Fig. 5. ß-galactosidase staining of mammillary body axonal projections in
E14.5 Sim1/Sim2 mutant embryos. E14.5 brains of various genotypes
were stained for ß-galactosidase activity and sectioned coronally. For
each brain, four consecutive sections are shown, the most anterior being at
the top of the figure. PMTs are indicated by arrows, whereas the abnormally
targeted axons are indicated by arrowheads. The loss of Sim1 function
is associated with a decrease of the PMT and the emergence of MB axons
directed towards the midline. Sim2 also contributes to this
phenotype, as the axonal abnormalities are more severe in
Sim1tlz/tlz;Sim2-/- than in
Sim1tlz/tlz;Sim2+/+ embryos.