Open AccessE6AP Ubiquitin Ligase Mediates Ubiquitylation and Degradation of Hepatitis C Virus Core Protein
Author(s) -
Masayuki Saijo,
Kyoko Murakami,
Tsuyoshi Ichimura,
Ritsuro Suzuki,
Tetsu Shimoji,
Kouichirou Fukuda,
Katsutoshi Abe,
Shota Sato,
Masayoshi Fukasawa,
Yoshio Yamakawa,
Masahiro Nishijima,
Kohji Moriishi,
Yoshiharu Matsuura,
Takaji Wakita,
Tetsuro Suzuki,
Peter M. Howley,
Tatsuo Miyamura,
Ikuo Shoji
Publication year - 2007
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01684-06
Subject(s) - biology , ubiquitin , ubiquitin ligase , gene knockdown , protein degradation , proteasome , hepatitis c virus , rna interference , microbiology and biotechnology , virology , rna , virus , biochemistry , gene
Hepatitis C virus (HCV) core protein is a major component of viral nucleocapsid and a multifunctional protein involved in viral pathogenesis and hepatocarcinogenesis. We previously showed that the HCV core protein is degraded through the ubiquitin-proteasome pathway. However, the molecular machinery for core ubiquitylation is unknown. Using tandem affinity purification, we identified the ubiquitin ligase E6AP as an HCV core-binding protein. E6AP was found to bind to the core protein in vitro and in vivo and promote its degradation in hepatic and nonhepatic cells. Knockdown of endogenous E6AP by RNA interference increased the HCV core protein level. In vitro and in vivo ubiquitylation assays showed that E6AP promotes ubiquitylation of the core protein. Exogenous expression of E6AP decreased intracellular core protein levels and supernatant HCV infectivity titers in the HCV JFH1-infected Huh-7 cells. Furthermore, knockdown of endogenous E6AP by RNA interference increased intracellular core protein levels and supernatant HCV infectivity titers in the HCV JFH1-infected cells. Taken together, our results provide evidence that E6AP mediates ubiquitylation and degradation of HCV core protein. We propose that the E6AP-mediated ubiquitin-proteasome pathway may affect the production of HCV particles through controlling the amounts of viral nucleocapsid protein.