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A Cre-inducible fluorescent reporter for observing apical membrane dynamics

机译:Cre诱导型荧光报告基因用于观察根尖膜动力学

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摘要

The ability to image living tissues with fluorescent proteins has revolutionized the fields of cell and developmental biology. Fusions between fluorescent proteins and various polypeptides are allowing scientists to image tissues with sub-cellular resolution. Here, we describe the generation and activity of a genetically engineered mouse line expressing a fusion between the green fluorescent protein (GFP) and the apically localized protein Crumbs3 (Crb3). This reporter drives Cre inducible expression of Crb3-GFP under control of the EF1a regulatory domains. The fusion protein is broadly expressed in embryonic and adult tissues and shows apical restriction in the majority of epithelial cell types. It displays a variably penetrant gain of function activity in the neural tube. However, in several cell types, over-expression of Crb3 does not appear to have any affect on normal development or maintenance. Detailed analysis of kidneys expressing this reporter indicates normal morphology and function highlighting the utility for live imaging. Thus, the EF1aCrb3-GFP mouse line will be of broad use for studying membrane and/or tissue dynamics in living tissues.
机译:用荧光蛋白成像活组织的能力彻底改变了细胞和发育生物学领域。荧光蛋白和各种多肽之间的融合使科学家能够以亚细胞分辨率对组织成像。在这里,我们描述了表达绿色荧光蛋白(GFP)与根尖蛋白Crumbs3(Crb3)之间融合的基因工程小鼠品系的产生和活性。该报道分子在EF1a调节域的控制下驱动Cre诱导的Crb3-GFP表达。融合蛋白在胚胎和成年组织中广泛表达,并且在大多数上皮细胞类型中显示出顶端限制。它显示了神经管中功能活动的不同渗透性增加。但是,在几种细胞类型中,Crb3的过度表达似乎对正常发育或维持没有任何影响。对表达该报道分子的肾脏进行的详细分析表明其正常的形态和功能突显了实时成像的实用性。因此,EF1a Crb3-GFP 小鼠系将广泛用于研究活组织中的膜和/或组织动力学。

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