• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Functional characterization of naturally occurring variants of human hepatitis B virus containing the core internal deletion mutation.含核心区内部缺失突变的人乙型肝炎病毒自然发生变异体的功能特性分析
J Virol. 1998 Mar;72(3):2168-76. doi: 10.1128/JVI.72.3.2168-2176.1998.
2
Out-of-frame versus in-frame core internal deletion variants of human and woodchuck hepatitis B viruses.人乙型肝炎病毒和土拨鼠乙型肝炎病毒的移码与框内核心内部缺失变异体
Virology. 2002 Jan 5;292(1):35-43. doi: 10.1006/viro.2001.1228.
3
Functional analysis of HBV genomes from patients with fulminant hepatitis.暴发性肝炎患者乙肝病毒基因组的功能分析
Hepatology. 1998 Nov;28(5):1390-7. doi: 10.1002/hep.510280530.
4
The replication phenotype of hepatitis B virus (HBV) splice variants Sp3 and Sp9 and their impact on wild-type HBV replication.乙型肝炎病毒(HBV)剪接变异体 Sp3 和 Sp9 的复制表型及其对野生型 HBV 复制的影响。
J Virol. 2024 Apr 16;98(4):e0153823. doi: 10.1128/jvi.01538-23. Epub 2024 Mar 19.
5
Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication.乙肝病毒核心启动子自然发生的突变对前核心基因表达及病毒复制的影响
J Virol. 1996 Sep;70(9):5845-51. doi: 10.1128/JVI.70.9.5845-5851.1996.
6
Type, prevalence, and significance of core promoter/enhancer II mutations in hepatitis B viruses from immunosuppressed patients with severe liver disease.免疫抑制的重症肝病患者乙型肝炎病毒核心启动子/增强子II突变的类型、流行率及意义
J Virol. 1996 Dec;70(12):8318-31. doi: 10.1128/JVI.70.12.8318-8331.1996.
7
Association between frequency of amino acid changes in core region of hepatitis B virus (HBV) and the presence of precore mutation in Japanese HBV carriers.日本乙肝病毒携带者中乙肝病毒核心区域氨基酸变化频率与前核心突变存在情况之间的关联
J Gastroenterol. 1997 Oct;32(5):611-22. doi: 10.1007/BF02934110.
8
Hepatitis B virus: prevalence of precore/core promoter mutants in different clinical categories of Indian patients.乙型肝炎病毒:印度患者不同临床类型中前核心/核心启动子突变体的流行情况。
J Viral Hepat. 2003 Sep;10(5):367-82. doi: 10.1046/j.1365-2893.2003.00445.x.
9
Persistence of Hepatitis B Virus DNA and the Tempos between Virion Secretion and Genome Maturation in a Mouse Model.在小鼠模型中乙型肝炎病毒 DNA 的持续性及其与病毒粒子分泌和基因组成熟之间的时间关系。
J Virol. 2019 Oct 29;93(22). doi: 10.1128/JVI.01001-19. Print 2019 Nov 15.
10
The mechanism of an immature secretion phenotype of a highly frequent naturally occurring missense mutation at codon 97 of human hepatitis B virus core antigen.人乙肝病毒核心抗原第97位密码子高频自然发生错义突变导致未成熟分泌表型的机制
J Virol. 1999 Jul;73(7):5731-40. doi: 10.1128/JVI.73.7.5731-5740.1999.

