the hepatitis e virus orf3 protein regulates the expression of liver-specific genes by modulating localization of hepatocyte nuclear factor 4戊肝病毒orf3蛋白质调节肝脏特异性基因的表达,调节肝细胞的核因子4的本地化.pdfVIP
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the hepatitis e virus orf3 protein regulates the expression of liver-specific genes by modulating localization of hepatocyte nuclear factor 4戊肝病毒orf3蛋白质调节肝脏特异性基因的表达,调节肝细胞的核因子4的本地化
The Hepatitis E Virus ORF3 Protein Regulates the
Expression of Liver-Specific Genes by Modulating
Localization of Hepatocyte Nuclear Factor 4
1 1 1 2 2
Vivek Chandra , Prasida Holla , Dhrubaa Ghosh , Debarshi Chakrabarti , Muralidhara Padigaru , Shahid
Jameel1*
1Virology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India, 2 Department of Biomarker Discovery, Piramal
Life Sciences Limited, Mumbai, India
Abstract
The hepatitis E virus (HEV) is a small RNA virus and the cause of acute viral hepatitis E. The open reading frame 3 protein
(pORF3) of HEV appears to be a pleiotropic regulatory protein that helps in the establishment, propagation and progression
of viral infection. However, the global cellular effects of this protein remain to be explored. In the absence of traditional in
vitro viral infection systems or efficient replicon systems, we made an adenovirus based ORF3 protein expression system to
study its effects on host cell gene expression. We infected Huh7 hepatoma cells with recombinant adenoviruses expressing
pORF3 and performed microarray-based gene expression analyses. Several genes down regulated in pORF3-expressing cells
were found to be under regulation of the liver-enriched hepatocyte nuclear factor 4 (HNF4), which regulates hepatocyte-
specific gene expression. While HNF4 localizes to the nucleus, its phosphorylation results in impaired nuclear localization of
HNF4. Here we report that pORF3 increases HNF4 phosphorylation through the ERK and Akt kinases, which results in
impaired nuclear translocation of HNF4 and subsequently the down modulation of HNF4-responsive genes in pORF3-
expressing cells. We propose that modulation of several hepa
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