Growth factor receptor-bound protein 2, also known as Grb2, is an adaptor protein involved in signal transduction/cell communication. In humans, the GRB2 protein is encoded by the GRB2 gene.[5][6]
The protein encoded by this gene binds receptors such as the epidermal growth factor receptor and contains one SH2 domain and two SH3 domains. Its two SH3 domains direct complex formation with proline-rich regions of other proteins, and its SH2 domain binds tyrosine phosphorylated sequences. This gene is similar to the sem-5 gene of Caenorhabditis elegans, which is involved in the signal transduction pathway. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene.[7]
Function and expression
editGrb2 is widely expressed and is essential for multiple cellular functions. Inhibition of Grb2 function impairs developmental processes in various organisms and blocks transformation and proliferation of various cell types. It is thus not surprising that targeted gene disruption of Grb2 in mice is lethal at an early embryonic stage. Grb2 is best known for its ability to link the epidermal growth factor receptor tyrosine kinase to the activation of Ras and its downstream kinases, ERK1,2. Grb2 is composed of an SH2 domain flanked on each side by an SH3 domain. Grb2 has two closely related proteins with similar domain organizations, Gads and Grap. Gads and Grap are expressed specifically in hematopoietic cells and function in the coordination of tyrosine kinase mediated signal transduction.
Domains
editThe SH2 domain of Grb2 binds to phosphorylated tyrosine-containing peptides on receptors or scaffold proteins with a preference for pY-X-N-X, where X is generally a hydrophobic residue such as valine (see [1]).
The N-terminal SH3 domain binds to proline-rich peptides and can bind to the Ras-guanine exchange factor SOS.
The C-terminal SH3 domain binds to peptides conforming to a P-X-I/L/V/-D/N-R-X-X-K-P motif that allows it to specifically bind to proteins such as Gab-1.[8]
Interactions
editGrb2 has been shown to interact with:
- ADAM15,[9]
- Abl gene,[10][11]
- Arachidonate 5-lipoxygenase,[12][13]
- B-cell linker,[14][15][16][17]
- BCAR1,[18][19]
- BCR gene,[20][21][22][23][24][25]
- Beta-2 adrenergic receptor,[26]
- C-Met,[27][28]
- CBLB,[29][30][31]
- CD117,[32][33][34]
- CD22,[35][36]
- CD28,[37][38]
- CDKN1B,[39]
- CRK,[40][41][42]
- Cbl gene,[29][43][44][45][46][47][48][49][50][51][52][53][54]
- Colony stimulating factor 1 receptor,[55]
- DCTN1,[56]
- DNM1,[57][58]
- Dock180,[59][60]
- Dystroglycan,[61]
- EPH receptor A2,[62]
- ETV6,[20]
- Epidermal growth factor receptor,[6][63][64][65][66][67][68][69][70][71]
- Erythropoietin receptor,[32][72]
- FRS2,[44][73][74][75]
- Fas ligand,[76][77]
- GAB1,[63][78][79]
- GAB2,[20][80][81]
- Glycoprotein 130,[82]
- Granulocyte colony-stimulating factor receptor,[83]
- HER2/neu,[65][84][85]
- HNRNPC,[86]
- Huntingtin,[87]
- INPP5D,[88]
- IRS1,[89][90][91]
- ITK,[92][93]
- Janus kinase 1,[89][94]
- Janus kinase 2,[89][95]
- KHDRBS1,[46][63][96]
- Linker of activated T cells,[97][98][99]
- Lymphocyte cytosolic protein 2,[43][78][100][101][102]
- MAP2,[103][104]
- MAP3K1[105]
- MAP4K1,[106][107][108][109]
- MED28,[110]
- MST1R,[111][112]
- MUC1,[113]
- Mitogen-activated protein kinase 9,[114][115]
- NCKIPSD,[116][117]
- NEU3,[118]
- PDGFRB,[71][119][120]
- PIK3R1,[121][122]
- PLCG1,[123][124][125]
- PRKAR1A,[68]
- PTK2,[18][126][127][128][129]
- PTPN11,[83][120][130][131][132][133][134][135][136]
- PTPN12,[137]
- PTPN1,[138][139]
- PTPN6,[45][131][140]
- PTPRA,[141][142][143]
- RAPGEF1,[144][145]
- RET proto-oncogene,[146][147]
- SH2B1,[148][149]
- SH3KBP1,[150][151]
- SHC1,[21][45][47][64][90][130][152][153][154][155][156][157][158][159][160][161][162][163][164][165][166]
- SOS1,[21][42][44][45][46][47][58][63][64][70][100][113][124][158][165][167][168][169][170][171][172]
- Src,[45][173]
- Syk,[45][131]
- TNK2,[152][174]
- TrkA,[175][176]
- VAV1,[82][167][177][178]
- VAV2,[64][84]
- VAV3,[64][179] and
- Wiskott-Aldrich syndrome protein.[180][181]
See also
editReferences
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Further reading
edit- Colledge M, Froehner SC (May 1998). "Interaction between the nicotinic acetylcholine receptor and Grb2. Implications for signaling at the neuromuscular junction". Annals of the New York Academy of Sciences. 841 (1): 17–27. Bibcode:1998NYASA.841...17C. doi:10.1111/j.1749-6632.1998.tb10907.x. PMID 9668219. S2CID 41992031.
- Ramesh N, Antón IM, Martínez-Quiles N, Geha RS (January 1999). "Waltzing with WASP". Trends in Cell Biology. 9 (1): 15–9. doi:10.1016/S0962-8924(98)01411-1. PMID 10087612.
- O'Sullivan E, Kinnon C, Brickell P (1999). "Wiskott-Aldrich syndrome protein, WASP". The International Journal of Biochemistry & Cell Biology. 31 (3–4): 383–7. doi:10.1016/S1357-2725(98)00118-6. PMID 10224664.
- Schlaepfer DD, Hauck CR, Sieg DJ (1999). "Signaling through focal adhesion kinase". Progress in Biophysics and Molecular Biology. 71 (3–4): 435–78. doi:10.1016/S0079-6107(98)00052-2. PMID 10354709.
- Vidal M, Liu WQ, Gril B, Assayag F, Poupon MF, Garbay C (2004). "[Design of new anti-tumor agents interrupting deregulated signaling pathways induced by tyrosine kinase proteins. Inhibition of protein-protein interaction involving Grb2]". Journal de la Société de Biologie. 198 (2): 133–7. doi:10.1051/jbio/2004198020133. PMID 15368963. S2CID 88696735.
External links
edit- GRB2+Adaptor+Protein at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- The Grb2 protein page on The SH2 Website
- GeneCards entry for Grb2
- Human Protein Resource Database entry for Grb2
- Grb2 information on iHOP (Information Hyperlinked over Proteins)
- GRB2 Info with links in the Cell Migration Gateway Archived December 11, 2014, at the Wayback Machine