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利用新型 sm22α-b 启动子对斑马鱼肠道平滑肌发育进行特征描述。

Characterization of zebrafish intestinal smooth muscle development using a novel sm22α-b promoter.

机构信息

Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

出版信息

Dev Dyn. 2010 Nov;239(11):2806-12. doi: 10.1002/dvdy.22420.

Abstract

Smooth muscle cells provide structural support for many tissues and control essential physiological processes, such as blood pressure and gastrointestinal motility. Relatively little is known about the early stages of intestinal smooth muscle development and its relationship to the development of the enteric nervous system, which regulates intestinal motility. Here, we report an evolutionarily conserved 523 base pair regulatory element within the promoter of the zebrafish sm22α-b (transgelin1) gene that directs transgene expression in smooth muscle cells of the intestine and other tissues. Comparative genomic analysis identified a conserved motif within this element consisting of two Serum Response Factor binding sites that is also present in the promoters of many mammalian smooth muscle genes. We established a stable line expressing GFP in smooth muscle cell and used this line to describe lineage relationships among cells within different intestinal smooth muscle layers and their co-development with the enteric nervous system (ENS).

摘要

平滑肌细胞为许多组织提供结构支持,并控制着血压和胃肠道蠕动等重要的生理过程。然而,人们对于肠道平滑肌的早期发育及其与调节肠道蠕动的肠神经系统发育之间的关系了解甚少。在这里,我们报道了一个在斑马鱼 sm22α-b(转谷氨酰胺酶 1)基因启动子内的保守的 523 个碱基对的调控元件,该元件可以指导转基因在肠道和其他组织的平滑肌细胞中的表达。比较基因组分析鉴定出该元件内的一个保守基序,该基序由两个血清反应因子结合位点组成,该基序也存在于许多哺乳动物平滑肌基因的启动子中。我们建立了一个在平滑肌细胞中表达 GFP 的稳定系,并利用该系描述了不同肠道平滑肌层内细胞之间的谱系关系及其与肠神经系统(ENS)的共同发育。

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