Fig. 2. Expression of Tau-reporters mimic endogenous O/E pattern. (A,C)
Mid-sagittal view of an adult O/E2 heterozygous animal after X-gal
staining. ß-galactosidase activity was present in the olfactory
epithelium and bulb (A), vomeronasal organ (C) and axon fibers projecting from
these two structures. (B,D) Mid-sagittal view of an adult O/E3
heterozygous animal. GFP fluorescence was visible in the olfactory epithelium
and bulb (B), vomeronasal organ (D), and axon fibers projecting from these two
structures. (E) X-gal staining of olfactory epithelium section of an
O/E2lacZ/lacZ animal showing ß-gal activity in the
ORN cell bodies and axon bundles. (F) X-gal staining of OB section of
O/E2lacZ/+ animal showing ß-gal activity in ORN axons
projecting to the olfactory glomeruli. (G) An olfactory epithelium section of
an O/E3GFP/+ animal showing GFP fluorescence in the ORN
cell bodies and axon bundles. (H) An OB section of
O/E3GFP/+ animal showing GFP fluorescence in ORN axons
projecting to the olfactory glomeruli. (I,J) Whole-mount X-gal staining of an
E11 O/E2lacZ/+ mouse embryo showing ß-gal expression
in the neural tissues. (K) Two-color confocal image of OE from heterozygous
OE3 mouse. Intrinsic GFP localization is shown in green and neuronal specific
tubulin shown in red. Two cells near the basal lamina that express only the
GFP reporter are indicated by arrows.