• 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

腮腺炎病毒结构V蛋白的C末端富含半胱氨酸区域通过降低信号转导和转录激活因子1α(STAT 1-α)与干扰素α和γ信号转导途径的阻断相关。

C terminal CYS-RICH region of mumps virus structural V protein correlates with block of interferon alpha and gamma signal transduction pathway through decrease of STAT 1-alpha.

作者信息

Kubota T, Yokosawa N, Yokota S, Fujii N

机构信息

Department of Microbiology, Sapporo Medical University School of Medicine, South 1, West 16, Chou-ku, Sapporo, Hokkaido, 060-8556, Japan.

出版信息

Biochem Biophys Res Commun. 2001 Apr 27;283(1):255-9. doi: 10.1006/bbrc.2001.4764.

DOI:10.1006/bbrc.2001.4764
PMID:11322797
Abstract

It has been reported that interferon (IFN)-alpha/gamma signal transduction pathway is blocked in several cell lines persistently infected with mumps virus (MV) through decrease of STAT-1alpha. Expression of the MV structural V protein (MV-V) or C terminal CYS-RICH region of the V protein (MV-Vsp) inhibited the establishment of the antivirus state induced by IFN, but not by expression of the MV-P protein. Suppression of IFN-induced STAT-1alpha, STAT-2, and IRF-9 (p48) induction was also recognized in the cells transfected with expression vector of the MV-V (pTM-V) or MV-Vsp (pTM-Vsp) protein, even though it was in the absence of the other virus protein. It is supposed that the cysteine-rich domain of V protein (Vsp) is involved in the suppression of the IFN signal transduction pathway.

摘要

据报道,在几种持续感染腮腺炎病毒(MV)的细胞系中,由于STAT-1α的减少,干扰素(IFN)-α/γ信号转导途径被阻断。MV结构V蛋白(MV-V)或V蛋白的C末端富含半胱氨酸区域(MV-Vsp)的表达抑制了IFN诱导的抗病毒状态的建立,但MV-P蛋白的表达则没有这种作用。在用MV-V(pTM-V)或MV-Vsp(pTM-Vsp)蛋白表达载体转染的细胞中,也观察到IFN诱导的STAT-1α、STAT-2和IRF-9(p48)诱导的抑制,即使不存在其他病毒蛋白。推测V蛋白(Vsp)的富含半胱氨酸结构域参与了IFN信号转导途径的抑制。

相似文献

1
C terminal CYS-RICH region of mumps virus structural V protein correlates with block of interferon alpha and gamma signal transduction pathway through decrease of STAT 1-alpha.腮腺炎病毒结构V蛋白的C末端富含半胱氨酸区域通过降低信号转导和转录激活因子1α(STAT 1-α)与干扰素α和γ信号转导途径的阻断相关。
Biochem Biophys Res Commun. 2001 Apr 27;283(1):255-9. doi: 10.1006/bbrc.2001.4764.
2
Mumps virus can suppress the effective augmentation of HPC-induced apoptosis by IFN-gamma through disruption of IFN signaling in U937 cells.腮腺炎病毒可通过破坏U937细胞中的IFN信号传导,抑制IFN-γ对HPC诱导的细胞凋亡的有效增强作用。
Microbiol Immunol. 2000;44(6):537-41. doi: 10.1111/j.1348-0421.2000.tb02531.x.
3
Association of mumps virus V protein with RACK1 results in dissociation of STAT-1 from the alpha interferon receptor complex.腮腺炎病毒V蛋白与RACK1的结合导致STAT-1从α干扰素受体复合物上解离。
J Virol. 2002 Dec;76(24):12676-82. doi: 10.1128/jvi.76.24.12676-12682.2002.
4
A selective defect of IFN-gamma- but not of IFN-alpha-induced JAK/STAT pathway in a subset of U937 clones prevents the antiretroviral effect of IFN-gamma against HIV-1.U937克隆亚群中存在IFN-γ诱导的JAK/STAT途径的选择性缺陷,而非IFN-α诱导的JAK/STAT途径的缺陷,这阻止了IFN-γ对HIV-1的抗逆转录病毒作用。
J Immunol. 1999 Jan 1;162(1):323-30.
5
Nipah virus V protein evades alpha and gamma interferons by preventing STAT1 and STAT2 activation and nuclear accumulation.尼帕病毒V蛋白通过阻止信号转导和转录激活因子1(STAT1)和信号转导和转录激活因子2(STAT2)的激活及核内积累来逃避α和γ干扰素。
J Virol. 2002 Nov;76(22):11476-83. doi: 10.1128/jvi.76.22.11476-11483.2002.
6
C-terminal region of STAT-1alpha is not necessary for its ubiquitination and degradation caused by mumps virus V protein.STAT-1α的C末端区域对于腮腺炎病毒V蛋白引起的其泛素化和降解并非必需。
J Virol. 2002 Dec;76(24):12683-90. doi: 10.1128/jvi.76.24.12683-12690.2002.
7
The V protein of human parainfluenza virus 2 antagonizes type I interferon responses by destabilizing signal transducer and activator of transcription 2.人副流感病毒2型的V蛋白通过使信号转导子和转录激活子2不稳定来拮抗I型干扰素反应。
Virology. 2001 May 10;283(2):230-9. doi: 10.1006/viro.2001.0856.
8
Inhibition of interferon-stimulated JAK-STAT signaling by a tick-borne flavivirus and identification of NS5 as an interferon antagonist.一种蜱传黄病毒对干扰素刺激的JAK-STAT信号通路的抑制作用以及NS5作为干扰素拮抗剂的鉴定。
J Virol. 2005 Oct;79(20):12828-39. doi: 10.1128/JVI.79.20.12828-12839.2005.
9
The V protein of simian virus 5 inhibits interferon signalling by targeting STAT1 for proteasome-mediated degradation.猴病毒5的V蛋白通过将信号转导和转录激活因子1(STAT1)作为蛋白酶体介导降解的靶点来抑制干扰素信号传导。
J Virol. 1999 Dec;73(12):9928-33. doi: 10.1128/JVI.73.12.9928-9933.1999.
10
Degradation of STAT1 and STAT2 by the V proteins of simian virus 5 and human parainfluenza virus type 2, respectively: consequences for virus replication in the presence of alpha/beta and gamma interferons.猿猴病毒5和人副流感病毒2的V蛋白分别对信号转导和转录激活因子1(STAT1)及信号转导和转录激活因子2(STAT2)的降解作用:在α/β干扰素和γ干扰素存在的情况下对病毒复制的影响
J Virol. 2002 Mar;76(5):2159-67. doi: 10.1128/jvi.76.5.2159-2167.2002.

