Ohyama Takahiro
Division of Cell Biology and Genetics, House Ear Institute, 2100 West Third Street, Los Angeles, CA 90057, USA.
Brain Res. 2009 Jun 24;1277:84-9. doi: 10.1016/j.brainres.2009.02.036. Epub 2009 Mar 2.
One of the biggest drawbacks of conventional mouse knockout techniques in the study of the inner ear is that loss of a gene of interest may cause embryonic lethality before the inner ear develops. Thus, there is a need for an inner ear-specific gene manipulation system for loss- and gain-of-function analysis in the mouse inner ear. We generated a Pax2-Cre BAC transgenic line in which Cre recombinase expression recapitulates Pax2 expression in the presumptive otic ectoderm. Here, we present a brief summary of a recent model of inner ear induction suggested by the results of inner ear-specific gene modification using Pax2-Cre mice.
在内耳研究中,传统小鼠基因敲除技术的最大缺点之一是,感兴趣基因的缺失可能会在内耳发育之前导致胚胎致死。因此,需要一种内耳特异性基因操作体系,用于小鼠内耳功能缺失和功能获得分析。我们构建了一个Pax2-Cre BAC转基因品系,其中Cre重组酶的表达重现了Pax2在假定耳外胚层中的表达。在此,我们简要总结了利用Pax2-Cre小鼠进行内耳特异性基因修饰的结果所提示的一种最新内耳诱导模型。