Germ line activation of the Tie2 and SMMHC promoters causes noncell-specific deletion of floxed alleles

被引:59
作者
de Lange, Willem J.
Halabi, Carmen M. [2 ]
Beyer, Andreas M. [2 ]
Sigmund, Curt D. [1 ,3 ,4 ]
机构
[1] Univ Iowa, Dept Internal Med, Roy J & Lucille Carver Coll Med, Med Educ & Biomed Res Facil 3181B, Iowa City, IA 52242 USA
[2] Univ Iowa, Grad Program Genet, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Mol Physiol & Biophys, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
[4] Univ Iowa, Ctr Funct Genom Hypertens, Roy J & Lucille Carver Coll Med, Iowa City, IA 52242 USA
关键词
Cre-loxP; knockout; conditional; vascular; endothelium; smooth muscle myosin heavy chain;
D O I
10.1152/physiolgenomics.90284.2008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
de Lange WJ, Halabi CM, Beyer AM, Sigmund CD. Germ line activation of the Tie2 and SMMHC promoters causes noncell-specific deletion of floxed alleles. Physiol Genomics 35: 1-4, 2008. First published July 8, 2008; doi: 10.1152/physiolgenomics.90284.2008.-Tissue-specific knockouts generated through Cre-loxP recombination have become an important tool to manipulate the mouse genome. Normally, two successive rounds of breeding are performed to generate mice carrying two floxed target-gene alleles and a transgene expressing Cre-recombinase tissue-specifically. We show herein that two promoters commonly used to generate endothelium-specific (Tie2) and smooth muscle-specific [smooth muscle myosin heavy chain (Smmhc)] knockout mice exhibit activity in the female and male germ lines, respectively. This can result in the inheritance of a null allele in the second generation that is not tissue specific. Careful experimental design is required therefore to ensure that tissue-specific knockouts are indeed tissue specific and that appropriate controls are used to compare strains.
引用
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页码:1 / 4
页数:4
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