• 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
Inhibition of the FACT Complex Reduces Transcription from the Human Cytomegalovirus Major Immediate Early Promoter in Models of Lytic and Latent Replication.在裂解性和潜伏性复制模型中,抑制FACT复合物可降低人巨细胞病毒主要立即早期启动子的转录。
J Virol. 2016 Mar 28;90(8):4249-4253. doi: 10.1128/JVI.02501-15. Print 2016 Apr.
2
Human cytomegalovirus major immediate early transcripts arise predominantly from the canonical major immediate early promoter in reactivating progenitor-derived dendritic cells.人巨细胞病毒主要早期转录物主要来源于激活前体细胞来源的树突状细胞中的经典主要早期启动子。
J Gen Virol. 2020 Jun;101(6):635-644. doi: 10.1099/jgv.0.001419.
3
Chromatin structure regulates human cytomegalovirus gene expression during latency, reactivation and lytic infection.染色质结构在潜伏、再激活和裂解感染期间调节人巨细胞病毒基因表达。
Biochim Biophys Acta. 2010 Mar-Apr;1799(3-4):286-95. doi: 10.1016/j.bbagrm.2009.08.001. Epub 2009 Aug 12.
4
Human cytomegalovirus G protein-coupled receptor US28 promotes latency by attenuating c-fos.人巨细胞病毒 G 蛋白偶联受体 US28 通过衰减 c-fos 促进潜伏。
Proc Natl Acad Sci U S A. 2019 Jan 29;116(5):1755-1764. doi: 10.1073/pnas.1816933116. Epub 2019 Jan 15.
5
The Elk-1 and serum response factor binding sites in the major immediate-early promoter of human cytomegalovirus are required for efficient viral replication in quiescent cells and compensate for inactivation of the NF-kappaB sites in proliferating cells.人巨细胞病毒主要即刻早期启动子中的 Elk-1 和血清反应因子结合位点对于静止细胞中的病毒复制效率是必需的,并补偿了增殖细胞中 NF-κB 位点的失活。
J Virol. 2010 May;84(9):4481-93. doi: 10.1128/JVI.02141-09. Epub 2010 Feb 10.
6
Control of cytomegalovirus lytic gene expression by histone acetylation.通过组蛋白乙酰化控制巨细胞病毒裂解基因表达
EMBO J. 2002 Mar 1;21(5):1112-20. doi: 10.1093/emboj/21.5.1112.
7
Alternative promoters drive human cytomegalovirus reactivation from latency.替代启动子驱动人类巨细胞病毒从潜伏中重新激活。
Proc Natl Acad Sci U S A. 2019 Aug 27;116(35):17492-17497. doi: 10.1073/pnas.1900783116. Epub 2019 Aug 13.
8
FOXO transcription factors activate alternative major immediate early promoters to induce human cytomegalovirus reactivation.FOXO 转录因子激活替代的主要即刻早期启动子,诱导人巨细胞病毒激活。
Proc Natl Acad Sci U S A. 2020 Aug 4;117(31):18764-18770. doi: 10.1073/pnas.2002651117. Epub 2020 Jul 21.
9
Regulation of host and viral promoters during human cytomegalovirus latency via US28 and CTCF.通过 US28 和 CTCF 调控人巨细胞病毒潜伏时的宿主和病毒启动子。
J Gen Virol. 2021 May;102(5). doi: 10.1099/jgv.0.001609.
10
Repression of the major immediate early promoter of human cytomegalovirus allows transcription from an alternate promoter.人巨细胞病毒主要早期启动子的抑制允许从替代启动子转录。
J Gen Virol. 2023 Sep;104(9). doi: 10.1099/jgv.0.001894.

