HOX11, a human homeobox gene with putative oncogenic potential, was or
iginally discovered at the chromosome 10 breakpoint in T-cell acute ly
mphoblastic leukemias bearing the chromosomal translocation t(10;14)(q
24;q11). To provide insight into the possible roles of this gene in de
velopment, we isolated and characterized its murine homolog, Tlx-1, an
d examined its profile of expression. Tlx-1 transcripts are first dete
cted at E8.5 in the surface ectoderm and central mesenchyme of the fir
st branchial arch. This expression subsequently extends to the 2nd, 3r
d, and 4th branchial arches, as well as the presumptive pharynx, as th
ese structures develop. Between E12.5 and E15.5, the profile of Tlx-1
expression becomes more complex; expression is observed in the develop
ing pancreas and salivary glands, as well as in several components of
the nervous system, including the trigeminal, glossopharyngeal and ves
tibulocochlear ganglia, the spinal cord, and the curvature of the pons
-medulla. In addition, expression is seen in the pinna and external au
ditory meatus of the outer ear, the tooth primordia, and specific cell
populations of the mandible and tongue. These complex patterns of exp
ression are consistent with multiple and varied roles for Tlx-1 in dev
elopment and suggest that Tlx-l marks, amongst other cell populations,
structures derived from cranial neural crest cells and migratory para
xial mesoderm that arise at corresponding levels along the rostral-cau
dal axis of the developing embryo.