共 102 条
Rho regulation: DLC proteins in space and time
被引:59
作者:
Braun, Anja C.
[1
]
Olayioye, Monilola A.
[1
]
机构:
[1] Univ Stuttgart, Inst Cell Biol & Immunol, D-70569 Stuttgart, Germany
关键词:
Deleted in liver cancer 1-3 (DLC1/StarD12;
DLC2/StarD13;
DLC3/StarD8);
Rho signaling;
GTPase activating protein (GAP);
Subcellular localization;
Tumor suppression;
GTPASE-ACTIVATING PROTEIN;
TUMOR-SUPPRESSOR PROTEIN;
CONTROLS CELL-MIGRATION;
CANCER;
DLC1;
ADHERENS JUNCTIONS;
FOCAL ADHESIONS;
CROSSVEINLESS-C;
PLC-DELTA(1)-BINDING PROTEIN;
HEPATOCELLULAR-CARCINOMA;
MORPHOLOGICAL-CHANGES;
D O I:
10.1016/j.cellsig.2015.04.003
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Rho GTPases function as molecular switches that connect changes of the external environment to intracellular signaling pathways. They are active at various subcellular sites and require fast and tight regulation to fulfill their role as transducers of extracellular stimuli. New imaging technologies visualizing the active states of Rho proteins in living cells elucidated the necessity of precise spatiotemporal activation of the GTPases. The local regulation of Rho proteins is coordinated by the interaction with different guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPS) that turn on and off GTPase signaling to downstream effectors. GEFs and GAPs thus serve as critical signaling nodes that specify the amplitude and duration of a particular Rho signaling pathway. Despite their importance in Rho regulation, the molecular aspects underlying the spatiotemporal control of the regulators themselves are still largely elusive. In this review we will focus on the Deleted in Liver Cancer (DLC) family of RhoGAP proteins and summarize the evidence gathered over the past years revealing their different subcellular localizations that might account for isoform-specific functions. We will also highlight the importance of their tightly controlled expression in the context of neoplastic transformation. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1643 / 1651
页数:9
相关论文