Regulating the regulator: post-translational modification of RAS

被引:412
作者
Ahearn, Ian M. [1 ]
Haigis, Kevin [2 ]
Bar-Sagi, Dafna [1 ]
Philips, Mark R. [1 ]
机构
[1] NYU, Sch Med, New York, NY 10016 USA
[2] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
关键词
ISOPRENYLCYSTEINE CARBOXYL METHYLTRANSFERASE; GUANINE-NUCLEOTIDE EXCHANGE; BLADDER-CARCINOMA ONCOGENE; P21(RAS) S-NITROSYLATION; H-RAS; K-RAS; PLASMA-MEMBRANE; N-RAS; SIGNAL-TRANSDUCTION; LIPID RAFTS;
D O I
10.1038/nrm3255
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RAS proteins are monomeric GTPases that act as binary molecular switches to regulate a wide range of cellular processes. The exchange of GTP for GDP on RAS is regulated by guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs), which regulate the activation state of RAS without covalently modifying it. By contrast, post-translational modifications (PTMs) of RAS proteins direct them to various cellular membranes and, in some cases, modulate GTP-GDP exchange. Important RAS PTMs include the constitutive and irreversible remodelling of its carboxy-terminal CAAX motif by farnesylation, proteolysis and methylation, reversible palmitoylation, and conditional modifications, including phosphorylation, peptidyl-prolyl isomerisation, monoubiquitylation, diubiquitylation, nitrosylation, ADP ribosylation and glucosylation.
引用
收藏
页码:39 / 51
页数:13
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