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The TSC1 tumour suppressor hamartin regulates cell adhesion through ERM proteins and the GTPase Rho.

Nature cell biology | May 2, 2000

http://www.ncbi.nlm.nih.gov/pubmed/10806479

Loss of the tumour-suppressor gene TSC1 is responsible for hamartoma development in tuberous sclerosis complex (TSC), which renders several organs susceptible to benign tumours. Hamartin, the protein encoded by TSC1, contains a coiled-coil domain and is expressed in most adult tissues, although its function is unknown. Here we show that hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins. Inhibition of hamartin function in cells containing focal adhesions results in loss of adhesion to the cell substrate, whereas overexpression of hamartin in cells lacking focal adhesions results in activation of the small GTP-binding protein Rho, assembly of actin stress fibres and formation of focal adhesions. Interaction of endogenous hamartin with ERM-family proteins is required for activation of Rho by serum or by lysophosphatidic acid (LPA). Our data indicate that disruption of adhesion to the cell matrix through loss of hamartin may initiate the development of TSC hamartomas and that a Rho-mediated signalling pathway regulating cell adhesion may constitute a rate-limiting step in tumour formation.

Pubmed ID: 10806479 RIS Download

Mesh terms: 3T3 Cells | Actins | Animals | Blood Proteins | Cell Adhesion | Cytoskeletal Proteins | Endothelium, Vascular | Enzyme Activation | Genes, Tumor Suppressor | Humans | Lysophospholipids | Membrane Proteins | Mice | Microfilament Proteins | Peptide Fragments | Phosphoproteins | Proteins | Signal Transduction | Stress, Mechanical | Tumor Suppressor Proteins | Two-Hybrid System Techniques | Umbilical Veins | rho GTP-Binding Proteins

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