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阴阳 1 和 HBx 蛋白通过介导 cccDNA 微染色体与细胞染色体 19p13.11 的空间相互作用来激活 HBV 转录。

Yin-Yang 1 and HBx protein activate HBV transcription by mediating the spatial interaction of cccDNA minichromosome with cellular chromosome 19p13.11.

机构信息

State Key Laboratory of Natural and Biomimetic Drugs, Department of Microbiology & Infectious Disease Center, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, People's Republic of China.

Key Laboratory of Medical Molecular Virology (MOE & MOH), School of Basic Medical Sciences, Fudan University, Shanghai, People's Republic of China.

出版信息

Emerg Microbes Infect. 2020 Dec;9(1):2455-2464. doi: 10.1080/22221751.2020.1840311.

Abstract

HBV cccDNA stably exists in the nuclei of infected cells as an episomal munichromosome which is responsible for viral persistence and failure of current antiviral treatments. However, the regulatory mechanism of cccDNA transcription by viral and host cellular factors is not well understood. In this study, we investigated whether cccDNA could be recruited into a specific region of the nucleus via specific interaction with a cellular chromatin to regulate its transcription activity. To investigate this hypothesis, we used chromosome conformation capture (3C) technology to search for the potential interaction of cccDNA and cellular chromatin through rcccDNA transfection in hepatoma cells and found that cccDNA is specifically associated with human chromosome 19p13.11 region, which contains a highly active enhancer element. We also confirmed that cellular transcription factor Yin-Yang 1 (YY1) and viral protein HBx mediated the spatial regulation of HBV cccDNA transcription by 19p13.11 enhancer. Thus, These findings indicate that YY1 and HBx mediate the recruitment of HBV cccDNA minichromosomes to 19p13.11 region for transcription activation, and YY1 may present as a novel therapeutic target against HBV infection.

摘要

HBV cccDNA 作为一种游离于染色体外的单染色体,稳定存在于受感染细胞的核内,负责病毒的持续存在和当前抗病毒治疗的失败。然而,病毒和宿主细胞因子对 cccDNA 转录的调控机制尚不清楚。在这项研究中,我们研究了 cccDNA 是否可以通过与细胞染色质的特定相互作用,招募到特定的核区域,从而调节其转录活性。为了验证这一假说,我们使用染色体构象捕获(3C)技术,通过 rcccDNA 转染在肝癌细胞中寻找 cccDNA 和细胞染色质的潜在相互作用,发现 cccDNA 与包含高度活跃增强子元件的人类染色体 19p13.11 区域特异性相关。我们还证实,细胞转录因子 Yin-Yang 1(YY1)和病毒蛋白 HBx 通过 19p13.11 增强子介导 HBV cccDNA 转录的空间调节。因此,这些发现表明,YY1 和 HBx 介导 HBV cccDNA 微染色体募集到 19p13.11 区域以进行转录激活,并且 YY1 可能成为针对 HBV 感染的新型治疗靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23a3/7671595/209d2b3d646a/TEMI_A_1840311_F0001_OC.jpg

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