引用本文的文献

1
Low pathogenic avian influenza virus isolates with different levels of defective genome segments vary in pathogenicity and transmission efficiency.低致病性禽流感病毒分离株具有不同程度的缺陷基因组片段,其致病性和传播效率也有所不同。
Vet Res. 2020 Aug 28;51(1):108. doi: 10.1186/s13567-020-00833-6.
2
Persistence of Hepatitis B Virus DNA and the Tempos between Virion Secretion and Genome Maturation in a Mouse Model.在小鼠模型中乙型肝炎病毒 DNA 的持续性及其与病毒粒子分泌和基因组成熟之间的时间关系。
J Virol. 2019 Oct 29;93(22). doi: 10.1128/JVI.01001-19. Print 2019 Nov 15.
3
Inhibition of infection spread by co-transmitted defective interfering particles.共传播的缺陷干扰颗粒对感染传播的抑制作用。
PLoS One. 2017 Sep 15;12(9):e0184029. doi: 10.1371/journal.pone.0184029. eCollection 2017.
4
HBV polymerase overexpression due to large core gene deletion enhances hepatoma cell growth by binding inhibition of microRNA-100.由于核心大基因缺失导致的乙肝病毒聚合酶过表达通过抑制微小RNA-100的结合来增强肝癌细胞生长。
Oncotarget. 2016 Feb 23;7(8):9448-61. doi: 10.18632/oncotarget.7021.
5
Increased expression of Gp96 by HBx-induced NF-κB activation feedback enhances hepatitis B virus production.HBx 诱导的 NF-κB 激活反馈增强 Gp96 的表达,从而增强乙型肝炎病毒的产生。
PLoS One. 2013 Jun 11;8(6):e65588. doi: 10.1371/journal.pone.0065588. Print 2013.
6
Conformational changes in the hepatitis B virus core protein are consistent with a role for allostery in virus assembly.乙型肝炎病毒核心蛋白构象变化与变构在病毒组装中的作用一致。
J Virol. 2010 Feb;84(3):1607-15. doi: 10.1128/JVI.02033-09. Epub 2009 Nov 25.
7
Virologic characteristics of hepatitis B virus in patients infected via maternal-fetal transmission.经母婴传播感染的乙型肝炎病毒感染者的病毒学特征
World J Gastroenterol. 2008 Oct 7;14(37):5674-82. doi: 10.3748/wjg.14.5674.
8
Comparison of complete sequences of hepatitis B virus genotype C between inactive carriers and hepatocellular carcinoma patients before and after seroconversion.免疫血清转化前后,乙肝病毒C基因型完整序列在非活动性携带者与肝细胞癌患者之间的比较。
J Gastroenterol. 2007 Oct;42(10):837-44. doi: 10.1007/s00535-007-2100-6. Epub 2007 Oct 15.
9
A heteroaryldihydropyrimidine activates and can misdirect hepatitis B virus capsid assembly.一种杂芳基二氢嘧啶可激活并可能误导乙型肝炎病毒衣壳组装。
Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8138-43. doi: 10.1073/pnas.0409732102. Epub 2005 May 31.
10
Hepatitis B virus capsid assembly is enhanced by naturally occurring mutation F97L.自然发生的F97L突变增强了乙肝病毒衣壳组装。
J Virol. 2004 Sep;78(17):9538-43. doi: 10.1128/JVI.78.17.9538-9543.2004.

本文引用的文献

1
A defective interference-like phenomenon of human hepatitis B virus in chronic carriers.慢性乙肝携带者中人类乙型肝炎病毒的一种缺陷干扰样现象。
J Virol. 1998 Jan;72(1):578-84. doi: 10.1128/JVI.72.1.578-584.1998.
2
Novel and frequent mutations of hepatitis B virus coincide with a major histocompatibility complex class I-restricted T-cell epitope of the surface antigen.乙型肝炎病毒的新型频繁突变与表面抗原的主要组织相容性复合体I类限制性T细胞表位一致。
J Virol. 1997 Jun;71(6):4852-6. doi: 10.1128/JVI.71.6.4852-4856.1997.
3
Visualization of a 4-helix bundle in the hepatitis B virus capsid by cryo-electron microscopy.通过冷冻电子显微镜观察乙型肝炎病毒衣壳中的四螺旋束。
Nature. 1997 Mar 6;386(6620):91-4. doi: 10.1038/386091a0.
4
Determination of the fold of the core protein of hepatitis B virus by electron cryomicroscopy.通过电子冷冻显微镜测定乙型肝炎病毒核心蛋白的倍数。
Nature. 1997 Mar 6;386(6620):88-91. doi: 10.1038/386088a0.
5
Naturally occurring core-gene-defective hepatitis B viruses.
J Gen Virol. 1995 Jul;76 ( Pt 7):1821-6. doi: 10.1099/0022-1317-76-7-1821.
6
Hepadnavirus assembly and reverse transcription require a multi-component chaperone complex which is incorporated into nucleocapsids.嗜肝DNA病毒的组装和逆转录需要一种多组分伴侣蛋白复合物,该复合物会整合到核衣壳中。
EMBO J. 1997 Jan 2;16(1):59-68. doi: 10.1093/emboj/16.1.59.
7
Characterization of T-cell response to woodchuck hepatitis virus core protein and protection of woodchucks from infection by immunization with peptides containing a T-cell epitope.土拨鼠对土拨鼠肝炎病毒核心蛋白的T细胞反应特征以及通过用含T细胞表位的肽免疫来保护土拨鼠免受感染。
J Virol. 1997 Jan;71(1):65-74. doi: 10.1128/JVI.71.1.65-74.1997.
8
Accumulation and persistence of hepatitis B virus core gene deletion mutants in renal transplant patients are associated with end-stage liver disease.肾移植患者中乙肝病毒核心基因缺失突变体的积累和持续存在与终末期肝病相关。
Hepatology. 1996 Oct;24(4):751-8. doi: 10.1002/hep.510240401.
9
A host factor that binds near the termini of hepatitis B virus pregenomic RNA.一种结合在乙型肝炎病毒前基因组RNA末端附近的宿主因子。
J Virol. 1996 Oct;70(10):6803-9. doi: 10.1128/JVI.70.10.6803-6809.1996.
10
Effects of a naturally occurring mutation in the hepatitis B virus basal core promoter on precore gene expression and viral replication.乙肝病毒核心启动子自然发生的突变对前核心基因表达及病毒复制的影响
J Virol. 1996 Sep;70(9):5845-51. doi: 10.1128/JVI.70.9.5845-5851.1996.

