Hepatitis C Virus Induces E6AP-Dependent Degradation of the Retinoblastoma Protein
| Autor: | Jon M. Huibregtse, Yuqiong Liang, Seungtaek Kim, Stanley M. Lemon, Tsubasa Munakata, Akio Nomoto, David R. McGivern |
|---|---|
| Rok vydání: | 2007 |
| Předmět: |
Small interfering RNA
Hepatocellular carcinoma Hepacivirus Viral Nonstructural Proteins medicine.disease_cause Retinoblastoma Protein Hepatitis chemistry.chemical_compound 0302 clinical medicine RNA interference Tumor Cells Cultured Biology (General) 0303 health sciences Retinoblastoma protein virus diseases 3. Good health Infectious Diseases Oncology RNA polymerase 030220 oncology & carcinogenesis Viruses RNA Interference biological phenomena cell phenomena and immunity Research Article Proteasome Endopeptidase Complex Carcinoma Hepatocellular QH301-705.5 Ubiquitin-Protein Ligases Hepatitis C virus Immunology Down-Regulation RNA-dependent RNA polymerase Gastroenterology and Hepatology Biology Microbiology 03 medical and health sciences Virology Genetics medicine Humans E2F Molecular Biology NS5B 030304 developmental biology Ubiquitin Cell Biology RC581-607 RNA-Dependent RNA Polymerase digestive system diseases Proteasome chemistry ubiqutin ligase Cancer research biology.protein Parasitology Immunologic diseases. Allergy |
| Zdroj: | PLoS Pathogens PLoS Pathogens, Vol 3, Iss 9, Pp 1335-1347 (2007) |
| ISSN: | 1553-7374 |
| Popis: | Hepatitis C virus (HCV) is a positive-strand RNA virus that frequently causes persistent infections and is uniquely associated with the development of hepatocellular carcinoma. While the mechanism(s) by which the virus promotes cancer are poorly defined, previous studies indicate that the HCV RNA-dependent RNA polymerase, nonstructural protein 5B (NS5B), forms a complex with the retinoblastoma tumor suppressor protein (pRb), targeting it for degradation, activating E2F-responsive promoters, and stimulating cellular proliferation. Here, we describe the mechanism underlying pRb regulation by HCV and its relevance to HCV infection. We show that the abundance of pRb is strongly downregulated, and its normal nuclear localization altered to include a major cytoplasmic component, following infection of cultured hepatoma cells with either genotype 1a or 2a HCV. We further demonstrate that this is due to NS5B-dependent ubiquitination of pRb and its subsequent degradation via the proteasome. The NS5B-dependent ubiquitination of pRb requires the ubiquitin ligase activity of E6-associated protein (E6AP), as pRb abundance was restored by siRNA knockdown of E6AP or overexpression of a dominant-negative E6AP mutant in cells containing HCV RNA replicons. E6AP also forms a complex with pRb in an NS5B-dependent manner. These findings suggest a novel mechanism for the regulation of pRb in which the HCV NS5B protein traps pRb in the cytoplasm, and subsequently recruits E6AP to this complex in a process that leads to the ubiquitination of pRb. The disruption of pRb/E2F regulatory pathways in cells infected with HCV is likely to promote hepatocellular proliferation and chromosomal instability, factors important for the development of liver cancer. Author Summary Persons infected with hepatitis C virus (HCV) are at increased risk for liver cancer. This is remarkable because HCV is an RNA virus with replication confined to the cytoplasm and no potential for integration of its genome into host cell DNA. While it is likely that chronic inflammation contributes to liver cancer, prior studies with HCV transgenic mice indicate that the viral proteins are intrinsically carcinogenic. In this study, we have examined the interaction of one of these, the RNA-dependent RNA polymerase nonstructural protein 5B, with an important cellular tumor suppressor protein, the retinoblastoma protein (pRb). pRb is a master regulator of the cell cycle, and altered expression of some of the many genes it regulates may lead to cancer. We show that the abundance of pRb is strongly downregulated in cells infected with HCV, and that nonstructural protein 5B targets pRb for destruction via the cell's normal protein degradation machinery. The E6-associated protein appears to play a role in this process, which is interesting as it also mediates the degradation of another tumor suppressor, p53, by papillomaviruses. The loss of pRb function in HCV-infected cells likely promotes hepatocellular proliferation as well chromosomal instability, factors important for the development of liver cancer. |
| Databáze: | OpenAIRE |
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