• 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

乙型肝炎病毒X基因在哺乳动物细胞中的表达。

Expression of the hepatitis B virus X gene in mammalian cells.

作者信息

Siddiqui A, Jameel S, Mapoles J

出版信息

Proc Natl Acad Sci U S A. 1987 Apr;84(8):2513-7. doi: 10.1073/pnas.84.8.2513.

DOI:10.1073/pnas.84.8.2513
PMID:3494252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC304684/
Abstract

The hepatitis B virus (HBV) DNA contains an open reading frame (ORF) designated X, which has the capacity to encode a protein of 16,560 Da (subtype adw). Such a protein has not been identified in either HBV particles or infected human livers, and therefore its role in the viral life cycle remains unknown. We report here the expression of the HBV X ORF in cultured cells using recombinant vectors. A protein of 16 kDa was identified by means of an antiserum prepared against a synthetic peptide and with human antisera from hepatitis B patients as well as those with hepatocellular carcinoma. Cell fractionation and immunofluorescence studies suggest a probable association with cytoskeletal components. Our studies further located a promoter sequence upstream of the X ORF, which directs the transcription of a 0.7- to 0.8-kilobase X-specific RNA in transfected human hepatoma cells.

摘要

乙肝病毒(HBV)DNA包含一个名为X的开放阅读框(ORF),它能够编码一种16,560道尔顿的蛋白质(adw亚型)。在HBV颗粒或受感染的人类肝脏中均未鉴定出这种蛋白质,因此其在病毒生命周期中的作用仍然未知。我们在此报告使用重组载体在培养细胞中表达HBV X ORF的情况。通过针对合成肽制备的抗血清以及来自乙肝患者和肝癌患者的人抗血清鉴定出了一种16 kDa的蛋白质。细胞分级分离和免疫荧光研究表明其可能与细胞骨架成分有关。我们的研究进一步确定了X ORF上游的一个启动子序列,该序列在转染的人肝癌细胞中指导0.7至0.8千碱基X特异性RNA的转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/18a5c09ad1f0/pnas00273-0415-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/17d529ea7524/pnas00273-0413-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/5cb2a041288b/pnas00273-0413-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/a6c349bedfaa/pnas00273-0413-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/b46f00914493/pnas00273-0414-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/eaaff1930b62/pnas00273-0414-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/a2b0392f3017/pnas00273-0414-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/18a5c09ad1f0/pnas00273-0415-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/17d529ea7524/pnas00273-0413-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/5cb2a041288b/pnas00273-0413-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/a6c349bedfaa/pnas00273-0413-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/b46f00914493/pnas00273-0414-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/eaaff1930b62/pnas00273-0414-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/a2b0392f3017/pnas00273-0414-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08af/304684/18a5c09ad1f0/pnas00273-0415-a.jpg

