• 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

腺病毒晚期基因表达不需要类似Rev的核RNA输出途径。

Adenovirus late gene expression does not require a Rev-like nuclear RNA export pathway.

作者信息

Rabino C, Aspegren A, Corbin-Lickfett K, Bridge E

机构信息

Rudbeck Laboratory, Department of Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.

出版信息

J Virol. 2000 Jul;74(14):6684-8. doi: 10.1128/jvi.74.14.6684-6688.2000.

DOI:10.1128/jvi.74.14.6684-6688.2000
PMID:10864686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC112182/
Abstract

Adenovirus late mRNA export is facilitated by viral early proteins of 55 and 34 kDa. The 34-kDa protein contains a leucine-rich nuclear export signal (NES) similar to that of the human immunodeficiency virus Rev protein. It was proposed that the 34-kDa protein might facilitate the export of adenovirus late mRNA through a Rev-like NES-mediated export pathway. We have tested the role of NES-mediated RNA export during adenovirus infection, and we find that it is not essential for the expression of adenovirus late genes.

摘要

腺病毒晚期mRNA的输出由55 kDa和34 kDa的病毒早期蛋白促进。34 kDa的蛋白含有一个富含亮氨酸的核输出信号(NES),类似于人类免疫缺陷病毒Rev蛋白的核输出信号。有人提出,34 kDa的蛋白可能通过类似Rev的NES介导的输出途径促进腺病毒晚期mRNA的输出。我们测试了NES介导的RNA输出在腺病毒感染过程中的作用,发现它对于腺病毒晚期基因的表达并非必不可少。

相似文献

1
Adenovirus late gene expression does not require a Rev-like nuclear RNA export pathway.腺病毒晚期基因表达不需要类似Rev的核RNA输出途径。
J Virol. 2000 Jul;74(14):6684-8. doi: 10.1128/jvi.74.14.6684-6688.2000.
2
Epstein-Barr virus EB2 protein exports unspliced RNA via a Crm-1-independent pathway.爱泼斯坦-巴尔病毒EB2蛋白通过一条不依赖Crm-1的途径输出未剪接的RNA。
J Virol. 2000 Jul;74(13):6068-76. doi: 10.1128/jvi.74.13.6068-6076.2000.
3
A comparison of the activity, sequence specificity, and CRM1-dependence of different nuclear export signals.不同核输出信号的活性、序列特异性及CRM1依赖性比较。
Exp Cell Res. 2000 Apr 10;256(1):213-24. doi: 10.1006/excr.2000.4825.
4
Evidence for specific nucleocytoplasmic transport pathways used by leucine-rich nuclear export signals.富含亮氨酸的核输出信号所使用的特定核质运输途径的证据。
Proc Natl Acad Sci U S A. 1999 May 25;96(11):6229-34. doi: 10.1073/pnas.96.11.6229.
5
A leptomycin B-sensitive homologue of human CRM1 promotes nuclear export of nuclear export sequence-containing proteins in Drosophila cells.人CRM1的一种对莱普霉素B敏感的同源物促进果蝇细胞中含核输出序列蛋白的核输出。
J Biol Chem. 2000 Jan 21;275(3):1878-86. doi: 10.1074/jbc.275.3.1878.
6
Anti-idiotype RNAs that mimic the leucine-rich nuclear export signal and specifically bind to CRM1/exportin 1.模拟富含亮氨酸的核输出信号并特异性结合CRM1/输出蛋白1的抗独特型RNA。
Chem Biol. 2000 May;7(5):345-54. doi: 10.1016/s1074-5521(00)00112-5.
7
Interactions between HIV Rev and nuclear import and export factors: the Rev nuclear localisation signal mediates specific binding to human importin-beta.HIV Rev与核输入和输出因子之间的相互作用:Rev核定位信号介导与人类输入蛋白β的特异性结合。
J Mol Biol. 1997 Dec 19;274(5):693-707. doi: 10.1006/jmbi.1997.1420.
8
The herpes simplex virus 1 Us11 protein cooperates with suboptimal amounts of human immunodeficiency virus type 1 (HIV-1) Rev protein to rescue HIV-1 production.单纯疱疹病毒1型Us11蛋白与次优量的1型人类免疫缺陷病毒(HIV-1)Rev蛋白协同作用,以挽救HIV-1的产生。
Virology. 2000 Apr 25;270(1):43-53. doi: 10.1006/viro.2000.0275.
9
Evaluating the role of CRM1-mediated export for adenovirus gene expression.评估CRM1介导的输出在腺病毒基因表达中的作用。
Virology. 2003 Oct 10;315(1):224-33. doi: 10.1016/s0042-6822(03)00526-9.
10
Inhibition of mRNA export in vertebrate cells by nuclear export signal conjugates.核输出信号偶联物对脊椎动物细胞中mRNA输出的抑制作用。
Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14394-9. doi: 10.1073/pnas.94.26.14394.

