smooth muscle tiss
ues during normal mammalian development. The a-smooth muscle and gamma
-smooth muscle isoactins have been shown to be excellent molecular mar
kers of smooth muscle cell phenotype. This study characterizes both th
e temporal and spatial patterns of or-smooth muscle and gamma-smooth m
uscle isoactin expression in the developing mouse. In situ analysis wa
s performed on serial sections of whole mouse embryos on embryonic day
9, 11, 13, 15, and 17 using alpha-smooth muscle and gamma-smooth musc
le isoactin-specific riboprobes. Distinct temporal and spatial pattern
s of a-smooth muscle and gamma-smooth muscle isoactin gene expression
were observed in the developing gastrointestinal tract, urogenital tra
ct, respiratory tract, and vascular system. Independent expression of
the or-smooth muscle isoactin was observed during the early stages of
skeletal, cardiac, and smooth muscle myogenesis as well as in a novel
subset of distinct organs including the postanal component of the hind
gut, allantois, and primitive placenta. The results of this study indi
cate that distinct cellular phenotypes are involved in smooth muscle m
yogenesis and suggest that organ-specific mechanisms might exist for t
he initiation of smooth muscle development in vivo. In addition, the p
attern of independent or-smooth muscle isoactin expression observed in
this study provides novel information regarding the early stages of h
indgut and placental development, and suggests that a common functiona
l phenotype may be associated with the early stages of skeletal, cardi
ac, and smooth muscle myogenesis. (C) 1995 Wiley-Liss, Inc.