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两种PDZ结构域蛋白Canoe和ZO-1之间的直接结合及其在果蝇形态发生中对Jun N端激酶途径的调控作用。

Direct binding between two PDZ domain proteins Canoe and ZO-1 and their roles in regulation of the jun N-terminal kinase pathway in Drosophila morphogenesis.

作者信息

Takahashi K, Matsuo T, Katsube T, Ueda R, Yamamoto D

机构信息

Mitsubishi Kasei Institute of Life Sciences, Machida, Tokyo 194-8511, Japan.

出版信息

Mech Dev. 1998 Nov;78(1-2):97-111. doi: 10.1016/s0925-4773(98)00151-8.

Abstract

During Drosophila embryogenesis, the ventral epidermis dorsally expands and the left and right epithelial sheets meet and fuse along the dorsal midline. For this dorsal closure to occur, two PDZ domain proteins, Cno and ZO-1, are required. The dorsal epidermis remains open when the expression of ZO-1 and Cno are reduced simultaneously by hypomorphic mutations in the relevant loci. ZO-1 and Cno colocalize at adherens junctions in embryonic epithelia, and form a protein complex upon binding to each other. Genetic analysis showed that Cno is involved in the Jun N-terminal kinase (JNK) pathway for dorsal closure, as a modulator acting upstream of, or in parallel with, the small GTPase Drac1. The ZO-1-Cno complex may be involved in dynamic changes in cytoskeletal organization and cell adhesion during morphogenetic events associated with dorsal closure in the Drosophila embryo.

摘要

在果蝇胚胎发育过程中,腹侧表皮向背侧扩展,左右上皮层在背中线处相遇并融合。为了实现这种背侧闭合,需要两种PDZ结构域蛋白,即Cno和ZO-1。当相关基因座的亚效突变同时降低ZO-1和Cno的表达时,背侧表皮会保持开放状态。ZO-1和Cno在胚胎上皮细胞的黏着连接处共定位,并在相互结合时形成蛋白质复合物。遗传分析表明,Cno作为一种调节剂,在小GTP酶Drac1的上游或与其平行发挥作用,参与背侧闭合的Jun N端激酶(JNK)信号通路。ZO-1-Cno复合物可能参与果蝇胚胎背侧闭合相关形态发生事件中细胞骨架组织和细胞黏附的动态变化。

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