Characterization of transgenic mice expressing cancer-associated variants of human NOTCH1

被引:5
|
作者
Berquam-Vrieze, Katherine E. [1 ]
Swing, Deborah A. [2 ]
Tessarollo, Lino [2 ]
Dupuy, Adam J. [1 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Anat & Cell Biol, Iowa City, IA 52242 USA
[2] NCI, Mouse Canc Genet Program, Frederick, MD 21701 USA
关键词
mouse models of cancer; BAC recombineering; BAC transgenesis; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACTIVATED NOTCH1; PROGRESSION; MUTATIONS; APOPTOSIS; BINDING; GENES; CELLS; CD4;
D O I
10.1002/dvg.20798
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Notch1 receptor plays a critical role in cell fate decisions during development. Activation of Notch signaling has been implicated in several types of cancer, particularly T-cell acute lymphoblastic leukemia (T-ALL). Consequently, several transgenic mouse strains have been made to study the role of Notch1 in T-ALL. However, the existing Notch1 transgenic lines mimic a translocation event found in only similar to 1% of T-ALL cases. Here we describe three novel NOTCH1 transgenic mouse strains that have Cre-inducible expression of the entire human NOTCH1 locus, each possessing a common mutation found in T-ALL. Unlike existing Notch1 transgenic strains, these NOTCH1 transgenic strains express full-length receptors from anendogenous human promoter that should be susceptible to a number of Notch antagonists that have recently been developed. These strains will allow researchers to modulate Notch signaling to study bothnormal development and cancer biology. genesis 50:112118, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:112 / 118
页数:7
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