SENP3-mediated host defense response contains HBV replication and restores protein synthesis.

Journal Article (Journal Article)

Certain organs are capable of containing the replication of various types of viruses. In the liver, infection of Hepatitis B virus (HBV), the etiological factor of Hepatitis B and hepatocellular carcinoma (HCC), often remains asymptomatic and leads to a chronic carrier state. Here we investigated how hepatocytes contain HBV replication and promote their own survival by orchestrating a translational defense mechanism via the stress-sensitive SUMO-2/3-specific peptidase SENP3. We found that SENP3 expression level decreased in HBV-infected hepatocytes in various models including HepG2-NTCP cell lines and a humanized mouse model. Downregulation of SENP3 reduced HBV replication and boosted host protein translation. We also discovered that IQGAP2, a Ras GTPase-activating-like protein, is a key substrate for SENP3-mediated de-SUMOylation. Downregulation of SENP3 in HBV infected cells facilitated IQGAP2 SUMOylation and degradation, which leads to suppression of HBV gene expression and restoration of global translation of host genes via modulation of AKT phosphorylation. Thus, The SENP3-IQGAP2 de-SUMOylation axis is a host defense mechanism of hepatocytes that restores host protein translation and suppresses HBV gene expression.

Full Text

Duke Authors

Cited Authors

  • Xi, R; Kadur Lakshminarasimha Murthy, P; Tung, K-L; Guy, CD; Wan, J; Li, F; Wang, Z; Li, X; Varanko, A; Rakhilin, N; Xin, Y; Liu, B; Qian, S-B; Su, L; Han, Y; Shen, X

Published Date

  • 2019

Published In

Volume / Issue

  • 14 / 1

Start / End Page

  • e0209179 -

PubMed ID

  • 30640896

Pubmed Central ID

  • PMC6331149

Electronic International Standard Serial Number (EISSN)

  • 1932-6203

Digital Object Identifier (DOI)

  • 10.1371/journal.pone.0209179


  • eng

Conference Location

  • United States