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果蝇致死(2)巨幼虫肿瘤抑制蛋白是细胞骨架的一个组成部分。

The Drosophila lethal(2)giant larvae tumor suppressor protein is a component of the cytoskeleton.

作者信息

Strand D, Raska I, Mechler B M

机构信息

Department of Developmental Genetics, Deutsches Krebsforschungszentrum, Germany.

出版信息

J Cell Biol. 1994 Dec;127(5):1345-60. doi: 10.1083/jcb.127.5.1345.

Abstract

Tumor suppressor genes act as recessive determinants of cancer. In Drosophila these genes play a role in normal development and are essential for regulating cell growth and differentiation. Mutations in the gene, lethal(2)giant larvae, l(2)gl, besides causing malignant tumors in the brain and imaginal discs, generate developmental defects in a number of other tissues. Much of the uncertainty regarding the function of the l(2)gl gene product, p127, results from a lack of knowledge as to the precise location of this protein in the cell. We have investigated the cellular and subcellular localization of p127, using confocal and electron microscopy as well as biochemical and cell fractionation procedures. Our analyses indicate that p127 is located entirely within the cell in both the cytoplasm and bound to the inner face of lateral cell membranes in regions of cell junctions. On the membrane, p127 can form large aggregates which are resistant to solubilization by nonionic detergents, indicating that p127 is participating in a cytoskeletal matrix. These findings suggest that the changes in cell shape and the loss of apical-basal polarity observed in tumorous tissues are a direct result of alterations in the cytoskeleton organization caused by l(2)gl inactivation and also suggest that p127 is involved in a cytoskeletal-based intercellular communication system directing cell differentiation.

摘要

肿瘤抑制基因作为癌症的隐性决定因素。在果蝇中,这些基因在正常发育中发挥作用,对调节细胞生长和分化至关重要。致死(2)巨型幼虫基因l(2)gl发生突变,除了会在大脑和成虫盘引发恶性肿瘤外,还会在许多其他组织中产生发育缺陷。关于l(2)gl基因产物p127功能的许多不确定性,源于对该蛋白在细胞中精确位置缺乏了解。我们利用共聚焦显微镜和电子显微镜以及生化和细胞分级分离程序,研究了p127在细胞和亚细胞水平的定位。我们的分析表明,p127完全位于细胞内,既存在于细胞质中,又在细胞连接区域与外侧细胞膜的内表面结合。在细胞膜上,p127可形成对非离子去污剂溶解有抗性的大聚集体,这表明p127参与了细胞骨架基质。这些发现表明,在肿瘤组织中观察到的细胞形状变化和顶-基极性丧失,是由l(2)gl失活导致的细胞骨架组织改变的直接结果,也表明p127参与了指导细胞分化的基于细胞骨架的细胞间通讯系统。

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