| Literature DB >> 30563842 |
You Zhang1, Jing Lu1, Jing Ma1, Xinqi Liu2.
Abstract
Insulin-induced gene 1 (INSIG1) regulates sterol synthesis by mediating the activation of sterol regulatory element-binding protein (SREBP) and the degradation of the HMG-CoA reductase (HMGCR). INSIG1 is up-regulated during HIV-1 infection, but its role in HIV-1 infection is unknown. In this report, using pseudovirus production, protein overexpression, and gene knockouts, we found that INSIG1 inhibits HIV-1 production by accelerating the degradation of the HIV-1 Gag protein. Unlike the degradation of HMGCR via the E3 ubiquitin ligase autocrine motility factor receptor (AMFR), a process that depends on the proteasome, INSIG1 coordinated with another ligase, translocation in renal carcinoma chromosome 8 (TRC8), and promoted Gag degradation through the lysosome pathway. We conclude that INSIG1 functions as a sentinel responsive to HIV-1 production and inhibits HIV-1 replication by degrading Gag, a process occurring at intracellular membrane sites such as the endoplasmic reticulum and endosomes where both INSIG1 and Gag may be located.Entities:
Keywords: Gag protein; HIV replication; HIV-1 production; TRC8; endosome; insulin-induced gene 1 (INSIG1); lysosome pathway degradation; protein degradation; protein expression; ring finger protein 139 (RNF139); ubiquitin ligase; viral protein; virology; virus
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Year: 2018 PMID: 30563842 PMCID: PMC6369274 DOI: 10.1074/jbc.RA118.004630
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157