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用于在发育中的心脏、腭和肢体中对基因进行组织特异性操纵的Shox2-Cre等位基因的产生。

Generation of Shox2-Cre allele for tissue specific manipulation of genes in the developing heart, palate, and limb.

作者信息

Sun Cheng, Zhang Tao, Liu Chao, Gu Shuping, Chen YiPing

机构信息

Department of Cell and Molecular Biology, Tulane University, New Orleans, LA 70118, USA.

出版信息

Genesis. 2013 Jul;51(7):515-22. doi: 10.1002/dvg.22397. Epub 2013 May 22.

Abstract

Shox2 is expressed in several developing organs in a tissue specific manner in both mice and humans, including the heart, palate, limb, and nervous system. To better understand the spatial and temporal expression patterns of Shox2 and to systematically dissect the genetic cascade regulated by Shox2, we created Shox2-LacZ and Shox2-Cre knock-in mouse lines. We show that the Shox2-LacZ allele expresses beta-galactosidase reporter gene in a fashion that recapitulates the endogenous Shox2 expression pattern in developing organs, including the sinoatrial node (SAN), the anterior portion of the palate, and the proximal region of the limb bud. Conditional deletion of Shox2 in mice carrying the Shox2-Cre allele yielded SAN phenotypes that resemble conventional Shox2 knockout mice. Our results indicate that the Shox2-Cre allele offer a useful tool for tissue specific manipulation of genes in a number of developing organs, particularly in the developing SAN.

摘要

在小鼠和人类中,Shox2在多个发育器官中以组织特异性方式表达,包括心脏、腭、肢体和神经系统。为了更好地理解Shox2的时空表达模式,并系统地剖析由Shox2调控的基因级联反应,我们创建了Shox2-LacZ和Shox2-Cre基因敲入小鼠品系。我们发现,Shox2-LacZ等位基因以一种重现发育器官(包括窦房结(SAN)、腭前部和肢芽近端区域)中内源性Shox2表达模式的方式表达β-半乳糖苷酶报告基因。在携带Shox2-Cre等位基因的小鼠中对Shox2进行条件性缺失产生了类似于传统Shox2基因敲除小鼠的SAN表型。我们的结果表明,Shox2-Cre等位基因为在多个发育器官,特别是在发育中的SAN中进行组织特异性基因操作提供了一个有用的工具。

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