Hb. Wood et al., EFFECTS OF ALL-TRANS-RETINOIC ACID ON SKELETAL PATTERN, 5'HOXD GENE-EXPRESSION, AND RAR-BETA-2 BETA-4 PROMOTER ACTIVITY IN EMBRYONIC MOUSE LIMBS/, Developmental genetics, 19(1), 1996, pp. 74-84
Mouse embryos were exposed to all-trans-retinoic acid on day 11 or day
12 of development and the resulting skeletal pattern alterations comp
ared with early effects on Hoxd-11 and Hoxd-13 expression domains and
RAR-beta 2/beta 4 promoter activity. The effects on skeletal pattern s
howed a clear correlation between the timing of retinoic acid exposure
and the sequence of mesenchymal condensation. Ectopic RAR-beta 2/beta
4 promoter activity was detected within 2 hr of exposure to retinoic
acid, and was present throughout the limb bud after 5 hr; it remained
high in the apical ectodermal ridge and proximal mesenchyme after 12 h
r, by which time the abnormal digital pattern could be seen. HoxD gene
expression domains in the distal handplate were narrowed by 5 hr afte
r maternal retinoic acid administration on day 11. Following retinoic
acid treatment on both day 11 and day 12, the normal downregulation of
Hoxd-11 and Hoxd-13 in the digital mesenchymal condensations was reta
rded. There was no evidence to suggest that RAR-beta 2/beta 4 promoter
activity mediates the effects of RA on HoxD gene expression, but ecto
pic promoter activity is a useful indicator of at least some of the si
tes in which RA levels are raised. We suggest (1) that the apical ecto
dermal ridge is the most functionally significant of these sites, (2)
that raised retinoic acid levels in the ridge result in altered gene e
xpression and/or altered cell proliferation within this epithelium, (3
) that both altered HoxD ene expression domains and altered skeletal p
attern formation are secondary to this effect. There was a good correl
ation between the effects of retinoic acid on Hoxd-11 and Hoxd-13 expr
ession and delay of skeletal differentiation, suggesting that this may
be a direct effect. (C) 1996 Wiley-Liss, Inc.