Transcriptional regulation of hepatitis B virus by nuclear hormone receptors is a critical determinant of viral tropism.
نویسندگان
چکیده
Hepatotropism is a prominent feature of hepatitis B virus (HBV) infection. Cell lines of nonhepatic origin do not independently support HBV replication. Here, we show that the nuclear hormone receptors, hepatocyte nuclear factor 4 and retinoid X receptor alpha plus peroxisome proliferator-activated receptor alpha, support HBV replication in nonhepatic cells by controlling pregenomic RNA synthesis, indicating these liver-enriched transcription factors control a unique molecular switch restricting viral tropism. In contrast, hepatocyte nuclear factor 3 antagonizes nuclear hormone receptor-mediated viral replication, demonstrating distinct regulatory roles for these liver-enriched transcription factors.
منابع مشابه
Mechanisms of Inhibition of Nuclear Hormone Receptor-Dependent Hepatitis B Virus Replication by Hepatocyte Nuclear Factor 3 †
The nuclear hormone receptors hepatocyte nuclear factor 4 (HNF4) and the retinoid X (RXR ) plus the peroxisome proliferator-activated receptor (PPAR ) heterodimer support hepatitis B virus (HBV) replication in nonhepatoma cells. Hepatocyte nuclear factor 3 (HNF3) inhibits nuclear hormone receptor-mediated viral replication. Inhibition of HBV replication by HNF3 is associated with the preferenti...
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Viral hepatitis is one of five infectional factors cause early death in all over the world. Every day at least one million people die because of viral hepatitis. Six hepatitis viruses have been known until now. They are A, B, C, D, E, G, and it is probable that at least two other kinds i.e. F, and H, will be known soon. Only hepatitis B is a DNA virus, and the others are RNA viruses. All viruse...
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عنوان ژورنال:
- Proceedings of the National Academy of Sciences of the United States of America
دوره 98 4 شماره
صفحات -
تاریخ انتشار 2001