Mk. Duncan et al., EXPRESSION OF THE HELIX-LOOP-HELIX GENES ID-1 AND NSCL-1 DURING CEREBELLAR DEVELOPMENT, Developmental dynamics, 208(1), 1997, pp. 107-114
Neurons throughout the central nervous system (CNS) undergo proliferat
ion, migration, and differentiation during their histogenesis. Althoug
h numerous regulatory molecules are expressed in developing neurons, i
t is unknown whether most of these molecules have the same function th
roughout the CNS or play different roles in different neuronal populat
ions. Previous studies have shown that Id-1 and NSCL-1 are expressed a
t high levels in the ventricular and subependymal zones, respectively,
of the embryonic brain. In the present study, the expression of Id-1
and NSCL-1 was further investigated during postnatal development of th
e cerebellum. By Northern blot hybridization analysis, the expression
levels of Id-1 and NSCL-1 mRNA were developmentally regulated in the c
erebellum, with the highest mRNA levels coinciding with the time of ma
ximal granule cell histogenesis. By in situ hybridization, NSCL-1 mRNA
was found in the premigratory zone of the external granule layer (EGL
), a structure developmentally analogous to the subependymal zone of t
he embryonic brain. In normal mice, Id-1 mRNA was found to be transien
tly expressed in the upper internal granule layer (IGL), a population
of cells that recently completed their migration from the EGL. In the
mouse mutant weaver, Id mRNA was only seen in granule cells that have
reached their normal positions in the IGL. No Id-1 hybridization signa
l was observed in the large numbers of granule cells remaining in the
EGL of weaver mice, indicating that Id-1 expression is controlled by s
patial cues. The lack of Id-1 expression in ectopic weaver granule cel
ls is compatible with previous suggestions of arrested differentiation
. These results support the idea that transcriptional regulators of th
e helix-loop-helix gene family play important roles in neuronal develo
pment, exhibiting region-specific expression and function. (C) 1997 Wi
ley-Liss, Inc.