The Brn-3 class of POU-domain transcription factors includes three gen
es in mammals which have key roles in the development of specific grou
ps of sensory neurons. Here, we have identified three avian genes whic
h correspond to the murine genes Brn-3.0, Bm-3.1, and Bm-3.2. Using an
in situ hybridization probe generic for this gene class, the earliest
detectable expression of Brn-3 in the chick is at stage 15, in placod
al and migrating precursors of the trigeminal ganglion. By stage 19, B
rn-3.0 protein is detectable in the trigeminal and vestibulocochlear g
anglia with Bm-3.0-specific antisera, and Brn-3 message expression has
extended to the dorsal root ganglia. At later stages, when condensati
on of the trigeminal ganglion is complete, Brn-3.0-immunoreactive neur
ons are concentrated in the portion of the ganglion distal to the brai
n stem. To examine the developmental origin of the Brn-3 expressing ce
lls, we combined lipophilic dye (DiI) labeling with in situ hybridizat
ion. DiI labeling of the placodal surface ectoderm and of premigratory
neural crest cells in the neural tube reveals that all, or nearly all
, of the Brn-3-expressing neurons in the trigeminal ganglia are derive
d from the sensory placodes and not from the neural crest, and thus, t
hat Brn-3 is an early marker of the placode-derived sensory neural lin
eage, (C) 1998 John Wiley & Sons, Inc.