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首页> 外文期刊>Molecular biology of the cell >Mammalian homolog of Drosophila tumor suppressor lethal (2) giant larvae interacts with basolateral exocytic machinery in Madin-Darby canine kidney cells
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Mammalian homolog of Drosophila tumor suppressor lethal (2) giant larvae interacts with basolateral exocytic machinery in Madin-Darby canine kidney cells

机译:果蝇抑癌药致死性(2)的巨型幼虫的哺乳动物同源物与Madin-Darby犬肾细胞的基底外侧外生机制相互作用

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摘要

The Drosophila tumor suppressor protein lethal (2) giant larvae [l(2)gl] is involved in the establishment of epithelial cell polarity during development. Recently, a yeast homolog of the protein has been shown to interact with components of the post-Golgi exocytic machinery and to regulate a late step in protein secretion. Herein, we characterize a mammalian homolog of l(2)gl, called Mlgl, in the epithelial cell line Madin-Darby canine kidney (MDCK). Consistent with a role in cell polarity, Mlgl redistributes from a cytoplasmic localization to the lateral membrane after contact-naive MDCK cells make cell-cell contacts and establish a polarized phenotype. Phosphorylation within a highly conserved region of Mlgl is required to restrict the protein to the lateral domain, because a recombinant phospho-mutant is distributed in a nonpolar manner. Membrane-bound Mlgl from MDCK cell lysates was coimmunoprecipitated with syntaxin 4, a component of the exocytic machinery at the basolateral membrane, but not with other plasma membrane soluble N-ethylmaleimide-sensitive factor attachment receptor (SNARE) proteins that are either absent from or not restricted to the basolateral membrane domain. These data suggest that Mlgl contributes to apico-basolateral polarity by regulating basolateral exocytosis. [References: 35]
机译:果蝇肿瘤抑制蛋白致死性(2)巨型幼虫[l(2)gl]参与发育过程中上皮细胞极性的建立。最近,该蛋白质的酵母同源物已经显示出与高尔基体后胞外机制的成分相互作用,并调节蛋白质分泌的后期步骤。本文中,我们在上皮细胞系Madin-Darby犬肾(MDCK)中表征了称为Mlgl的l(2)gl的哺乳动物同源物。与细胞极性作用一致,未经接触的MDCK细胞与细胞接触并建立极化表型后,Mlg1从细胞质定位重新分布到侧膜。由于重组磷酸突变体以非极性方式分布,因此需要在Mlgl高度保守的区域内进行磷酸化以将蛋白质限制在侧结构域。将来自MDCK细胞裂解物的膜结合Mlg1与语法蛋白4共沉淀,该蛋白是基底外侧膜上胞外机制的组成部分,而不与其他质膜可溶性N-乙基马来酰亚胺敏感因子附着受体(SNARE)蛋白不存在或不存在。不限于基底外侧膜结构域。这些数据表明,Mlg1通过调节基底外侧胞吐作用而促进了apico-基底外侧极性。 [参考:35]

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