Highly efficient transgene-independent recombination directed by a maternally derived Sox2Cre transgene

被引:30
作者
Vincent, SD [1 ]
Robertson, EJ [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 01238 USA
关键词
mouse; Cre recombination; gene deletion; female;
D O I
10.1002/gene.10226
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 is a powerful tool that allows gene inactivation in a tissue- and time-specific manner. Several reports have shown that the Sox2Cre transgenic strain provides a very efficient means to delete gene function from the early epiblast (Hayashi et al.: Gene Expr Patterns 2:9397, 2002; Vincent et al.: Genes Dev 17:1646-1662, 2003). Routinely, male studs carrying one null allele of the gene of interest and the Cre transgene are crossed to females homozygous for the conditional allele. Normally, excision is observed only in the progeny inheriting both the Cre transgene and the conditional allele. Here we report that when the Sox2Cre transgene is inherited maternally, excision occurs in all offspring irrespective of whether they carry the Cre transgene. Thus, Sox2Cre females provide a generally useful tool for rapid and efficient removal of loxP flanked sequences in vivo. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:54 / 56
页数:3
相关论文
共 12 条
[1]  
[Anonymous], 1994, MANIPULATING MOUSE E
[2]  
[Anonymous], 1983, COLD SPRING HARBOR L
[3]  
Hayashi Shigemi, 2002, Gene Expression Patterns, V2, P93, DOI 10.1016/S0925-4773(02)00292-7
[4]  
Nagy A, 2000, GENESIS, V26, P99, DOI 10.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO
[5]  
2-B
[6]   Protamine-Cre recombinase transgenes efficiently recombine target sequences in the male germ line of mice, but not in embryonic stem cells [J].
O'Gorman, S ;
Dagenais, NA ;
Qian, M ;
Marchuk, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14602-14607
[7]   A transgenic mouse line that retains Cre recombinase activity in mature oocytes irrespective of the cre transgene transmission [J].
Sakai, K ;
Miyazaki, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 237 (02) :318-324
[8]  
Vidal F, 1998, MOL REPROD DEV, V51, P274, DOI 10.1002/(SICI)1098-2795(199811)51:3&lt
[9]  
274::AID-MRD6&gt
[10]  
3.0.CO