The mouse cerebellar cortex is subdivided by an elaborate array of parasagi
ttal and transverse boundaries. The relationship between these two orthogon
al patterns of compartmentation is understood poorly. We have combined the
use of adult and perinatal molecular markers of compartmentation-zebrin II,
calbindin, and an L7/pcp-2-lacZ transgene-to resolve some of these issues.
Our results indicate that the adult cerebellar vermis is divided along the
rostrocaudal axis by three transverse boundaries: through the rostral face
of lobule VI, in the caudal half of lobule VII, and across the posterolate
ral fissure between lobules IX and X. These three boundaries subdivide the
vermis into four transverse zones: the anterior zone (lobules I-V), the cen
tral zone (lobules VI-VII), the posterior zone (lobules VIII-IX), and the n
odular zone (lobule X). The same zones and boundaries also can be identifie
d in the newborn cerebellum. The parasagittal organization is different in
each zone: a unique combination of Purkinje cell phenotypes is found in eac
h transverse zone both in the neonate and the adult, and different zones ha
ve distinct developmental time tables. Furthermore, the parasagittal bands
of Purkinje cells revealed in the adult cerebellar cortex by using antizebr
in II immunocytochemistry are discontinuous across the transverse boundarie
s. These data suggest that the transverse zones of the vermis form first du
ring development and that parasagittal compartmentation develops independen
tly in each transverse zone. (C) 1999 Wiley-Liss, Inc.