• 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

在爱泼斯坦-巴尔病毒感染的潜伏和裂解阶段,来自C/W、F和Q启动子的EBNA1基因转录本在爱泼斯坦-巴尔病毒转化的淋巴样细胞中的相对水平。

Relative levels of EBNA1 gene transcripts from the C/W, F and Q promoters in Epstein-Barr virus-transformed lymphoid cells in latent and lytic stages of infection.

作者信息

Zetterberg H, Stenglein M, Jansson A, Ricksten A, Rymo L

出版信息

J Gen Virol. 1999 Feb;80 ( Pt 2):457-466. doi: 10.1099/0022-1317-80-2-457.

DOI:10.1099/0022-1317-80-2-457
PMID:10073708
Abstract

Four promoters, Cp, Wp, Fp and Qp, are known to participate in transcription of the Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA1) gene in EBV-infected cell lines. The promoters are used differentially during the different phases of infection and establishment of the stages of latency. This has raised questions about the regulation of the promoters and the molecular mechanisms underlying the switches between them. To obtain a measure of the activity of the different EBNA1 transcription units in EBV-transformed cell lines of different phenotypes, RNA probes were constructed that allowed the detection and relative quantification, by RNase protection analysis, of EBNA1 transcripts initiated at Fp and Qp and, in an indirect manner, Cp/Wp. RNase protection and PCR assays were performed with cytoplasmic RNA from B-lymphoid cell lines in latency stages I, II-III and III and after induction of the virus lytic cycle. The experiments demonstrated that, in addition to previously identified EBNA1 transcripts, cell lines of all latency types also contained different mRNAs that carried sequences from the EBNA1-encoding K exon. Induction of the virus lytic cycle resulted in low levels of an FpQ/U/K-spliced transcript. However, there was a large increase of FpQ- and FpQ/U-spliced transcripts with unknown 3' sequences. Furthermore, a new transcript, initiated at an unidentified site 5' of the BamHI f/K cleavage site and continuing through BamHI K into the EBNA1-encoding K exon without interruption, was produced in substantial amounts in the lytic cycle.

摘要

已知有四个启动子,即Cp、Wp、Fp和Qp,参与了爱泼斯坦-巴尔病毒(EBV)感染细胞系中EBV核抗原1(EBNA1)基因的转录。在感染的不同阶段以及潜伏期各阶段的建立过程中,这些启动子的使用存在差异。这引发了关于启动子调控以及它们之间转换的分子机制的问题。为了衡量不同表型的EBV转化细胞系中不同EBNA1转录单元的活性,构建了RNA探针,通过核糖核酸酶保护分析,能够检测并相对定量从Fp和Qp起始的EBNA1转录本,以及以间接方式检测从Cp/Wp起始的转录本。对处于潜伏期I、II - III和III阶段以及病毒裂解周期诱导后的B淋巴细胞系的细胞质RNA进行了核糖核酸酶保护和PCR检测。实验表明,除了先前鉴定出的EBNA1转录本外,所有潜伏期类型的细胞系还含有不同的mRNA,这些mRNA携带了来自编码EBNA1的K外显子的序列。病毒裂解周期的诱导导致了低水平的FpQ/U/K剪接转录本。然而,具有未知3'序列的FpQ和FpQ/U剪接转录本大幅增加。此外,在裂解周期中大量产生了一种新的转录本,它从BamHI f/K切割位点5'端的一个未确定位点起始,不间断地穿过BamHI K进入编码EBNA1的K外显子。

相似文献

1
Relative levels of EBNA1 gene transcripts from the C/W, F and Q promoters in Epstein-Barr virus-transformed lymphoid cells in latent and lytic stages of infection.在爱泼斯坦-巴尔病毒感染的潜伏和裂解阶段,来自C/W、F和Q启动子的EBNA1基因转录本在爱泼斯坦-巴尔病毒转化的淋巴样细胞中的相对水平。
J Gen Virol. 1999 Feb;80 ( Pt 2):457-466. doi: 10.1099/0022-1317-80-2-457.
2
The Epstein-Barr virus (EBV) nuclear antigen 1 BamHI F promoter is activated on entry of EBV-transformed B cells into the lytic cycle.爱泼斯坦-巴尔病毒(EBV)核抗原1 BamHI F启动子在EBV转化的B细胞进入裂解周期时被激活。
J Virol. 1992 Dec;66(12):7461-8. doi: 10.1128/JVI.66.12.7461-7468.1992.
3
A simple reverse transcriptase PCR assay to distinguish EBNA1 gene transcripts associated with type I and II latency from those arising during induction of the viral lytic cycle.一种简单的逆转录酶聚合酶链反应检测方法,用于区分与I型和II型潜伏相关的EBNA1基因转录本与病毒裂解周期诱导过程中产生的转录本。
J Virol. 1996 Nov;70(11):8204-8. doi: 10.1128/JVI.70.11.8204-8208.1996.
4
Epstein-Barr virus latency in blood mononuclear cells: analysis of viral gene transcription during primary infection and in the carrier state.爱泼斯坦-巴尔病毒在血液单核细胞中的潜伏:原发性感染及携带状态下病毒基因转录分析
J Virol. 1994 Nov;68(11):7374-85. doi: 10.1128/JVI.68.11.7374-7385.1994.
5
Transcription of the Epstein-Barr virus nuclear antigen 1 (EBNA1) gene occurs before induction of the BCR2 (Cp) EBNA gene promoter during the initial stages of infection in B cells.在B细胞感染的初始阶段,爱泼斯坦-巴尔病毒核抗原1(EBNA1)基因的转录发生在BCR2(Cp)EBNA基因启动子诱导之前。
J Virol. 1996 Jun;70(6):3561-70. doi: 10.1128/JVI.70.6.3561-3570.1996.
6
Activity of the EBNA1 promoter associated with lytic replication (Fp) in Epstein-Barr virus associated disorders.与爱泼斯坦-巴尔病毒相关疾病中裂解性复制相关的EBNA1启动子(Fp)的活性
Mol Pathol. 2001 Apr;54(2):98-102. doi: 10.1136/mp.54.2.98.
7
Latency pattern of Epstein-Barr virus and methylation status in Epstein-Barr virus-associated hemophagocytic syndrome.爱泼斯坦-巴尔病毒潜伏期模式及爱泼斯坦-巴尔病毒相关噬血细胞综合征中的甲基化状态
J Med Virol. 2003 Jul;70(3):410-9. doi: 10.1002/jmv.10411.
8
Dual EBNA1 promoter usage by Epstein-Barr virus in human B-cell lines expressing unique intermediate cellular phenotypes.爱泼斯坦-巴尔病毒在表达独特中间细胞表型的人B细胞系中对EBNA1双启动子的使用情况
J Virol. 1994 Oct;68(10):6421-31. doi: 10.1128/JVI.68.10.6421-6431.1994.
9
Methylation of the EBV genome and establishment of restricted latency in low-passage EBV-infected 293 epithelial cells.EBV基因组的甲基化以及低传代EBV感染的293上皮细胞中受限潜伏期的建立。
Virology. 2002 Jul 20;299(1):109-21. doi: 10.1006/viro.2002.1457.
10
Heat shock factor 1 upregulates transcription of Epstein-Barr Virus nuclear antigen 1 by binding to a heat shock element within the BamHI-Q promoter.热休克因子 1 通过与 BamHI-Q 启动子内的热休克元件结合,上调 Epstein-Barr 病毒核抗原 1 的转录。
Virology. 2011 Dec 20;421(2):184-91. doi: 10.1016/j.virol.2011.10.001. Epub 2011 Oct 21.

