USP15 Participates in Hepatitis C Virus Propagation through Regulation of Viral RNA Translation and Lipid Droplet Formation

Shinji Kusakabe(The University of Osaka), Tatsuya Suzuki(Hamamatsu University School of Medicine), Yukari Sugiyama(The University of Osaka), Saori Haga(The University of Osaka), Kanako Horike(The University of Osaka), Makoto Tokunaga(The University of Osaka), Junki Hirano(The University of Osaka), He Zhang(The University of Osaka), David Virya Chen(The University of Osaka), Hanako Ishiga(The University of Osaka), Yasumasa Komoda(The University of Osaka), Chikako Ono(The University of Osaka), Takasuke Fukuhara(The University of Osaka), Masahiro Yamamoto(The University of Osaka), Masahito Ikawa(The University of Osaka), Takashi Satoh(The University of Osaka), Shizuo Akira(The University of Osaka), Tomohisa Tanaka(University of Yamanashi), Kohji Moriishi(University of Yamanashi), Moto Fukai(Hokkaido University), Akinobu Taketomi(Hokkaido University), Sachiyo Yoshio(National Center for Global Health and Medicine), Tatsuya Kanto(National Center for Global Health and Medicine), Tetsuro Suzuki(Hamamatsu University School of Medicine), Toru Okamoto(The University of Osaka), Yoshiharu Matsuura(The University of Osaka)
Journal of Virology
January 9, 2019
Cited by 27Open Access
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Abstract

Although ubiquitination has been shown to play important roles in the HCV life cycle, the roles of deubiquitinating enzymes (DUBs), which cleave ubiquitin chains from their substrates, in HCV propagation have not been investigated. Here, we identified USP15 as a DUB regulating HCV propagation. USP15 showed no interaction with viral proteins and no participation in innate immune responses. Deficiency of USP15 in Huh7 cells resulted in suppression of the translation of HCV RNA and reduction in the amounts of lipid droplets, and the addition of fatty acids partially restored the production of infectious HCV particles. These data suggest that USP15 participates in HCV propagation in hepatic cells through the regulation of viral RNA translation and lipid metabolism.


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