相似文献

1
Expression of the hepatitis B virus X gene in mammalian cells.乙型肝炎病毒X基因在哺乳动物细胞中的表达。
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2513-7. doi: 10.1073/pnas.84.8.2513.
2
Identification of a promoter element located upstream from the hepatitis B virus X gene.对位于乙型肝炎病毒X基因上游的启动子元件的鉴定。
Mol Cell Biol. 1987 Jan;7(1):545-8. doi: 10.1128/mcb.7.1.545-548.1987.
3
trans-activation of viral enhancers by the hepatitis B virus X protein.乙型肝炎病毒X蛋白对病毒增强子的反式激活作用。
J Virol. 1988 Feb;62(2):427-34. doi: 10.1128/JVI.62.2.427-434.1988.
4
The enhancer sequence of human hepatitis B virus can enhance the activity of its surface gene promoter.人类乙型肝炎病毒的增强子序列可增强其表面基因启动子的活性。
Nucleic Acids Res. 1987 Mar 11;15(5):2261-8. doi: 10.1093/nar/15.5.2261.
5
The HBV X-ORF encodes a transactivator: a potential factor in viral hepatocarcinogenesis.乙肝病毒X开放阅读框编码一种反式激活因子:病毒诱发肝癌的一个潜在因素。
Oncogene. 1988 Aug;3(2):169-77.
6
A liver-specific enhancer in the core promoter region of human hepatitis B virus.人类乙型肝炎病毒核心启动子区域中的肝脏特异性增强子。
Science. 1989 Nov 3;246(4930):658-61. doi: 10.1126/science.2554495.
7
Identification of hepatitis B virus polypeptides encoded by the entire pre-s open reading frame.对整个前S开放阅读框编码的乙型肝炎病毒多肽的鉴定。
J Virol. 1985 Jul;55(1):223-31. doi: 10.1128/JVI.55.1.223-231.1985.
8
Hepatitis B virus X gene can transactivate heterologous viral sequences.乙型肝炎病毒X基因可反式激活异源病毒序列。
Proc Natl Acad Sci U S A. 1989 Mar;86(6):2046-50. doi: 10.1073/pnas.86.6.2046.
9
Hepatitis B virus (HBV) X gene expression in human cells and anti-HBx antibodies detection in chronic HBV infection.人细胞中乙型肝炎病毒(HBV)X基因表达及慢性HBV感染中抗HBx抗体检测
Virology. 1990 Jan;174(1):299-304. doi: 10.1016/0042-6822(90)90079-7.
10
A transcription initiation site for the hepatitis B virus X gene is directed by the promoter-binding protein.乙肝病毒X基因的转录起始位点由启动子结合蛋白引导。
J Virol. 1993 May;67(5):2559-65. doi: 10.1128/JVI.67.5.2559-2565.1993.

引用本文的文献

1
Integrated hepatitis B virus DNA maintains surface antigen production during antiviral treatment.整合的乙型肝炎病毒 DNA 在抗病毒治疗期间维持表面抗原的产生。
J Clin Invest. 2022 Sep 15;132(18). doi: 10.1172/JCI161818.
2
Modulation of hepatitis B virus pregenomic RNA stability and splicing by histone deacetylase 5 enhances viral biosynthesis.组蛋白去乙酰化酶 5 调节乙型肝炎病毒前基因组 RNA 的稳定性和剪接,增强病毒生物合成。
PLoS Pathog. 2020 Aug 21;16(8):e1008802. doi: 10.1371/journal.ppat.1008802. eCollection 2020 Aug.
3
Revisiting Hepatitis B Virus: Challenges of Curative Therapies.

