Second-generation Notch1 activity-trap mouse line (N1IP::CreHI) provides a more comprehensive map of cells experiencing Notch1 activity

被引:15
作者
Liu, Zhenyi [1 ,2 ]
Brunskill, Eric [3 ]
Boyle, Scott [2 ]
Chen, Shuang [2 ,3 ]
Turkoz, Mustafa [2 ,3 ]
Guo, Yuxuan [2 ,4 ]
Grant, Rachel [2 ]
Kopan, Raphael [2 ,3 ]
机构
[1] SAGE Labs, St Louis, MO 63146 USA
[2] Washington Univ, Dept Dev Biol, St Louis, MO 63110 USA
[3] Childrens Hosp, Med Ctr, Div Dev Biol, Cincinnati, OH 45229 USA
[4] Carnegie Inst Sci, Dept Embryol, Baltimore, MD 21218 USA
来源
DEVELOPMENT | 2015年 / 142卷 / 06期
基金
美国国家卫生研究院;
关键词
Activity; Cre; Neuron; Notch1; Kidney; SITE-SPECIFIC RECOMBINATION; STEM-CELLS; SERTOLI-CELLS; MAMMALIAN NEUROGENESIS; EMBRYONIC LETHALITY; FOLLICLE FORMATION; SIGNALING PATHWAY; DROSOPHILA OVARY; NICHE FORMATION; GERM-LINE;
D O I
10.1242/dev.119529
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
We have previously described the creation and analysis of a Notch1 activity-trap mouse line, Notch1 intramembrane proteolysis-Cre6MT or N1IP::Cre(LO), that marked cells experiencing relatively high levels of Notch1 activation. Here, we report and characterize a second line with improved sensitivity (N1IP::Cre(HI)) to mark cells experiencing lower levels of Notch1 activation. This improvement was achieved by increasing transcript stability and by restoring the native carboxy terminus of Cre, resulting in a five- to tenfold increase in Cre activity. The magnitude of this effect probably impacts Cre activity in strains with carboxy-terminal Ert2 fusion. These two trap lines and the related line N1IP::Cre(ERT2) form a complementary mapping tool kit to identify changes in Notch1 activation patterns in vivo as the consequence of genetic or pharmaceutical intervention, and illustrate the variation in Notch1 signal strength from one tissue to the next and across developmental time.
引用
收藏
页码:1193 / 1202
页数:10
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