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Fig. 6. Expression of DLX1, DLX2 and BRN3b in the ocular retardation
(orJ/orJ) mouse. (A-C) OrJ/orJ
mutants (Chx10 null) lack expression of BRN3b (A), DLX1 (B) and DLX2
(C) at E13.5, indicating absent RGCs. (D-F)Wild-type controls exhibit normal
patterns of expression of these markers. By E16.5, there are BRN3b-expressing
cells in orJ/orJ mutants (G). BRN3b expression coincides
with the onset of DLX1 and DLX2 expression (H, DLX1; I, DLX2). (J-L)
Expression in controls (J, BRN3b; K, DLX1; L, DLX2). By E18.5, BRN3b
expression is localized in the central inner retina in both
orJ/orJ mutants and controls (M, mutant; P, wild type).
DLX1 expression is not detected (N, mutant; Q, wild type) at E18.5. DLX2
expression is found in the inner and outer retina in both mutants and wild
types (O, mutant; R, wild-type). The expression pattern of DLX2 is
considerably disorganized in the orJ/orJ mutant compared
with wild-type controls at this stage (O,R). Scale bars: 100 µm in F; 50
µm in L; 50 µm in R.