Z/AP, a double reporter for Cre-mediated recombination

被引:432
作者
Lobe, CG
Koop, KE
Kreppner, W
Lomeli, H
Gertsenstein, M
Nagy, A
机构
[1] Sunnybrook Hlth Sci Ctr, Canc Res Div, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[3] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON, Canada
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[5] McMaster Univ, Dept Med Sci, Hamilton, ON L8S 3K5, Canada
基金
英国医学研究理事会;
关键词
Cre; loxP; transgenic mice; conditional genome alteration; lacZ; alkaline phosphatase; reporter;
D O I
10.1006/dbio.1999.9209
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Cre/loxP site-specific recombination system combined with embryonic stem cell-mediated technologies has greatly expanded our capability to address normal and disease development in mammals using genetic approaches. The success of this emerging technology hinges on the production of Cre-expressing transgenic lines that provide cell type-, tissue-, or developmental stage-specific recombination between loxP sites placed in the genome. Here we describe and characterize the production of a double-reporter mouse line that provides a convenient and reliable readout of Cre recombinase activity. Throughout all embryonic and adult stages, the transgenic animal expresses the lacZ reporter gene before Cre-mediated excision occurs. Cre excision, however, removes the lacZ gene, allowing expression of the second reporter, the human alkaline phosphatase gene. This double-reporter transgenic line is able to indicate the occurrence of Cre excision in an extremely widespread manner from early embryonic to adult lineages. It will be a valuable reagent for the increasing number of investigators taking advantage of the powerful tools provided by the Cre/loxP site-specific recombinase system. (C) 1999 Academic Press.
引用
收藏
页码:281 / 292
页数:12
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