引用本文的文献

1
Inhibition of MAPK signaling suppresses cytomegalovirus reactivation in CD34 Kasumi-3 cells.丝裂原活化蛋白激酶(MAPK)信号通路的抑制可抑制CD34 Kasumi-3细胞中巨细胞病毒的重新激活。
bioRxiv. 2025 Feb 13:2025.02.13.638080. doi: 10.1101/2025.02.13.638080.
2
Impact of the interaction between herpes simplex virus 1 ICP22 and FACT on viral gene expression and pathogenesis.单纯疱疹病毒 1 ICP22 与 FACT 之间的相互作用对病毒基因表达和发病机制的影响。
J Virol. 2024 Aug 20;98(8):e0073724. doi: 10.1128/jvi.00737-24. Epub 2024 Jul 17.
3
Primal FEAR protects against infection.原始恐惧可预防感染。
Nat Microbiol. 2024 Apr;9(4):886-888. doi: 10.1038/s41564-024-01649-2.
4
Critical Role for the Human Cytomegalovirus Major Immediate Early Proteins in Recruitment of RNA Polymerase II and H3K27Ac To an Enhancer-Like Element in Ori.人巨细胞病毒主要早期蛋白在 RNA 聚合酶 II 和 H3K27Ac 募集到 Ori 的增强子样元件中的关键作用。
Microbiol Spectr. 2023 Feb 14;11(1):e0314422. doi: 10.1128/spectrum.03144-22. Epub 2023 Jan 16.
5
Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins.细小病毒非结构蛋白 2 与染色质调节细胞蛋白相互作用。
PLoS Pathog. 2022 Apr 8;18(4):e1010353. doi: 10.1371/journal.ppat.1010353. eCollection 2022 Apr.
6
Modulation of host cell signaling during cytomegalovirus latency and reactivation.巨细胞病毒潜伏和再激活期间宿主细胞信号的调节。
Virol J. 2021 Oct 18;18(1):207. doi: 10.1186/s12985-021-01674-1.
7
Histone Deacetylase Inhibitor SAHA Induces Expression of Fatty Acid-Binding Protein 4 and Inhibits Replication of Human Cytomegalovirus.组蛋白去乙酰化酶抑制剂 SAHA 诱导脂肪酸结合蛋白 4 的表达并抑制人巨细胞病毒的复制。
Virol Sin. 2021 Dec;36(6):1352-1362. doi: 10.1007/s12250-021-00382-y. Epub 2021 Jun 22.
8
Epigenetic reprogramming of host and viral genes by Human Cytomegalovirus infection in Kasumi-3 myeloid progenitor cells at early times post-infection.人巨细胞病毒感染后早期,Kasumi-3髓系祖细胞中宿主和病毒基因的表观遗传重编程。
J Virol. 2021 May 10;95(11). doi: 10.1128/JVI.00183-21. Epub 2021 Mar 17.
9
Regulation of the MIE Locus During HCMV Latency and Reactivation.人巨细胞病毒潜伏和再激活过程中主要立即早期基因座的调控
Pathogens. 2020 Oct 23;9(11):869. doi: 10.3390/pathogens9110869.
10
Control of Immediate Early Gene Expression for Human Cytomegalovirus Reactivation.人巨细胞病毒激活即刻早期基因表达的控制。
Front Cell Infect Microbiol. 2020 Sep 17;10:476. doi: 10.3389/fcimb.2020.00476. eCollection 2020.

