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CPEB mediated ZO-1 mRNA Localization is Required for Epithelial Tight Junction Assembly and Cell Polarity

机译:CPEB介导的ZO-1 mRNA定位对于上皮紧密连接组装和细胞极性是必需的

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摘要

CPEB is a translational regulatory sequence-specific RNA binding protein that controls germ cell development. Here we show that CPEB heterozygous female mice are fertile but contain disorganized mammary epithelial cells in which ZO-1 and claudin-3, apical tight junction proteins, are mis-localized. CPEB depletion from mammary epithelial cells disrupts ZO-1 apical localization and tight junction distribution; conversely, ectopic expression of CPEB enhances ZO-1 localization. CPEB and ZO-1 mRNA are co-localized apically and ZO-1 3’UTR binding sites for CPEB are necessary for RNA localization. In a 3-dimensional culture system that models lumen-containing mammary ducts, depletion of CPEB or ZO-1 impairs central cavity formation, indicating a loss of cell polarity. Cavity formation in ZO-1 depleted cells is rescued when they are transduced with ZO-1 mRNA containing, but not lacking, CPEB binding sites. Our data demonstrates that CPEB-mediated ZO-1 mRNA localization is essential for tight junction assembly and mammary epithelial cell polarity.
机译:CPEB是控制生殖细胞发育的翻译调控序列特异性RNA结合蛋白。在这里,我们显示CPEB杂合雌性小鼠可育,但包含杂乱的乳腺上皮细胞,其中ZO-1和claudin-3(顶端紧密连接蛋白)被错误定位。乳腺上皮细胞的CPEB耗竭破坏了ZO-1顶端的定位和紧密的连接分布;相反,CPEB的异位表达增强了ZO-1的定位。 CPEB和ZO-1 mRNA在根尖共定位,而CPEB的ZO-1 3’UTR结合位点对于RNA定位是必需的。在一个三维模型的培养系统中,模拟包含内腔的乳腺导管,CPEB或ZO-1的耗竭会削弱中央腔的形成,表明细胞极性的丧失。当用含有但不缺乏CPEB结合位点的ZO-1 mRNA进行转导时,可以挽救ZO-1耗尽细胞中的空洞形成。我们的数据表明,CPEB介导的ZO-1 mRNA定位对于紧密连接装配和乳腺上皮细胞极性至关重要。

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