A genomic done encoding the Purkinje cell-specific L7 protein has been isolated and utilized to drive the expression of β-galactosidase in mice. Three independent transgenic lines, germ line transformed with an L7-β-galactosidase fusion gene, exhibit β-galactosidase expression in both cerebellar Purkinje cells and retinal bipolar neurons. This distribution is the same as that previously determined for the L7 protein by immunohistochemistry. The transgenic murine lines can be used to obtain populations of marked Purkinje and bipolar neurons. Similar L7 promoter constructs can be used to express other foreign genes specifically in these two classes of neurons.
|Number of pages||4|
|Publication status||Published - 1990|