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Fig. 1. Morphogenetic movement defects in developing mouse eyes deficient for RA
synthesis. (A-D) Hematoxylin and eosin staining of frontal sections
through the eye of E14.5 wild-type (WT), Raldh1-/-
(R1-/-), Raldh3-/- (R3-/-) and
Raldh1-/-;Raldh3-/- double null
(R1;R3-/-) embryos. The double-arrow indicates thickening of
the neural retina in R3-/- and R1;R3-/- embryos; notice the
lack of a vitreous body and the presence of a retrolenticular membrane in
these mutants. (E-H) Expression of RARE-lacZ (an RA-reporter
transgene) in whole-mount E10.5 wild-type and mutant embryos. Note the near
complete loss of RARE-lacZ expression in eyes of
R1;R3-/- embryos. Olfactory pit staining is completely
dependent upon Raldh3, but forebrain staining is not dependent upon
Raldh1 or Raldh3. c, cornea; D, dorsal; e, eye; el, eyelid;
f, forebrain; olf, olfactory pit; pm, perioptic mesenchyme; rlm,
retrolenticular membrane; V, ventral; vb, vitreous body.