中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Functional domains and the antiviral effect of the double-stranded RNA-dependent protein kinase PKR from Paralichthys olivaceus

文献类型:期刊论文

作者Zhu, Rong; Zhang, Yi-Bing; Zhang, Qi-Ya; Gui, Jian-Fang
刊名JOURNAL OF VIROLOGY
出版日期2008-07-01
卷号82期号:14页码:6889-6901
关键词INITIATION FACTOR-II TRANSLATIONAL CONTROL MOLECULAR-CLONING BINDING DOMAINS CAB CELLS EUKARYOTIC INITIATION-FACTOR-2-ALPHA MESSENGER-RNAS ALPHA-SUBUNIT INTERFERON VIRUS
ISSN号0022-538X
通讯作者Gui, JF, Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Grad Sch, Wuhan 430072, Peoples R China
中文摘要The double-stranded RNA (dsRNA)-dependent protein kinase PKR is thought to mediate a conserved antiviral pathway by inhibiting viral protein synthesis via the phosphorylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2 alpha). However, little is known about the data related to the lower vertebrates, including fish. Recently, the identification of PKR-like, or PKZ, has addressed the question of whether there is an orthologous PKR in fish. Here, we identify the first fish PKR gene from the Japanese flounder Paralichthys olivaceus (PoPKR). PoPKR encodes a protein that shows a conserved structure that is characteristic of mammalian PKRs, having both the N-terminal region for dsRNA binding and the C-terminal region for the inhibition of protein translation. The catalytic activity of PoPKR is further evidence that it is required for protein translation inhibition in vitro. PoPKR is constitutively transcribed at low levels and is highly induced after virus infection. Strikingly, PoPKR overexpression increases eIF2 alpha phosphorylation and inhibits the replication of Scophthalmus maximus rhabdovirus (SMRV) in flounder embryonic cells, whereas phosphorylation and antiviral effects are impaired in transfected cells expressing the catalytically inactive PKR-K421R variant, indicating that PoPKR inhibits virus replication by phosphorylating substrate eIF2 alpha. The interaction between PoPKR and eIF2 alpha is demonstrated by coimmunoprecipitation assays, and the transfection of PoPKR-specific short interfering RNA further reveals that the enhanced eIF2 alpha phosphorylation is catalyzed by PoPKR during SMRV infection. The current data provide significant evidence for the existence of a PKR-mediated antiviral pathway in fish and reveal considerable conservation in the functional domains and the antiviral effect of PKR proteins between fish and mammals.
英文摘要The double-stranded RNA (dsRNA)-dependent protein kinase PKR is thought to mediate a conserved antiviral pathway by inhibiting viral protein synthesis via the phosphorylation of the alpha subunit of eukaryotic initiation factor 2 (eIF2 alpha). However, little is known about the data related to the lower vertebrates, including fish. Recently, the identification of PKR-like, or PKZ, has addressed the question of whether there is an orthologous PKR in fish. Here, we identify the first fish PKR gene from the Japanese flounder Paralichthys olivaceus (PoPKR). PoPKR encodes a protein that shows a conserved structure that is characteristic of mammalian PKRs, having both the N-terminal region for dsRNA binding and the C-terminal region for the inhibition of protein translation. The catalytic activity of PoPKR is further evidence that it is required for protein translation inhibition in vitro. PoPKR is constitutively transcribed at low levels and is highly induced after virus infection. Strikingly, PoPKR overexpression increases eIF2 alpha phosphorylation and inhibits the replication of Scophthalmus maximus rhabdovirus (SMRV) in flounder embryonic cells, whereas phosphorylation and antiviral effects are impaired in transfected cells expressing the catalytically inactive PKR-K421R variant, indicating that PoPKR inhibits virus replication by phosphorylating substrate eIF2 alpha. The interaction between PoPKR and eIF2 alpha is demonstrated by coimmunoprecipitation assays, and the transfection of PoPKR-specific short interfering RNA further reveals that the enhanced eIF2 alpha phosphorylation is catalyzed by PoPKR during SMRV infection. The current data provide significant evidence for the existence of a PKR-mediated antiviral pathway in fish and reveal considerable conservation in the functional domains and the antiviral effect of PKR proteins between fish and mammals.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
学科主题Virology
类目[WOS]Virology
研究领域[WOS]Virology
关键词[WOS]INITIATION FACTOR-II ; TRANSLATIONAL CONTROL ; MOLECULAR-CLONING ; BINDING DOMAINS ; CAB CELLS ; EUKARYOTIC INITIATION-FACTOR-2-ALPHA ; MESSENGER-RNAS ; ALPHA-SUBUNIT ; INTERFERON ; VIRUS
收录类别SCI
语种英语
WOS记录号WOS:000257545300011
公开日期2010-10-13
源URL[http://ir.ihb.ac.cn/handle/152342/8062]  
专题水生生物研究所_中科院水生所知识产出(2009年前)_期刊论文
作者单位Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Grad Sch, Wuhan 430072, Peoples R China
推荐引用方式
GB/T 7714
Zhu, Rong,Zhang, Yi-Bing,Zhang, Qi-Ya,et al. Functional domains and the antiviral effect of the double-stranded RNA-dependent protein kinase PKR from Paralichthys olivaceus[J]. JOURNAL OF VIROLOGY,2008,82(14):6889-6901.
APA Zhu, Rong,Zhang, Yi-Bing,Zhang, Qi-Ya,&Gui, Jian-Fang.(2008).Functional domains and the antiviral effect of the double-stranded RNA-dependent protein kinase PKR from Paralichthys olivaceus.JOURNAL OF VIROLOGY,82(14),6889-6901.
MLA Zhu, Rong,et al."Functional domains and the antiviral effect of the double-stranded RNA-dependent protein kinase PKR from Paralichthys olivaceus".JOURNAL OF VIROLOGY 82.14(2008):6889-6901.

入库方式: OAI收割

来源:水生生物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。