N-terminal HCV core protein fragment decreases 20S proteasome activity in the presence of PA28γ

The Hepatitis C virus (HCV) core protein plays a crucial role in the development of chronic liver diseases such as chronic hepatitis, cirrhosis, and hepatocellular carcinoma (HCC). Its involvement in these diseases is reportedly abolished by a knockout of the proteasome activator PA28 gamma gene in transgenic mice, suggesting an interaction between the core protein and the PA28 gamma-proteasome system. This study found a direct interaction between the N-terminal 1-71 fragment of HCV core protein (Core71) and PA28 gamma in vitro, and that this interaction was found to enhance PA28 gamma-20S proteasome complex formation. While 20S proteasome activity was increased by PA28 gamma, it was significantly reduced by Core71 attachment in a dose-dependent manner. These results suggest that the Core-PA28 gamma interaction has an important role in regulating 20S proteasome activity and furthers our understanding of the pathogenesis of HCV. (C) 2018 Elsevier Inc. All rights reserved.