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用于在内胚层、脊索和底板中从Foxa2基因座诱导表达cre重组酶的系统。

System for inducible expression of cre-recombinase from the Foxa2 locus in endoderm, notochord, and floor plate.

作者信息

Frank Deborah U, Elliott Sarah A, Park Eon Joo, Hammond Jennetta, Saijoh Yukio, Moon Anne M

机构信息

Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA.

出版信息

Dev Dyn. 2007 Apr;236(4):1085-92. doi: 10.1002/dvdy.21093.

Abstract

We targeted the reverse tetracycline controlled transactivator (rtTA) to the Foxa2 locus (Foxa2(ITA)) to generate a system for regulating Cre-recombinase activity within Foxa2 expression domains, including the endoderm, notochord, and floor plate of early mouse embryos. The use of an internal ribosomal entry site to obtain rtTA expression preserves Foxa2 function of the targeted allele. Cre activity with this system reflects the level of endogenous Foxa2 activity and is also tightly controlled by doxycycline. The location of Cre activity within the broader Foxa2 expression domain can be restricted by altering the timing of doxycycline administration. Isolated floor plate expression can be obtained in this manner. This system will provide a useful tool for manipulating gene expression in endoderm, notochord, and floor plate, all of which are tissues with important structural and patterning functions during embryogenesis.

摘要

我们将反向四环素调控反式激活因子(rtTA)靶向定位于Foxa2基因座(Foxa2(ITA)),以构建一个在Foxa2表达域(包括早期小鼠胚胎的内胚层、脊索和底板)内调节Cre重组酶活性的系统。利用内部核糖体进入位点来获得rtTA表达可保留靶向等位基因的Foxa2功能。该系统的Cre活性反映了内源性Foxa2活性水平,并且也受到强力霉素的严格调控。通过改变强力霉素给药时间,可以将Cre活性在更广泛的Foxa2表达域内的位置进行限制。以这种方式可以获得孤立的底板表达。该系统将为在内胚层、脊索和底板中操纵基因表达提供一个有用的工具,所有这些组织在胚胎发育过程中都具有重要的结构和模式形成功能。

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