GOLT1B Activation in Hepatitis C Virus-Infected Hepatocytes Links ER Trafficking and Viral Replication.
Jacqueline ButterworthDamien GrégoireMarion PeterArmando Andres Roca SuarezGuillaume DesandréYannick SimoninAlessia VirzìAmal Zine El AabidineMarine GuivarchJean-Christophe AndrauEdouard BertrandEric AssenatJoachim LupbergerUrszula HibnerPublished in: Pathogens (Basel, Switzerland) (2021)
Chronic hepatitis C carries a high risk of development of hepatocellular carcinoma (HCC), triggered by both direct and indirect effects of the virus. We examined cell-autonomous alterations in gene expression profiles associated with hepatitis C viral presence. Highly sensitive single molecule fluorescent in situ hybridization applied to frozen tissue sections of a hepatitis C patient allowed the delineation of clusters of infected hepatocytes. Laser microdissection followed by RNAseq analysis of hepatitis C virus (HCV)-positive and -negative regions from the tumoral and non-tumoral tissues from the same patient revealed HCV-related deregulation of expression of genes in the tumor and in the non-tumoral tissue. However, there was little overlap between both gene sets. Our interest in alterations that increase the probability of tumorigenesis prompted the examination of genes whose expression was increased by the virus in the non-transformed cells and whose level remained high in the tumor. This strategy led to the identification of a novel HCV target gene: GOLT1B, which encodes a protein involved in ER-Golgi trafficking. We further show that GOLT1B expression is induced during the unfolded protein response, that its presence is essential for efficient viral replication, and that its expression is correlated with poor outcome in HCC.
Keyphrases
- hepatitis c virus
- poor prognosis
- human immunodeficiency virus
- genome wide
- single molecule
- binding protein
- genome wide identification
- sars cov
- copy number
- endoplasmic reticulum
- case report
- induced apoptosis
- long non coding rna
- bioinformatics analysis
- genome wide analysis
- stem cells
- endoplasmic reticulum stress
- transcription factor
- atomic force microscopy
- mesenchymal stem cells
- amino acid
- quantum dots
- cell death
- high speed
- cell cycle arrest
- label free
- tandem mass spectrometry