This work provides insight the function of Src proto-oncogene in neurogenes
is by immunohistochemically investigating the distribution and time course
of development of 8 src-related protein-tyrosine kinases (c-Src, Fyn, Yes,
Lyn, Lck, Hck, Fgr, Blk) in vivo in the developing nervous system of a mous
e. Experimental results indicate that all members of Src family are express
ed early in dividing cells in the neural plate by embryonic day 8 and, then
, maintained in the central and peripheral nervous system until late prenat
al stages. The immunoreactivity is widely distributed not only in the brain
and spinal cord, but also in neural crest-derived structures, including sp
inal and sympathetic ganglia. Src-positive structures found in the fetal br
ain are primarily located in the forebrain and diencephalon. In addition, h
igh levels of immunoreactivity can be observed in special sensory organs su
ch as the retina and otic vesicle. Although various members closely resembl
e each other in terms of the overall pattern of immunoreactivity, implying
an overlapping functional aspects of different members of the family, a sli
ght difference arises in the time course of expression and staining intensi
ty. Moreover, the early appearance, high levels and wide distribution of in
dividual members of the Src family in the mouse's nervous system suggest th
at these gene products profoundly influence neuronal differentiation and ma
turation.