引用本文的文献

1
Transcription Factors and Methods for the Pharmacological Correction of Their Activity.转录因子及其活性的药理学校正方法。
Int J Mol Sci. 2025 Jul 2;26(13):6394. doi: 10.3390/ijms26136394.
2
Human metapneumovirus SH protein promotes JAK1 degradation to impair host IL-6 signaling.人偏肺病毒SH蛋白促进JAK1降解以损害宿主IL-6信号传导。
J Virol. 2024 Nov 19;98(11):e0110424. doi: 10.1128/jvi.01104-24. Epub 2024 Oct 16.
3
Human metapneumovirus SH protein promotes JAK1 degradation to impair host IL-6 signaling.人偏肺病毒SH蛋白促进JAK1降解,损害宿主IL-6信号通路。
bioRxiv. 2024 May 14:2024.05.10.593594. doi: 10.1101/2024.05.10.593594.
4
Oncolytic viruses against cancer, promising or delusion?溶瘤病毒治疗癌症:有希望还是妄想?
Med Oncol. 2023 Jul 17;40(8):246. doi: 10.1007/s12032-023-02106-6.
5
Type I and Type II Interferon Antagonism Strategies Used by : Previous and New Discoveries, in Comparison.I 型和 II 型干扰素拮抗策略的比较:旧发现与新发现。
Viruses. 2022 May 21;14(5):1107. doi: 10.3390/v14051107.
6
Mumps Vaccines: Current Challenges and Future Prospects.腮腺炎疫苗:当前挑战与未来前景
Front Microbiol. 2020 Aug 20;11:1999. doi: 10.3389/fmicb.2020.01999. eCollection 2020.
7
Lyssavirus P-protein selectively targets STAT3-STAT1 heterodimers to modulate cytokine signalling.狂犬病毒 P 蛋白选择性地靶向 STAT3-STAT1 异二聚体,从而调节细胞因子信号。
PLoS Pathog. 2020 Sep 9;16(9):e1008767. doi: 10.1371/journal.ppat.1008767. eCollection 2020 Sep.
8
The Dynamic Interface of Viruses with STATs.病毒与 STATs 的动态界面。
J Virol. 2020 Oct 27;94(22). doi: 10.1128/JVI.00856-20.
9
The Intrinsically Disordered W Protein Is Multifunctional during Henipavirus Infection, Disrupting Host Signalling Pathways and Nuclear Import.固有无序 W 蛋白在亨尼帕病毒感染过程中具有多功能性,可破坏宿主信号通路和核输入。
Cells. 2020 Aug 18;9(8):1913. doi: 10.3390/cells9081913.
10
A Single Point Mutation in the Mumps V Protein Alters Targeting of the Cellular STAT Pathways Resulting in Virus Attenuation.一个在腮腺炎病毒 V 蛋白中的单点突变改变了细胞 STAT 途径的靶向,导致病毒减毒。
Viruses. 2019 Nov 1;11(11):1016. doi: 10.3390/v11111016.