The cerebellar cortex and its sole output, the Purkinje cell, have been imp
licated in motor coordination, learning and cognitive functions. Therefore,
the ability to generate Purkinje cell-specific mutations in physiologicall
y relevant genes is of particular neurobiological interest. A suitable appr
oach is the Cre/loxP strategy that allows temporally and spatially controll
ed gene inactivation. Here, we present the characterization of transgenic m
ouse strains expressing Cre recombinase controlled by the L7/pcp-2 gene. En
dogenous L7/pcp-2 protein is expressed exclusively in Purkinje cells and re
tinal bipolar neurones. Recombination was detected by beta -galactosidase h
istochemistry in tissues from crosses of the L7/pcp-2:Cre transgenic lines
with two different indicator strains, GtROSA26 and ACZL. Purkinje cells in
all folia of the cerebellum displayed intense beta -galactosidase staining,
whereas only few blue cells were observed in the retina and other parts of
the CNS, Thus, these transgenic lines are potentially of great importance
for genetic manipulations in cerebellar Purkinje cells. (C) 2000 Wiley-Liss
, Inc.