The Cre/loxP recombination system allows the generation of tissue-specific
somatic mutations in mice. Additional temporal control of somatic mutagenes
is is highly desirable, as this would permit a more precise analysis of gen
e function in complex systems such as the central nervous system. Extending
our previous studies, we compared several ligand-regulated recombinases, i
n which the ligand-binding domain (LBD) of the progesterone receptor or the
estrogen receptor was fused to the Cre recombinase. A fusion protein betwe
en the Cre recombinase and a truncated LED of the progesterone receptor was
chosen to obtain inducible recombination in the brain. This fusion protein
can be activated by the synthetic steroid RU486, but not by the physiologi
cal hormone progesterone. Its expression was targeted to the brain using re
gulatory sequences of the calcium-calmodulin-dependent kinase II alpha or t
he Thy-1 gene. Application of RU486 to the mice induced Cre-mediated recomb
ination of a lacZ reporter transgene in the cortex and hippocampus, showing
that spatially and temporally controlled gene targeting can be mediated in
the brain. (C) 1999 Academic Press.