The Nuclear RhoA Exchange Factor Net1 Interacts with Proteins of the Dlg Family, Affects Their Localization, and Influences Their Tumor Suppressor Activity
| Autor: | Lisa Sharek, Rafael Garcia-Mata, Adi D. Dubash, Keith Burridge, Jeffrey A. Frost, Heather S. Carr |
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| Rok vydání: | 2007 |
| Předmět: |
RHOA
Oncogene Proteins Amino Acid Motifs Molecular Sequence Data Nuclear Localization Signals PDZ domain PDZ Domains Nerve Tissue Proteins Plasma protein binding Biology Discs Large Homolog 1 Protein Mice Cytosol Animals Guanine Nucleotide Exchange Factors Humans Amino Acid Sequence Molecular Biology Sequence Deletion Cell Nucleus Tumor Suppressor Proteins Neuropeptides Intracellular Signaling Peptides and Proteins Membrane Proteins Articles Cell Biology Rats SAP90-PSD95 Associated Proteins Transport protein Cell biology Enzyme Activation Protein Transport Cell Transformation Neoplastic Membrane protein Biochemistry DLG1 NIH 3T3 Cells biology.protein Guanine nucleotide exchange factor rhoA GTP-Binding Protein Disks Large Homolog 4 Protein HeLa Cells Protein Binding |
| Zdroj: | Molecular and Cellular Biology. 27:8683-8697 |
| ISSN: | 1098-5549 |
| Popis: | Net1 is a RhoA-specific guanine nucleotide exchange factor which localizes to the nucleus at steady state. A deletion in its N terminus redistributes the protein to the cytosol, where it activates RhoA and can promote transformation. Net1 contains a PDZ-binding motif at the C terminus which is essential for its transformation properties. Here, we found that Net1 interacts through its PDZ-binding motif with tumor suppressor proteins of the Dlg family, including Dlg1/SAP97, SAP102, and PSD95. The interaction between Net1 and its PDZ partners promotes the translocation of the PDZ proteins to nuclear subdomains associated with PML bodies. Interestingly, the oncogenic mutant of Net1 is unable to shuttle the PDZ proteins to the nucleus, although these proteins still associate as clusters in the cytosol. Our results suggest that the ability of oncogenic Net1 to transform cells may be in part related to its ability to sequester tumor suppressor proteins like Dlg1 in the cytosol, thereby interfering with their normal cellular function. In agreement with this, the transformation potential of oncogenic Net1 is reduced when it is coexpressed with Dlg1 or SAP102. Together, our results suggest that the interaction between Net1 and Dlg1 may contribute to the mechanism of Net1-mediated transformation. |
| Databáze: | OpenAIRE |
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