本文引用的文献

1
Hematopoietic long-term culture (hLTC) for human cytomegalovirus latency and reactivation.用于人类巨细胞病毒潜伏和再激活的造血长期培养(hLTC)
Methods Mol Biol. 2014;1119:99-112. doi: 10.1007/978-1-62703-788-4_7.
2
Human cytomegalovirus pUL78 G protein-coupled receptor homologue is required for timely cell entry in epithelial cells but not fibroblasts.人类巨细胞病毒 pUL78 G 蛋白偶联受体同源物是上皮细胞而不是成纤维细胞中及时进入细胞所必需的。
J Virol. 2012 Nov;86(21):11425-33. doi: 10.1128/JVI.05900-11. Epub 2012 Aug 22.
3
A myeloid progenitor cell line capable of supporting human cytomegalovirus latency and reactivation, resulting in infectious progeny.能够支持人类巨细胞病毒潜伏和激活并产生感染性后代的髓系祖细胞系。
J Virol. 2012 Sep;86(18):9854-65. doi: 10.1128/JVI.01278-12. Epub 2012 Jul 3.
4
Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells.FACT在哺乳动物组织中的表达表明其在维持细胞未分化状态中发挥作用。
Oncotarget. 2011 Oct;2(10):783-96. doi: 10.18632/oncotarget.340.
5
Curaxins: anticancer compounds that simultaneously suppress NF-κB and activate p53 by targeting FACT.Curaxins:通过靶向 FACT 同时抑制 NF-κB 并激活 p53 的抗癌化合物。
Sci Transl Med. 2011 Aug 10;3(95):95ra74. doi: 10.1126/scitranslmed.3002530.
6
TNFR1-induced activation of the classical NF-κB pathway.肿瘤坏死因子受体 1 诱导的经典 NF-κB 通路的激活。
FEBS J. 2011 Apr;278(6):862-76. doi: 10.1111/j.1742-4658.2011.08015.x. Epub 2011 Feb 8.
7
Analysis of latent viral gene expression in natural and experimental latency models of human cytomegalovirus and its correlation with histone modifications at a latent promoter.人巨细胞病毒天然和实验潜伏模型中潜伏病毒基因表达的分析及其与潜伏启动子处组蛋白修饰的相关性。
J Gen Virol. 2010 Mar;91(Pt 3):599-604. doi: 10.1099/vir.0.015602-0. Epub 2009 Nov 11.
8
Dynamic histone H3 acetylation and methylation at human cytomegalovirus promoters during replication in fibroblasts.人巨细胞病毒在成纤维细胞中复制期间其启动子处的动态组蛋白H3乙酰化和甲基化
J Virol. 2008 Oct;82(19):9525-36. doi: 10.1128/JVI.00946-08. Epub 2008 Jul 23.
9
Human cytomegalovirus gene expression is silenced by Daxx-mediated intrinsic immune defense in model latent infections established in vitro.在体外建立的模型潜伏感染中,人巨细胞病毒基因表达通过Daxx介导的固有免疫防御而沉默。
J Virol. 2007 Sep;81(17):9109-20. doi: 10.1128/JVI.00827-07. Epub 2007 Jun 27.
10
The interleukin 1beta-induced expression of human prostaglandin F2alpha receptor messenger RNA in human myometrial-derived ULTR cells requires the transcription factor, NFkappaB.白细胞介素1β诱导人子宫肌层来源的ULTR细胞中前列腺素F2α受体信使核糖核酸的表达需要转录因子核因子κB。
Biol Reprod. 2006 Nov;75(5):697-704. doi: 10.1095/biolreprod.106.053439. Epub 2006 Jul 19.

在裂解性和潜伏性复制模型中,抑制FACT复合物可降低人巨细胞病毒主要立即早期启动子的转录。

Inhibition of the FACT Complex Reduces Transcription from the Human Cytomegalovirus Major Immediate Early Promoter in Models of Lytic and Latent Replication.

作者信息

O'Connor Christine M, Nukui Masatoshi, Gurova Katerina V, Murphy Eain A

机构信息

Department of Microbiology and Immunology, University at Buffalo-SUNY, Buffalo, New York, USA.

FORGE Life Science, LLC, Baruch S. Blumberg Research Institute, Doylestown, Pennsylvania, USA.

出版信息

J Virol. 2016 Mar 28;90(8):4249-4253. doi: 10.1128/JVI.02501-15. Print 2016 Apr.

DOI:10.1128/JVI.02501-15
PMID:26865717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4810550/
Abstract

The successful colonization of the majority of the population by human cytomegalovirus is a direct result of the virus's ability to establish and, more specifically, reactivate from latency. The underlying cellular factors involved in viral reactivation remain unknown. Here, we show that the host complexfacilitateschromatintranscription (FACT) binds to the major immediate early promoter (MIEP) and that inhibition of this complex reduces MIEP transactivation, thus inhibiting viral reactivation.

摘要

人巨细胞病毒在大多数人群中的成功定植是该病毒建立潜伏并更具体地从潜伏状态重新激活能力的直接结果。参与病毒重新激活的潜在细胞因子仍然未知。在这里,我们表明宿主促进染色质转录(FACT)复合物与主要立即早期启动子(MIEP)结合,并且对该复合物的抑制会降低MIEP的反式激活,从而抑制病毒重新激活。