引用本文的文献

1
Global Transcriptome Analyses of Cellular and Viral mRNAs during HAdV-C5 Infection Highlight New Aspects of Viral mRNA Biogenesis and Cytoplasmic Viral mRNA Accumulations.HAdV-C5 感染过程中细胞和病毒 mRNA 的全球转录组分析突显了病毒 mRNA 生成和细胞质病毒 mRNA 积累的新方面。
Viruses. 2022 Nov 1;14(11):2428. doi: 10.3390/v14112428.
2
Nuclear imprisonment: viral strategies to arrest host mRNA nuclear export.核囚禁:病毒阻止宿主 mRNA 核输出的策略。
Viruses. 2013 Jul 18;5(7):1824-49. doi: 10.3390/v5071824.
3
CRM1-dependent transport supports cytoplasmic accumulation of adenoviral early transcripts.CRM1 依赖性运输支持腺病毒早期转录本在细胞质中的积累。
J Virol. 2012 Feb;86(4):2282-92. doi: 10.1128/JVI.06275-11. Epub 2011 Dec 14.
4
Role of the RNA recognition motif of the E1B 55 kDa protein in the adenovirus type 5 infectious cycle.E1B 55 kDa 蛋白的 RNA 识别模体在腺病毒 5 型感染周期中的作用。
Virology. 2011 Aug 15;417(1):9-17. doi: 10.1016/j.virol.2011.04.014. Epub 2011 May 24.
5
The E3 ubiquitin ligase activity associated with the adenoviral E1B-55K-E4orf6 complex does not require CRM1-dependent export.腺病毒 E1B-55K-E4orf6 复合物相关的 E3 泛素连接酶活性不需要 CRM1 依赖性输出。
J Virol. 2011 Jul;85(14):7081-94. doi: 10.1128/JVI.02368-10. Epub 2011 May 11.
6
Export of adenoviral late mRNA from the nucleus requires the Nxf1/Tap export receptor.腺病毒晚期 mRNA 从核内输出需要 Nxf1/Tap 输出受体。
J Virol. 2011 Feb;85(4):1429-38. doi: 10.1128/JVI.02108-10. Epub 2010 Dec 1.
7
Adenovirus E1B 55-kilodalton protein is required for both regulation of mRNA export and efficient entry into the late phase of infection in normal human fibroblasts.腺病毒E1B 55千道尔顿蛋白对于正常人类成纤维细胞中mRNA输出的调节以及高效进入感染后期都是必需的。
J Virol. 2006 Jan;80(2):964-74. doi: 10.1128/JVI.80.2.964-974.2006.
8
Effects of mutations in the adenoviral E1B 55-kilodalton protein coding sequence on viral late mRNA metabolism.腺病毒E1B 55千道尔顿蛋白编码序列突变对病毒晚期mRNA代谢的影响。
J Virol. 2002 May;76(9):4507-19. doi: 10.1128/jvi.76.9.4507-4519.2002.
9
E4orf6 variants with separate abilities to augment adenovirus replication and direct nuclear localization of the E1B 55-kilodalton protein.具有增强腺病毒复制和指导E1B 55千道尔顿蛋白核定位的不同能力的E4orf6变体。
J Virol. 2002 Feb;76(3):1475-87. doi: 10.1128/jvi.76.3.1475-1487.2002.
10
Degradation of p53 by adenovirus E4orf6 and E1B55K proteins occurs via a novel mechanism involving a Cullin-containing complex.腺病毒E4orf6和E1B55K蛋白对p53的降解通过一种涉及含Cullin复合物的新机制发生。
Genes Dev. 2001 Dec 1;15(23):3104-17. doi: 10.1101/gad.926401.

