PI3K-Akt signaling pathway upregulates hepatitis C virus RNA translation through the activation of SREBPs

Virology. 2016 Mar:490:99-108. doi: 10.1016/j.virol.2016.01.012. Epub 2016 Feb 6.

Abstract

Hepatitis C virus (HCV) activates PI3K-Akt signaling to enhance entry and replication. Here, we found that this pathway also increased HCV translation. Knocking down the three Akt isoforms significantly decreased, whereas ectopic expression increased HCV translation. HCV translation upregulation by Akt required their kinase activities because Akt kinase-dead mutants downregulated HCV translation; and was dependent on PI3K activity since it was sensitive to PI3K inhibitor wortmannin. The viral 3'UTR was not involved in translation upregulation by Akt. HCV NS5A increased Akt phosphorylation/activity and HCV translation in the absence of the viral 3'UTR. Sterol regulatory element-binding proteins (SREBPs) were the downstream effectors of the PI3K-Akt pathway in regulating HCV translation because Akt1 and Akt2 activated both SREBP-1 and SREBP-2, whereas Akt3 upregulated SREBP-1. Knocking down SREBPs significantly decreased, while ectopic expression of SREBPs increased HCV translation. Taken together, we showed that the PI3K-Akt signaling pathway positively regulates HCV translation through SREBPs.

Keywords: Akt isoforms; HCV RNA translation modulation; Hepatitis C virus (HCV); NS5A; PI3K; SREBPs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hepacivirus / genetics*
  • Hepacivirus / metabolism
  • Hepatitis C / enzymology
  • Hepatitis C / genetics
  • Hepatitis C / metabolism*
  • Hepatitis C / virology
  • Host-Pathogen Interactions
  • Humans
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • RNA, Viral / genetics*
  • RNA, Viral / metabolism
  • Signal Transduction
  • Sterol Regulatory Element Binding Protein 1 / genetics
  • Sterol Regulatory Element Binding Protein 1 / metabolism*
  • Sterol Regulatory Element Binding Protein 2 / genetics
  • Sterol Regulatory Element Binding Protein 2 / metabolism*
  • Up-Regulation

Substances

  • RNA, Viral
  • SREBF1 protein, human
  • SREBF2 protein, human
  • Sterol Regulatory Element Binding Protein 1
  • Sterol Regulatory Element Binding Protein 2
  • Phosphatidylinositol 3-Kinases
  • AKT1 protein, human
  • AKT2 protein, human
  • AKT3 protein, human
  • Proto-Oncogene Proteins c-akt