Liu Ye, Festing Maria H, Hester Mark, Thompson John C, Weinstein Michael
Molecular, Cellular, and Developmental Biology Program, The Ohio State University, Columbus, OH 43210, USA.
Genesis. 2004 Oct;40(2):118-123. doi: 10.1002/gene.20072.
Smad2 is an intracellular mediator of the transforming growth factor beta signaling (TGFbeta) pathway. It has been previously shown that, in the mouse, ablation of functional Smad2 results in embryonic lethality due to gastrulation defects. To circumvent the early lethality and study the spatially and temporally specific functions of Smad2, we utilized the Cre-loxP system to generate a Smad2 conditional allele. Here we show that a conditional allele, Smad2(flox), was generated. In this allele, exons 9 and 10 are flanked by loxP sites and the gene is functionally wildtype. Cre-mediated recombination results in a deletion allele which phenocopies our previously reported Smad2(DeltaC) null mutation. To generate this conditional allele, we first made a targeted mutation which introduced a floxed neo cassette into intron 10. This allele (Smad2(3loxP)) functions hypomorphically when placed opposite a null allele, and unlike the other published Smad2 hypomorphic allele, can be maintained in the homozygous state.
Smad2是转化生长因子β信号通路(TGFβ)的细胞内介质。先前已表明,在小鼠中,功能性Smad2的缺失会由于原肠胚形成缺陷导致胚胎致死。为了规避早期致死性并研究Smad2在空间和时间上的特定功能,我们利用Cre-loxP系统生成了一个Smad2条件等位基因。在此我们表明生成了一个条件等位基因Smad2(flox)。在这个等位基因中,外显子9和10两侧是loxP位点,该基因在功能上是野生型。Cre介导的重组产生一个缺失等位基因,其表型模拟了我们先前报道的Smad2(DeltaC)无效突变。为了生成这个条件等位基因,我们首先进行了一个靶向突变,将一个floxed新霉素盒引入内含子10。当与一个无效等位基因相对放置时,这个等位基因(Smad2(3loxP))功能减弱,并且与其他已发表的Smad2功能减弱等位基因不同,它可以保持纯合状态。