引用本文的文献

1
Epigenetic Mechanisms in Latent Epstein-Barr Virus Infection and Associated Cancers.潜伏性EB病毒感染及相关癌症中的表观遗传机制
Cancers (Basel). 2024 Feb 29;16(5):991. doi: 10.3390/cancers16050991.
2
Methylation status and AP1 elements are involved in EBV-mediated miR-155 expression in EBV positive lymphoma cells.甲基化状态和活化蛋白1元件参与EB病毒阳性淋巴瘤细胞中EB病毒介导的miR-155表达。
Virology. 2016 Jul;494:158-67. doi: 10.1016/j.virol.2016.04.005. Epub 2016 Apr 26.
3
EBV infection is common in gingival epithelial cells of the periodontium and worsens during chronic periodontitis.
EBV 感染在牙周组织的牙龈上皮细胞中很常见,并且在慢性牙周炎期间恶化。
PLoS One. 2013 Dec 19;8(12):e80336. doi: 10.1371/journal.pone.0080336. eCollection 2013.
4
Functions of the Epstein-Barr virus EBNA1 protein in viral reactivation and lytic infection.EB 病毒 EBNA1 蛋白在病毒再激活和裂解感染中的功能。
J Virol. 2012 Jun;86(11):6146-58. doi: 10.1128/JVI.00013-12. Epub 2012 Apr 4.
5
Epithelial cell retention of transcriptionally active, P3HR-1-derived heterogeneous Epstein-Barr virus DNA with concurrent loss of parental virus.上皮细胞中保留转录活跃、源自 P3HR-1 的异质性 Epstein-Barr 病毒 DNA,同时丧失亲代病毒。
J Virol. 2011 Aug;85(15):7634-43. doi: 10.1128/JVI.00045-11. Epub 2011 May 18.
6
The p38 signaling pathway upregulates expression of the Epstein-Barr virus LMP1 oncogene.p38 信号通路上调 Epstein-Barr 病毒 LMP1 癌基因的表达。
J Virol. 2010 Mar;84(6):2787-97. doi: 10.1128/JVI.01052-09. Epub 2010 Jan 6.
7
Epstein-Barr virus latency switch in human B-cells: a physico-chemical model.人类B细胞中爱泼斯坦-巴尔病毒潜伏期转换:一个物理化学模型
BMC Syst Biol. 2007 Aug 31;1:40. doi: 10.1186/1752-0509-1-40.
8
Epstein-Barr virus mRNA export factor EB2 is essential for production of infectious virus.爱泼斯坦-巴尔病毒mRNA输出因子EB2对传染性病毒的产生至关重要。
J Virol. 2002 Oct;76(19):9635-44. doi: 10.1128/jvi.76.19.9635-9644.2002.
9
Epstein-Barr virus nuclear antigen 5 inhibits pre-mRNA cleavage and polyadenylation.爱泼斯坦-巴尔病毒核抗原5抑制前体mRNA的切割和多聚腺苷酸化。
Nucleic Acids Res. 2002 May 15;30(10):2131-43. doi: 10.1093/nar/30.10.2131.
10
Promoter-proximal regulatory elements involved in oriP-EBNA1-independent and -dependent activation of the Epstein-Barr virus C promoter in B-lymphoid cell lines.参与B淋巴细胞系中爱泼斯坦-巴尔病毒C启动子的oriP-EBNA1非依赖性和依赖性激活的启动子近端调控元件。
J Virol. 2001 Jul;75(13):5796-811. doi: 10.1128/JVI.75.13.5796-5811.2001.