Ras acylation, compartmentalization and signaling nanoclusters (Review)

被引:95
作者
Henis, Yoav I. [3 ]
Hancock, John F. [2 ]
Prior, Ian A. [1 ]
机构
[1] Univ Liverpool, Sch Biomed Sci, Physiol Lab, Liverpool L69 3BX, Merseyside, England
[2] Univ Texas Hlth Sci Ctr, Dept Integrat Biol & Pharmacol, Houston, TX USA
[3] Tel Aviv Univ, Dept Neurobiol, George S Wise Fac Life Sci, IL-69978 Tel Aviv, Israel
关键词
Palmitoylation; GTPase; isoforms; plasma membrane; nanoclusters; PLASMA-MEMBRANE LOCALIZATION; SINGLE-MOLECULE TRACKING; RAFT-ASSOCIATED PROTEINS; ORDERED LIPID DOMAINS; GPI-ANCHORED PROTEINS; ONCOGENIC H-RAS; K-RAS; CELL-SURFACE; N-RAS; SACCHAROMYCES-CEREVISIAE;
D O I
10.1080/09687680802649582
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ras proteins have become paradigms for isoform- and compartment-specific signaling. Recent work has shown that Ras isoforms are differentially distributed within cell surface signaling nanoclusters and on endomembranous compartments. The critical feature regulating Ras protein localization and isoform-specific functions is the C-terminal hypervariable region (HVR). In this review we discuss the differential post-translational modifications and reversible targeting functions of Ras isoform HVR motifs. We describe how compartmentalized Ras signaling has specific functional consequences and how cell surface signaling nanoclusters generate precise signaling outputs.
引用
收藏
页码:80 / 92
页数:13
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