Characterization of grass carp reovirus minor core protein VP4

<p>Abstract</p> <p>Background</p> <p>Grass Carp Reovirus (GCRV), a tentative member in the genus <it>Aquareovirus</it> of family <it>Reoviridae</it>, contains eleven segmented (double-stranded RNA<b>)</b> dsRNA genome which encodes 12...

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Main Authors: Yan Liming, Guo Hong, Sun Xiaoyun, Shao Ling, Fang Qin
Format: Article
Language:English
Published: BMC 2012-07-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/9/1/89
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spelling doaj-d5d62ba2cfc74b678be89bb01033f20f2020-11-25T00:15:22ZengBMCVirology Journal1743-422X2012-07-01918910.1186/1743-422X-9-89Characterization of grass carp reovirus minor core protein VP4Yan LimingGuo HongSun XiaoyunShao LingFang Qin<p>Abstract</p> <p>Background</p> <p>Grass Carp Reovirus (GCRV), a tentative member in the genus <it>Aquareovirus</it> of family <it>Reoviridae</it>, contains eleven segmented (double-stranded RNA<b>)</b> dsRNA genome which encodes 12 proteins. A low-copy core component protein VP4, encoded by the viral genome segment 5(S5), has been suggested to play a key role in viral genome transcription and replication.</p> <p>Results</p> <p>To understand the role of minor core protein VP4 played in molecular pathogenesis during GCRV infection, the recombinant GCRV VP4 gene was constructed and expressed in both prokaryotic and mammalian cells in this investigation. The recombinant His-tag fusion VP4 products expressed in E.<it>coli</it> were identified by Western blotting utilizing His-tag specific monoclonal and GCRV polyclonal antibodies. In addition, the expression of VP4 in GCRV infected cells, appeared in granules structure concentrated mainly in the cytoplasm, can be detected by Immunofluorescence (IF) using prepared anti-VP4 polyclonal antibody. Meanwhile, VP4 protein in GCRV core and infected cell lysate was identified by Immunoblotting (IB) assay. Of particular note, the VP4 protein was exhibited a diffuse distribution in the cytoplasm and nucleus in transfected cells, suggesting that VP4 protein may play a partial role in the nucleus by regulating cell cycle besides its predicted cytoplasmic function in GCRV infection.</p> <p>Conclusions</p> <p>Our results indicate the VP4 is a core component in GCRV. The cellular localization of VP4 is correlated with its predicted function. The data provide a foundation for further studies aimed at understanding the role of VP4 in viroplasmic inclusion bodies (VIB) formation during GCRV replication and assembly.</p> http://www.virologyj.com/content/9/1/89
collection DOAJ
language English
format Article
sources DOAJ
author Yan Liming
Guo Hong
Sun Xiaoyun
Shao Ling
Fang Qin
spellingShingle Yan Liming
Guo Hong
Sun Xiaoyun
Shao Ling
Fang Qin
Characterization of grass carp reovirus minor core protein VP4
Virology Journal
author_facet Yan Liming
Guo Hong
Sun Xiaoyun
Shao Ling
Fang Qin
author_sort Yan Liming
title Characterization of grass carp reovirus minor core protein VP4
title_short Characterization of grass carp reovirus minor core protein VP4
title_full Characterization of grass carp reovirus minor core protein VP4
title_fullStr Characterization of grass carp reovirus minor core protein VP4
title_full_unstemmed Characterization of grass carp reovirus minor core protein VP4
title_sort characterization of grass carp reovirus minor core protein vp4
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2012-07-01
description <p>Abstract</p> <p>Background</p> <p>Grass Carp Reovirus (GCRV), a tentative member in the genus <it>Aquareovirus</it> of family <it>Reoviridae</it>, contains eleven segmented (double-stranded RNA<b>)</b> dsRNA genome which encodes 12 proteins. A low-copy core component protein VP4, encoded by the viral genome segment 5(S5), has been suggested to play a key role in viral genome transcription and replication.</p> <p>Results</p> <p>To understand the role of minor core protein VP4 played in molecular pathogenesis during GCRV infection, the recombinant GCRV VP4 gene was constructed and expressed in both prokaryotic and mammalian cells in this investigation. The recombinant His-tag fusion VP4 products expressed in E.<it>coli</it> were identified by Western blotting utilizing His-tag specific monoclonal and GCRV polyclonal antibodies. In addition, the expression of VP4 in GCRV infected cells, appeared in granules structure concentrated mainly in the cytoplasm, can be detected by Immunofluorescence (IF) using prepared anti-VP4 polyclonal antibody. Meanwhile, VP4 protein in GCRV core and infected cell lysate was identified by Immunoblotting (IB) assay. Of particular note, the VP4 protein was exhibited a diffuse distribution in the cytoplasm and nucleus in transfected cells, suggesting that VP4 protein may play a partial role in the nucleus by regulating cell cycle besides its predicted cytoplasmic function in GCRV infection.</p> <p>Conclusions</p> <p>Our results indicate the VP4 is a core component in GCRV. The cellular localization of VP4 is correlated with its predicted function. The data provide a foundation for further studies aimed at understanding the role of VP4 in viroplasmic inclusion bodies (VIB) formation during GCRV replication and assembly.</p>
url http://www.virologyj.com/content/9/1/89
work_keys_str_mv AT yanliming characterizationofgrasscarpreovirusminorcoreproteinvp4
AT guohong characterizationofgrasscarpreovirusminorcoreproteinvp4
AT sunxiaoyun characterizationofgrasscarpreovirusminorcoreproteinvp4
AT shaoling characterizationofgrasscarpreovirusminorcoreproteinvp4
AT fangqin characterizationofgrasscarpreovirusminorcoreproteinvp4
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