本文引用的文献

1
Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells.在哺乳动物细胞中表达氯霉素乙酰转移酶的重组基因组。
Mol Cell Biol. 1982 Sep;2(9):1044-51. doi: 10.1128/mcb.2.9.1044-1051.1982.
2
Core and E antigen synthesis in rodent cells transformed with hepatitis B virus DNA is associated with greater than genome length viral messenger RNAs.用乙肝病毒DNA转化的啮齿动物细胞中核心抗原和E抗原的合成与大于基因组长度的病毒信使核糖核酸有关。
J Mol Biol. 1983 Apr 25;165(4):683-99. doi: 10.1016/s0022-2836(83)80274-5.
3
Cell-specific expression controlled by the 5'-flanking region of insulin and chymotrypsin genes.
重新审视乙型肝炎病毒:治愈疗法的挑战。
J Virol. 2019 Sep 30;93(20). doi: 10.1128/JVI.01032-19. Print 2019 Oct 15.
4
Correlations between mitochondrial DNA haplogroup D5 and chronic hepatitis B virus infection in Yunnan, China.线粒体 DNA 单倍群 D5 与中国云南地区慢性乙型肝炎病毒感染的相关性。
Sci Rep. 2018 Jan 17;8(1):869. doi: 10.1038/s41598-018-19184-6.
5
The Molecular and Structural Basis of HBV-resistance to Nucleos(t)ide Analogs.HBV 耐药的分子和结构基础。
J Clin Transl Hepatol. 2014 Sep;2(3):202-11. doi: 10.14218/JCTH.2014.00021. Epub 2014 Sep 15.
6
Hepatitis B virus disrupts mitochondrial dynamics: induces fission and mitophagy to attenuate apoptosis.乙型肝炎病毒破坏线粒体动力学:诱导分裂和线粒体自噬以减轻细胞凋亡。
PLoS Pathog. 2013;9(12):e1003722. doi: 10.1371/journal.ppat.1003722. Epub 2013 Dec 5.
7
The new core promoter element XCPE1 (X Core Promoter Element 1) directs activator-, mediator-, and TATA-binding protein-dependent but TFIID-independent RNA polymerase II transcription from TATA-less promoters.新型核心启动子元件XCPE1(X核心启动子元件1)指导无TATA盒启动子进行依赖激活因子、中介体和TATA结合蛋白,但不依赖TFIID的RNA聚合酶II转录。
Mol Cell Biol. 2007 Mar;27(5):1844-58. doi: 10.1128/MCB.01363-06. Epub 2007 Jan 8.
8
Novel type of hepatitis B virus mutation: replacement mutation involving a hepatocyte nuclear factor 1 binding site tandem repeat in chronic hepatitis B virus genotype E.新型乙型肝炎病毒突变:慢性乙型肝炎病毒E基因型中涉及肝细胞核因子1结合位点串联重复的置换突变。
J Virol. 2005 Nov;79(22):14404-10. doi: 10.1128/JVI.79.22.14404-14410.2005.
9
The enigmatic X gene of hepatitis B virus.乙型肝炎病毒神秘的X基因。
J Virol. 2004 Dec;78(23):12725-34. doi: 10.1128/JVI.78.23.12725-12734.2004.
10
Nuclear respiratory factor 1 plays an essential role in transcriptional initiation from the hepatitis B virus x gene promoter.核呼吸因子1在乙肝病毒X基因启动子的转录起始过程中发挥着至关重要的作用。
J Virol. 2004 Oct;78(20):10856-64. doi: 10.1128/JVI.78.20.10856-10864.2004.
由胰岛素基因和胰凝乳蛋白酶基因的5'侧翼区域控制的细胞特异性表达。
Nature. 1983;306(5943):557-61. doi: 10.1038/306557a0.
4
Analysis of processing and polyadenylation signals of the hepatitis B virus surface antigen gene by using simian virus 40-hepatitis B virus chimeric plasmids.利用猴病毒40-乙型肝炎病毒嵌合质粒分析乙型肝炎病毒表面抗原基因的加工和聚腺苷酸化信号
Mol Cell Biol. 1983 Dec;3(12):2250-8. doi: 10.1128/mcb.3.12.2250-2258.1983.
5
High efficiency polyoma DNA transfection of chloroquine treated cells.氯喹处理细胞的高效多瘤病毒DNA转染
Nucleic Acids Res. 1983 Mar 11;11(5):1295-308. doi: 10.1093/nar/11.5.1295.
6
Expression of hepatitis B virus surface antigen gene in cultured cells by using recombinant plasmid vectors.利用重组质粒载体在培养细胞中表达乙型肝炎病毒表面抗原基因。
Mol Cell Biol. 1983 Jan;3(1):143-6. doi: 10.1128/mcb.3.1.143-146.1983.
7
The Rous sarcoma virus long terminal repeat is a strong promoter when introduced into a variety of eukaryotic cells by DNA-mediated transfection.劳氏肉瘤病毒长末端重复序列通过DNA介导转染导入多种真核细胞时是一个强启动子。
Proc Natl Acad Sci U S A. 1982 Nov;79(22):6777-81. doi: 10.1073/pnas.79.22.6777.
8
SV40-transformed simian cells support the replication of early SV40 mutants.猴空泡病毒 40(SV40)转化的猿猴细胞支持早期 SV40 突变体的复制。
Cell. 1981 Jan;23(1):175-82. doi: 10.1016/0092-8674(81)90282-8.
9
Human hepatocellular carcinoma cell lines secrete the major plasma proteins and hepatitis B surface antigen.人肝癌细胞系分泌主要血浆蛋白和乙型肝炎表面抗原。
Science. 1980 Jul 25;209(4455):497-9. doi: 10.1126/science.6248960.
10
Transcription of the hepatitis B surface antigen gene in cultured murine cells initiates within the presurface region.乙型肝炎表面抗原基因在培养的鼠细胞中的转录起始于前表面区域内。
J Virol. 1984 May;50(2):563-71. doi: 10.1128/JVI.50.2.563-571.1984.