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鉴定一种参与膜皱褶形成的新型Rac1相互作用蛋白。

Identification of a novel Rac1-interacting protein involved in membrane ruffling.

作者信息

Van Aelst L, Joneson T, Bar-Sagi D

机构信息

Cold Spring Harbor Laboratory, PO Box 100, Cold Spring Harbor, NY 11724, USA.

出版信息

EMBO J. 1996 Aug 1;15(15):3778-86.

Abstract

The Rac GTP binding proteins are implicated in actin cytoskeleton-membrane interaction in mammalian cells. In fibroblast cells, Rac has been shown to mediate growth factor-induced polymerization of actin to form membrane ruffles and lamellipodia. We report here the isolation of a noval Rac1-interacting protein, POR1. POR1 binds directly to Rac1, and the interaction of POR1 with Rac1 is GTP dependent. A mutation in the Rac1 effector binding loop shown to abolish membrane ruffling also abolishes interaction with POR1. Truncated versions of POR1 inhibit the induction of membrane ruffling by an activated mutant of Rac1, V12Rac1, in quiescent rat embryonic fibroblast REF52 cells. Furthermore, POR1 synergizes with an activated mutant of Ras, V12Ras, in the induction of membrane ruffling. These results suggest a potential role for POR1 in Rac1-mediated signaling pathways.

摘要

Rac GTP结合蛋白与哺乳动物细胞中的肌动蛋白细胞骨架-膜相互作用有关。在成纤维细胞中,Rac已被证明能介导生长因子诱导的肌动蛋白聚合,形成膜皱褶和片状伪足。我们在此报告一种新型Rac1相互作用蛋白POR1的分离。POR1直接与Rac1结合,且POR1与Rac1的相互作用依赖于GTP。Rac1效应器结合环中的一个突变显示可消除膜皱褶,该突变也消除了与POR1的相互作用。POR1的截短版本可抑制静息大鼠胚胎成纤维细胞REF52中Rac1激活突变体V12Rac1诱导的膜皱褶。此外,POR1与Ras激活突变体V12Ras协同诱导膜皱褶。这些结果表明POR1在Rac1介导的信号通路中可能发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e92/452058/c99e4ba0d34c/emboj00015-0016-a.jpg

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