The rat insulin promoter (RIP) has been used to drive the expression of Cre
recombinase (Cre) specifically in beta cells. Transient transfection was p
erformed in the mouse insulinoma cell line, NIT-I, and control cell lines.
RT-PCR was performed using total RNA from pancreas and other tissues of RIP
-Cre transgenic mice. In addition, the efficiency and specificity of RIP we
re further analyzed by cross breeding the RIP-Cre transgenic mice with repo
rter mice bearing a beta-actin-loxP-CAT-loxP-lacZ transgene. In these mice,
lacZ is expressed only after excision of the floxed-CAT gene by Cre-mediat
ed recombination. Here, we present the data for beta cell-specific expressi
on of lacZ in bigenic mice, as proof of concept in a mouse model for target
ing beta cell-specific gene(s). The RIP-Cre transgenic mice will be used as
a potential tool for targeting the excision of beta cell-specific gene(s)
to study their role in islet cell physiology. (C) 1998 Academic Press.