期刊
MOLECULAR AND CELLULAR BIOLOGY
卷 25, 期 11, 页码 4602-4614出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.25.11.4602-4614.2005
关键词
-
资金
- NCI NIH HHS [CA47391, R01 CA095559, R01 CA047391, CA95559] Funding Source: Medline
- NIDDK NIH HHS [P30 DK034928, P30-DK34928] Funding Source: Medline
The exchange factor Tiam1 regulates multiple cellular functions by activating the Rac GTPase. Active Rac has various effects in cells, including alteration of actin cytoskeleton and gene expression, via binding to and modulating the activity of diverse effector proteins. How individual Rac effectors are selected for activation and regulated in response to upstream signals is not well understood. We find that Tiam1 contributes to both of these processes by binding to IRSp53, an adaptor protein that is an effector for both Rac and Cdc42. Tiam1 directs IRSp53 to Rac signaling by enhancing IRSp53 binding to both active Rac and the WAVE2 scaffold. Moreover, Tiam1 promotes IRSp53 localization to Rac-induced lamellipodia rather than Cdc42-induced filopodia. Finally, IRSp53 depletion from cells prevents Tiam1-dependent lamellipodia induced by Tiam1 overexpression or platelet-derived growth factor stimulation. These findings indicate that Tiam1 not only activates Rac but also contributes to Rac signaling specificity through binding to IRSp53.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据