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Fig. 2. Ventral cell types are lost in FGFR double mutants. RNA in situ
hybridization analysis of E12.5 coronal brain sections using radioactive
probes. (A,E,I) In the control embryo, expression of
Pax6 (A), Dlx2 (E) and Nkx2.1 (I) are used to
identify the dorsal, ventral and ventromedial areas of the telencephalon.
(B,F,J) In the
Fgfr2-/-;Fgfr3-/- mutant, dorsoventral
patterning and morphology of the telencephalon are grossly normal.
(C,G,K) In the
Fgfr1-/-;Fgfr3-/- mutant, although the
borders of expression of Pax6 (C), Dlx2 (G) and Nkx2.1 (K) are normal
(arrowheads), indicating proper dorsoventral specification of precursor cells,
the morphology of the ventral telencephalon is abnormal and flattened in
appearance. (D,H,L)In the
Fgfr1-/-;Fgfr2-/- mutant, ventral
precursor cells are lost, indicated by expression of Pax6 that
extends to the ventral midline (D) and by the loss of Dlx2 (H) and
Nkx2.1 (L) expression.