本文引用的文献

1
The nuclear export signal within the E4orf6 protein of adenovirus type 5 supports virus replication and cytoplasmic accumulation of viral mRNA.5型腺病毒E4orf6蛋白内的核输出信号支持病毒复制及病毒mRNA的细胞质积累。
J Virol. 2000 Jan;74(2):764-72. doi: 10.1128/jvi.74.2.764-772.2000.
2
Identification of novel import and export signals of human TAP, the protein that binds to the constitutive transport element of the type D retrovirus mRNAs.鉴定人类TAP的新型输入和输出信号,TAP是一种与D型逆转录病毒mRNA的组成型转运元件结合的蛋白质。
Mol Cell Biol. 1999 Sep;19(9):6306-17. doi: 10.1128/MCB.19.9.6306.
3
Cell biology. Snail mail to the nucleus.
Nature. 1999 May 20;399(6733):208-10. doi: 10.1038/20322.
4
RNA-binding activity of the E1B 55-kilodalton protein from human adenovirus type 5.来自人5型腺病毒的E1B 55千道尔顿蛋白的RNA结合活性
J Virol. 1998 Nov;72(11):9374-9. doi: 10.1128/JVI.72.11.9374-9379.1998.
5
E1B 55-kilodalton-associated protein: a cellular protein with RNA-binding activity implicated in nucleocytoplasmic transport of adenovirus and cellular mRNAs.E1B 55千道尔顿相关蛋白:一种具有RNA结合活性的细胞蛋白,与腺病毒和细胞信使核糖核酸的核质运输有关。
J Virol. 1998 Oct;72(10):7960-71. doi: 10.1128/JVI.72.10.7960-7971.1998.
6
Leptomycin B inhibition of signal-mediated nuclear export by direct binding to CRM1.细霉素B通过直接结合CRM1来抑制信号介导的核输出。
Exp Cell Res. 1998 Aug 1;242(2):540-7. doi: 10.1006/excr.1998.4136.
7
CRM1 is responsible for intracellular transport mediated by the nuclear export signal.CRM1负责由核输出信号介导的细胞内运输。
Nature. 1997 Nov 20;390(6657):308-11. doi: 10.1038/36894.
8
CRM1 is an export receptor for leucine-rich nuclear export signals.CRM1是富含亮氨酸的核输出信号的输出受体。
Cell. 1997 Sep 19;90(6):1051-60. doi: 10.1016/s0092-8674(00)80371-2.
9
Nuclear export receptors: from importin to exportin.核输出受体:从输入蛋白到输出蛋白
Cell. 1997 Sep 19;90(6):967-70. doi: 10.1016/s0092-8674(00)80361-x.
10
Nuclear export of the E1B 55-kDa and E4 34-kDa adenoviral oncoproteins mediated by a rev-like signal sequence.由类rev信号序列介导的E1B 55千道尔顿和E4 34千道尔顿腺病毒癌蛋白的核输出。
EMBO J. 1997 Jul 16;16(14):4276-84. doi: 10.1093/emboj/16.14.4276.