Ge. Lyons et al., PROTOONCOGENE C-SKI IS EXPRESSED IN BOTH PROLIFERATING AND POSTMITOTIC NEURONAL POPULATIONS, Developmental dynamics, 201(4), 1994, pp. 354-365
The cellular protooncogene, c-ski, is expressed in all cells of the de
veloping mouse at low but detectable levels. In situ hybridization and
Northern blot analyses reveal that some cells and tissues express thi
s gene at higher levels at certain stages of embryonic and postnatal d
evelopment. RT-PCR results indicate that alternative splicing of exon
2, known to occur in chickens (Sutrave and Hughes [1989] Mel. Cell. Bi
ol, 9:4046-4051; Grimes et al. [1993] Oncogene 8:2863-2868) does not o
ccur in adult mouse tissues. In the embryo, neural crest cells express
the c-ski gene during migration at 8.5 to 9.5 days post coitum (p.c.)
. Neural crest derivatives such as dorsal root ganglia and melanocytes
stain positively with an antibody to the ski protein. At 9 days p.c.,
the entire neural tube has high levels of c-ski gene expression. By 1
2-13.5 days only the ependymal layer expresses c-ski above background
levels. At 14-16 days p.c., c-ski mRNAs are detected at high levels in
the cortical layers of the brain and in the olfactory bulb, In 2 week
and 6 week postnatal brains, c-ski gene transcripts are also detected
in the hippocampus and in the granule cell layer of the cerebellum. T
he allantois and placenta exhibit high levels of c-ski mRNAs. Neonatal
lung tissue increases c-ski gene expression approximately two-fold co
mpared to prenatal levels. These results suggest that ski plays a role
in both the proliferation and differentiation of specific cell popula
tions of the central and peripheral nervous systems and of other tissu
es. (C) 1994 Wiley-Liss, Inc.