Hepatitis B virus Core protein nuclear interactome identifies SRSF10 as a host RNA-binding protein restricting HBV RNA production

Author:

Chabrolles HélèneORCID,Auclair Héloïse,Vegna Serena,Lahlali ThomasORCID,Pons Caroline,Michelet Maud,Couté Yohann,Belmudes Lucid,Chadeuf GillianeORCID,Kim YujinORCID,Di Bernardo Ariel,Jalaguier Pascal,Cosset François-LoïcORCID,Fusil FlorianeORCID,Rivoire Michel,Arnold Lee D.ORCID,Lopatin UriORCID,Combet Christophe,Zoulim FabienORCID,Grierson DavidORCID,Chabot BenoitORCID,Lucifora Julie,Durantel DavidORCID,Salvetti AnnaORCID

Abstract

Despite the existence of a preventive vaccine, chronic infection with Hepatitis B virus (HBV) affects more than 250 million people and represents a major global cause of hepatocellular carcinoma (HCC) worldwide. Current clinical treatments, in most of cases, do not eliminate viral genome that persists as a DNA episome in the nucleus of hepatocytes and constitutes a stable template for the continuous expression of viral genes. Several studies suggest that, among viral factors, the HBV core protein (HBc), well-known for its structural role in the cytoplasm, could have critical regulatory functions in the nucleus of infected hepatocytes. To elucidate these functions, we performed a proteomic analysis of HBc-interacting host-factors in the nucleus of differentiated HepaRG, a surrogate model of human hepatocytes. The HBc interactome was found to consist primarily of RNA-binding proteins (RBPs), which are involved in various aspects of mRNA metabolism. Among them, we focused our studies on SRSF10, a RBP that was previously shown to regulate alternative splicing (AS) in a phosphorylation-dependent manner and to control stress and DNA damage responses, as well as viral replication. Functional studies combining SRSF10 knockdown and a pharmacological inhibitor of SRSF10 phosphorylation (1C8) showed that SRSF10 behaves as a restriction factor that regulates HBV RNAs levels and that its dephosphorylated form is likely responsible for the anti-viral effect. Surprisingly, neither SRSF10 knock-down nor 1C8 treatment modified the splicing of HBV RNAs but rather modulated the level of nascent HBV RNA. Altogether, our work suggests that in the nucleus of infected cells HBc interacts with multiple RBPs that regulate viral RNA metabolism. Our identification of SRSF10 as a new anti-HBV restriction factor offers new perspectives for the development of new host-targeted antiviral strategies.

Funder

Institut National de la Santé et de la Recherche Médicale

Centre National de la Recherche Scientifique

Université Claude Bernard Lyon 1

Canadian Institutes of Health Research

Assembly Biosciences

Agence Nationale de Recherche sur le Sida et les hépatites virales

FINOVI

Agence Nationale de la Recherche

Publisher

Public Library of Science (PLoS)

Subject

Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology

Reference104 articles.

1. Mechanisms of HBV-induced hepatocellular carcinoma;M Levrero;J Hepatol,2016

2. Antiviral therapies and prospects for a cure of chronic hepatitis B;F Zoulim;Cold Spring Harb Perspect Med,2015

3. Towards an HBV cure: state-of-the-art and unresolved questions—report of the ANRS workshop on HBV cure;MB Zeisel;Gut,2015

4. New antiviral targets for innovative treatment concepts for hepatitis B virus and hepatitis delta virus;D Durantel;J Hepatol,2016

5. Therapeutic strategies for hepatitis B virus infection: towards a cure.;GC Fanning;Nat Rev Drug Discov,2019

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3