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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1997-6-20
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pubmed:abstractText |
JC virus lacks an appropriate cell line to support virus replication. The establishment of a JC pseudovirus assembly system could play an alternative role for a virus culture system. COS7 cells and a transfer vector, pcDL-SR alpha 296, were used to express JC viral structural genes. VP231-SR alpha, which encodes VP2/VP3 and VP1, but lacks 137 bp of the 5'-terminus of agnogene, showed both efficient nuclear migration and quantitative expression of the major capsid protein VP1. JC pseudovirus assembly was observed in the nucleus of VP231-SR alpha transfected cells. Evidence of JC pseudovirus assembly is presented. The further utilization of this system, which includes a study for the viral morphogenesis, serological diagnosis, as well as the potential application for gene transfer vector, is discussed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0146-6615
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
265-72
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9093939-Animals,
pubmed-meshheading:9093939-COS Cells,
pubmed-meshheading:9093939-Capsid,
pubmed-meshheading:9093939-Capsid Proteins,
pubmed-meshheading:9093939-Cell Nucleus,
pubmed-meshheading:9093939-Humans,
pubmed-meshheading:9093939-JC Virus,
pubmed-meshheading:9093939-Virion,
pubmed-meshheading:9093939-Virus Assembly
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pubmed:year |
1997
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pubmed:articleTitle |
Assembly of JC virus-like particles in COS7 cells.
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pubmed:affiliation |
Department of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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