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Identifying Inhibitors of the HBx-DDB1 Interaction Using a Split Luciferase Assay System
Published on: December 21, 2019
The metabolic activator FOXO1 binds hepatitis B virus DNA and activates its transcription
1Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel. amirsh@tasmc.health.gov.il
Abstract:
Hepatitis B virus (HBV) is a small DNA virus that targets the liver and infects humans worldwide. Recently we have shown that the metabolic regulator PGC-1alpha coactivates HBV transcription thereby rendering the virus susceptible to fluctuations in the nutritional status of the liver. PGC-1alpha coactivation of HBV is mediated through the liver-enriched nuclear receptor HNF4alpha and through another yet unknown transcription factor(s). Here we show that the forkhead transcription factor FOXO1, a known target for PGC-1alpha coactivation and a central mediator of glucose metabolism in the liver, binds HBV core promoter and activates its transcription. This activation is further enhanced in the presence of PGC-1alpha, implying that FOXO1 is a target for PGC-1alpha coactivation of HBV transcription. Thus, our results identify another key metabolic regulator as an activator of HBV transcription, thereby supporting the principle that HBV gene expression is regulated in a similar way to key hepatic metabolic genes.
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