HBx Regulation on HBV Pregenome Promoter in the Episomal Form Versus the Integrated Form.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Hui Ding, Shuang Hu, Huihui Zhu, Ziyang Liu, Yuan Li, Jianping Liu, Xiaofang Li, Shuangyin Han, Suofeng Sun
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引用次数: 0

Abstract

Background: Hepatitis B virus (HBV) genome structure is an incomplete closed double stranded circular DNA and it uses covalently closed circular DNA (cccDNA) as template for replication. To study the antiviral effect on different HBV replication forms, a stable cell line expressing HBV using Huh7 cells with shuttle plasmid to imitate the real HBV replication form was stablished. Unlike the HepG2.2.15 cells, the replication of HBV-expressing Huh7 cells present significant decrease after 9 days of interferon-α (IFN-α) treatment. This study aimed to verify whether hepatitis B virus X (HBx) epigenetic regulation by HBV promoter is affected by the DNA form and discuss the differences between the episomal form and the integrated form.

Material and methods: Huh7 cells were used with two different plasmids containing HBV genome to imitate HBV-expressing cells with the episomal form and the integrated form. Luciferase reporting system was used to determine the activation of the promoter after treatment with IFN-α with different concentrations and promoter regulation factor HBx. HBx-expressing plasmid was transfected to evaluate its effect on HBV replication in the episomal form. HBV DNA and pregenomic RNA (pgRNA) in HBx knockdown cell line was determined and HBx-expressing plasmid was transfected to evaluate its effect on HBx in the episomal form.

Results: The two cell lines were established successfully and used for further experiments after selection. IFN-α showed significant inhibition effect on HBV pregenome promoter in the episomal form DNA while was not observed in the integrated form. After HBx-expressing plasmid was transfected, HBV pregenome promoter activity was higher in the episomal form rather than the integrated form. HBx showed a concentration-dependant activation on HBV replication in the episomal form. HBx knockdown reduced HBV production and HBV concentration significantly increased after transfection by HBx-expressing plasmid.

Conclusions: HBx regulation effect on HBV pregenome promoter is influenced by the HBV genome form. The epigenetic regulation effect on HBV pregenome promoter is more active in the episomal form rather than the integrated form.

HBx对个体形式与整体形式的HBV前基因组启动子的调控。
背景:乙型肝炎病毒(Hepatitis B virus, HBV)基因组结构为不完全闭合双链环状DNA,以共价闭合环状DNA (covalently closed circular DNA, cccDNA)为模板进行复制。为了研究其对不同HBV复制形式的抗病毒作用,我们利用带穿梭质粒的Huh7细胞建立了一个稳定表达HBV的细胞系来模拟HBV的真实复制形式。与HepG2.2.15细胞不同的是,在干扰素-α (IFN-α)处理9天后,表达hbv的Huh7细胞的复制明显减少。本研究旨在验证HBV启动子对乙型肝炎病毒X (HBx)的表观遗传调控是否受DNA形式的影响,并探讨片段形式与整合形式的差异。材料与方法:将Huh7细胞与两种不同的含HBV基因组的质粒结合,模拟体外表达HBV的细胞,分别为外体形式和整体形式。采用荧光素酶报告系统测定不同浓度IFN-α和启动子调节因子HBx处理后启动子的活化情况。转染表达hbx的质粒,以评估其对外体形式HBV复制的影响。测定HBx敲除细胞株的HBV DNA和基因组前RNA (pgRNA),并转染表达HBx的质粒,以评估其对episomal形式HBx的影响。结果:两株细胞系均成功建立,经筛选后可用于进一步实验。IFN-α对episomal形式DNA的HBV前基因组启动子有显著的抑制作用,而在整合形式DNA中没有观察到。表达hbx的质粒转染后,HBV前基因组启动子活性在个体形式高于整体形式。HBx表现出浓度依赖性的HBV复制激活。表达HBx的质粒转染后,HBx基因敲除降低了HBV的产生,HBV浓度显著升高。结论:HBx对HBV前基因组启动子的调控作用受HBV基因组形态的影响。对HBV前基因组启动子的表观遗传调控作用以表观小体形式比整体形式更为活跃。
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来源期刊
Discovery medicine
Discovery medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
5.40
自引率
0.00%
发文量
80
审稿时长
6-12 weeks
期刊介绍: Discovery Medicine publishes novel, provocative ideas and research findings that challenge conventional notions about disease mechanisms, diagnosis, treatment, or any of the life sciences subjects. It publishes cutting-edge, reliable, and authoritative information in all branches of life sciences but primarily in the following areas: Novel therapies and diagnostics (approved or experimental); innovative ideas, research technologies, and translational research that will give rise to the next generation of new drugs and therapies; breakthrough understanding of mechanism of disease, biology, and physiology; and commercialization of biomedical discoveries pertaining to the development of new drugs, therapies, medical devices, and research technology.
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