含核心区内部缺失突变的人乙型肝炎病毒自然发生变异体的功能特性分析

Functional characterization of naturally occurring variants of human hepatitis B virus containing the core internal deletion mutation.

作者信息

Yuan T T, Lin M H, Qiu S M, Shih C

机构信息

Department of Pathology, Center for Tropical Diseases, University of Texas Medical Branch, Galveston 77555-0609, USA.

出版信息

J Virol. 1998 Mar;72(3):2168-76. doi: 10.1128/JVI.72.3.2168-2176.1998.

DOI:10.1128/JVI.72.3.2168-2176.1998
PMID:9499073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109512/
Abstract

Naturally occurring variants of human hepatitis B virus (HBV) containing the core internal deletion (CID) mutation have been found frequently in HBV carriers worldwide. Despite numerous sequence analysis reports of CID variants in patients, in the past decade, CID variants have not been characterized functionally, and thus their biological significance to HBV infection remains unclear. We report here two different CID variants identified from two patients that are replication defective, most likely due to the absence of detectable core protein. In addition, we were unable to detect the presence of the precore protein and e antigen from CID variants. However, the production of polymerase appeared to be normal. The replication defect of the CID variants can be rescued in trans by complementation with wild-type core protein. The rescued CID variant particles, which utilize the wild-type core protein, presumably are enveloped properly since they can be secreted into the medium and band at a position similar to that of mature wild-type Dane particles, as determined by gradient centrifugation analysis. Our results also provide an explanation for the association of CID variants with helper or wild-type HBV in nature. The significance of CID variants in HBV infection and pathogenesis is discussed.

摘要

在全球乙肝病毒(HBV)携带者中,经常发现含有核心内部缺失(CID)突变的人类乙肝病毒自然发生变体。尽管有大量关于患者中CID变体的序列分析报告,但在过去十年中,CID变体尚未进行功能表征,因此它们对HBV感染的生物学意义仍不清楚。我们在此报告从两名患者中鉴定出的两种不同的CID变体,它们复制缺陷,最可能是由于未检测到核心蛋白。此外,我们无法检测到CID变体中前核心蛋白和e抗原的存在。然而,聚合酶的产生似乎正常。CID变体的复制缺陷可通过与野生型核心蛋白互补在反式中得到挽救。利用野生型核心蛋白的挽救后的CID变体颗粒,推测由于它们可分泌到培养基中并在类似于成熟野生型丹氏颗粒的位置出现条带(通过梯度离心分析确定),因此被正确包膜。我们的结果也为CID变体在自然界中与辅助性或野生型HBV相关联提供了解释。讨论了CID变体在HBV感染和发病机制中的意义。