中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Cloning, expression and subcellular distribution of a Rana grylio virus late gene encoding ERV1 homologue

文献类型:期刊论文

作者Ke, Fei; Zhao, Zhe; Zhang, Qiya
刊名MOLECULAR BIOLOGY REPORTS
出版日期2009-09-01
卷号36期号:7页码:1651-1659
关键词Rana grylio virus (RGV) Iridovirus ERV1 Late viral gene RNAi
ISSN号0301-4851
通讯作者Zhang, QY, Chinese Acad Sci, State Key Lab Freshwater Ecol & Biotechnol, Inst Hydrobiol, Grad Sch, Wuhan 430072, Peoples R China
中文摘要An essential for respiration and viability (ERV1) homologue, 88R, was cloned and characterized from Rana grylio virus (RGV). Database searches found its homologues in all sequenced iridoviruses, and sequence alignment revealed a highly conserved motif shared by all ERV1 family proteins: Cys-X-X-Cys. RT-PCR and western blot analysis revealed that 88R begins to transcribe and translate at 6 h postinfection (p.i.) and remains detectable at 48 h p.i. during RGV infection course. Furthermore, using drug inhibition analysis by a de novo protein synthesis inhibitor and a viral DNA replication inhibitor, RGV 88R was classified as a late (L) viral gene during the in vitro infection. 88R-EGFP fusion protein was observed in both the cytoplasm and nucleus of pEGFP-N3-88R transfected EPC cells. Although result of immunofluorescence is similar, 88R protein was not detected in viromatrix. Moreover, function of RGV 88R on virus replication were evaluated by RNAi assay. Nevertheless, effect of knockdown of RGV 88R expression on virus replication was not detected in cultured fish cell lines. Collectively, current data indicate that RGV 88R was a late gene of iridovirus encoding protein that distributed both the cytoplasm and nucleus.
英文摘要An essential for respiration and viability (ERV1) homologue, 88R, was cloned and characterized from Rana grylio virus (RGV). Database searches found its homologues in all sequenced iridoviruses, and sequence alignment revealed a highly conserved motif shared by all ERV1 family proteins: Cys-X-X-Cys. RT-PCR and western blot analysis revealed that 88R begins to transcribe and translate at 6 h postinfection (p.i.) and remains detectable at 48 h p.i. during RGV infection course. Furthermore, using drug inhibition analysis by a de novo protein synthesis inhibitor and a viral DNA replication inhibitor, RGV 88R was classified as a late (L) viral gene during the in vitro infection. 88R-EGFP fusion protein was observed in both the cytoplasm and nucleus of pEGFP-N3-88R transfected EPC cells. Although result of immunofluorescence is similar, 88R protein was not detected in viromatrix. Moreover, function of RGV 88R on virus replication were evaluated by RNAi assay. Nevertheless, effect of knockdown of RGV 88R expression on virus replication was not detected in cultured fish cell lines. Collectively, current data indicate that RGV 88R was a late gene of iridovirus encoding protein that distributed both the cytoplasm and nucleus.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
学科主题Biochemistry & Molecular Biology
类目[WOS]Biochemistry & Molecular Biology
研究领域[WOS]Biochemistry & Molecular Biology
关键词[WOS]MULTIPLE SEQUENCE ALIGNMENT ; FISH CELL-LINE ; FAMILY IRIDOVIRIDAE ; NONSTRUCTURAL PROTEIN ; RNA INTERFERENCE ; IRIDESCENT VIRUS ; THIOREDOXIN ; INHIBITION ; MORPHOGENESIS ; TRANSCRIPTION
收录类别SCI
资助信息National Major Basic Research Program [2004CB117403]; National 863 High Technology Research Foundation of China [2006AA09Z445, 2006AA100309, 20060110A4013]; National Natural Science Foundation of China [30671616, U0631008]; Key Technology R & D Program of China [2006BAD03B05]
语种英语
WOS记录号WOS:000268496800002
公开日期2010-10-13
源URL[http://ir.ihb.ac.cn/handle/152342/7628]  
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, State Key Lab Freshwater Ecol & Biotechnol, Inst Hydrobiol, Grad Sch, Wuhan 430072, Peoples R China
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Ke, Fei,Zhao, Zhe,Zhang, Qiya. Cloning, expression and subcellular distribution of a Rana grylio virus late gene encoding ERV1 homologue[J]. MOLECULAR BIOLOGY REPORTS,2009,36(7):1651-1659.
APA Ke, Fei,Zhao, Zhe,&Zhang, Qiya.(2009).Cloning, expression and subcellular distribution of a Rana grylio virus late gene encoding ERV1 homologue.MOLECULAR BIOLOGY REPORTS,36(7),1651-1659.
MLA Ke, Fei,et al."Cloning, expression and subcellular distribution of a Rana grylio virus late gene encoding ERV1 homologue".MOLECULAR BIOLOGY REPORTS 36.7(2009):1651-1659.

入库方式: OAI收割

来源:水生生物研究所

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