Plasma membrane nanoswitches generate high-fidelity Ras signal transduction

被引:306
作者
Tian, Tianhai
Harding, Angus
Inder, Kerry
Plowman, Sarah
Parton, Robert G.
Hancock, John F. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Ctr Microscopy & Microanal, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1038/ncb1615
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ras proteins occupy dynamic plasma membrane nanodomains called nanoclusters. The significance of this spatial organization is unknown. Here we show, using in silico and in vivo analyses of mitogen-activated protein ( MAP) kinase signalling, that Ras nanoclusters operate as sensitive switches, converting graded ligand inputs into fixed outputs of activated extracellular signal-regulated kinase ( ERK). By generating Ras nanoclusters in direct proportion to ligand input, cells build an analogue-digital analogue circuit relay that transmits a signal across the plasma membrane with high fidelity. Signal transmission is completely dependent on Ras spatial organization and fails if nanoclustering is abrogated. A requirement for high-fidelity signalling may explain the non-random distribution of other plasma membrane signalling complexes.
引用
收藏
页码:905 / U60
页数:31
相关论文
共 52 条
[21]   Lipid rafts: contentious only from simplistic standpoints [J].
Hancock, John F. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (06) :456-462
[22]   Subcellular localization determines MAP kinase signal output [J].
Harding, A ;
Tian, TH ;
Westbury, E ;
Frische, E ;
Hancock, JF .
CURRENT BIOLOGY, 2005, 15 (09) :869-873
[23]   Identification of residues and domains of Raf important for function in vivo and in vitro [J].
Harding, A ;
Hsu, V ;
Kornfeld, K ;
Hancock, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (46) :45519-45527
[24]   Single- and multiple-molecule dynamics of the signaling from H-Ras to cRaf-1 visualized on the plasma membrane of living cells [J].
Hibino, K ;
Watanabe, TM ;
Kozuka, J ;
Iwane, AH ;
Okada, T ;
Kataoka, T ;
Yanagida, T ;
Sako, Y .
CHEMPHYSCHEM, 2003, 4 (07) :748-753
[25]   Ultrasensitivity in the mitogen-activated protein kinase cascade [J].
Huang, CYF ;
Ferrell, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10078-10083
[26]   Protein phosphatases 1 and 2A promote Raf-1 activation by regulating 14-3-3 interactions [J].
Jaumot, M ;
Hancock, JF .
ONCOGENE, 2001, 20 (30) :3949-3958
[27]   Intramolecular dephosphorylation of ERK by MKP3 [J].
Kim, Y ;
Rice, AE ;
Denu, JM .
BIOCHEMISTRY, 2003, 42 (51) :15197-15207
[28]   Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions [J].
Kolch, W .
BIOCHEMICAL JOURNAL, 2000, 351 :289-305
[29]   Paradigm shift of the plasma membrane concept from the two-dimensional continuum fluid to the partitioned fluid: High-speed single-molecule tracking of membrane molecules [J].
Kusumi, A ;
Nakada, C ;
Ritchie, K ;
Murase, K ;
Suzuki, K ;
Murakoshi, H ;
Kasai, RS ;
Kondo, J ;
Fujiwara, T .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2005, 34 :351-U54
[30]   Scaffold proteins may biphasically affect the levels of mitogen-activated protein kinase signaling and reduce its threshold properties [J].
Levchenko, A ;
Bruck, J ;
Sternberg, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5818-5823