首页> 外文期刊>Oncogenesis. >Initial sites of hepadnavirus integration into host genome in human hepatocytes and in the woodchuck model of hepatitis B-associated hepatocellular carcinoma
【24h】

Initial sites of hepadnavirus integration into host genome in human hepatocytes and in the woodchuck model of hepatitis B-associated hepatocellular carcinoma

机译:Hepadnavirus的初始位点在人肝细胞中的宿主基因组和甲型肝炎相关肝细胞癌的木质妥麦麦麦克库模型中

获取原文
           

摘要

Hepatitis B virus (HBV) and the closely related woodchuck hepatitis virus (WHV) are potent carcinogens that trigger development of primary hepatocellular carcinoma (HCC). The initial sites of hepadnavirus–host genome integration, their diversity and kinetics of formation can be central to virus persistence and the initiation and progression of HCC. To recognize the nature of the very early virus–host interactions, we explored de novo infection of human hepatocyte-like HepaRG cells with authentic HBV and naive woodchucks with WHV. HepaRG were analyzed from several minutes post exposure to HBV onwards, whereas woodchuck liver biopsies at 1 or 3?h and 6 weeks post infection with WHV. Inverse PCR and clonal sequencing of the amplicons were applied to identify virus–host genomic junctions. HBV and WHV DNA and their replication intermediates became detectable in one hour after virus exposure. Concomitantly, HBV DNA integration into various host genes was detected. Notably, junctions of HBV X gene with retrotransposon sequences, such as LINE1 and LINE2, became prominent shortly after infection. In woodchucks, insertion of WHV X and preS sequences into host genome was evident at 1 and 3?h post infection (h.p.i.), confirming that hepadnavirus under natural conditions integrates into hepatocyte DNA soon after invasion. The HBV and WHV X gene enhancer II/core promotor sequence most often formed initial junctions with host DNA. Moreover, multiple virus–virus DNA fusions appeared from 1?h.p.i. onwards in both infected hepatocytes and woodchuck livers. In summary, HBV DNA integrates almost immediately after infection with a variety of host’s sequences, among which tandemly repeating non-coding DNAs are common. This study revealed that HBV can engage mobile genetic elements from the beginning of infection to induce pro-oncogenic perturbations throughout the host genome. Such swift virus insertion was also evident in natural hepadnaviral infection in woodchucks.
机译:乙型肝炎病毒(HBV)和密切相关的木质耳肝炎病毒(WHV)是有效的致癌物,其引发原发性肝细胞癌(HCC)的发育。 Hepadnavirus-host基因组集成的初始位点,它们的多样性和形成动力学可以是病毒持久性的核心和HCC的启动和进展。为了认识到早期病毒宿主相互作用的性质,我们探讨了具有与WHV的真正的HBV和天真的木质刮擦人类肝细胞样肝细胞的Novo感染。分析了从接触HBV的几分钟后分析了肝脏,而用1或3μl的木质碰肝活组织检查,并且在WHV的感染后6周。逆PCR和扩增子的克隆测序被应用于鉴定病毒 - 宿主基因组结。 HBV和WHV DNA及其复制中间体在病毒暴露后1小时内可检测到可检测。同时,检测到HBV DNA集成到各种宿主基因中。值得注意的是,HBV X基因与Retroxposon序列(例如Line1和Line2)的连接,感染后不久性变得突出。在啄木枝中,在感染后1和3℃(H.P.I.)中,将WHV X和PRES序列插入到宿主基因组中,确认在侵袭后很快将肝病病毒整合到肝细胞DNA中。 HBV和WHV X基因增强剂II /核心促进序列最常形成初始结具有宿主DNA。此外,多种病毒病毒DNA融合出现在1℃下。在感染的肝细胞和啄木枝肝脏。总之,HBV DNA几乎立即通过多种宿主的序列感染,其中串联重复非编码DNA是常见的。该研究表明,HBV可以从感染开始时从事流动遗传元素,以诱导整个宿主基因组的雌性扰动。这种Swift病毒插入在伍德省的天然肝脏感染中也显而易见。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号