Identification, cloning, and expression of the major capsid protein gene of human herpesvirus 6.
dc.contributor.author | Littler, Edward | |
dc.contributor.author | Lawrence, G | |
dc.contributor.author | Liu, Mei-Ying | |
dc.contributor.author | Barrell, B G | |
dc.contributor.author | Arrand, John R | |
dc.date.accessioned | 2010-08-18T08:23:55Z | |
dc.date.available | 2010-08-18T08:23:55Z | |
dc.date.issued | 1990-02 | |
dc.identifier.citation | Identification, cloning, and expression of the major capsid protein gene of human herpesvirus 6. 1990, 64 (2):714-22 J. Virol. | en |
dc.identifier.issn | 0022-538X | |
dc.identifier.pmid | 2153237 | |
dc.identifier.uri | http://hdl.handle.net/10541/109813 | |
dc.description.abstract | DNA sequence analysis of part of the human herpesvirus 6 (HHV-6) genome led to the identification of an open reading frame with amino acid sequence homology to the major capsid proteins (MCP) of other HHVs. DIAGON analysis showed that the closest homology was with human cytomegalovirus. Plasmids were constructed which were shown to express the HHV-6 MCP as either the entire open reading frame or as portions of it, and the recombinant-produced proteins were used to raise antisera. The antisera were shown by immunofluorescence to react with HHV-6-infected lymphoblastoid cells and in Western blots with a 135-kilodalton protein specific to HHV-6-infected cells. The recombinant protein expressed from the entire HHV-6 MCP gene was detected only weakly in Western blot assays with normal HHV-6-positive human sera as a probe. | |
dc.language.iso | en | en |
dc.subject.mesh | Amino Acid Sequence | |
dc.subject.mesh | Base Sequence | |
dc.subject.mesh | Capsid | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | Cloning, Molecular | |
dc.subject.mesh | DNA, Viral | |
dc.subject.mesh | Fetal Blood | |
dc.subject.mesh | Gene Expression | |
dc.subject.mesh | Genes, Viral | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lymphocytes | |
dc.subject.mesh | Molecular Sequence Data | |
dc.subject.mesh | Plasmids | |
dc.subject.mesh | Restriction Mapping | |
dc.subject.mesh | Sequence Homology, Nucleic Acid | |
dc.subject.mesh | Simplexvirus | |
dc.subject.mesh | Viral Structural Proteins | |
dc.title | Identification, cloning, and expression of the major capsid protein gene of human herpesvirus 6. | en |
dc.type | Article | en |
dc.contributor.department | Department of Molecular Biology, Christie Hospital & Holt Radium Institute, Manchester, United Kingdom. | en |
dc.identifier.journal | Journal of Virology | en |
html.description.abstract | DNA sequence analysis of part of the human herpesvirus 6 (HHV-6) genome led to the identification of an open reading frame with amino acid sequence homology to the major capsid proteins (MCP) of other HHVs. DIAGON analysis showed that the closest homology was with human cytomegalovirus. Plasmids were constructed which were shown to express the HHV-6 MCP as either the entire open reading frame or as portions of it, and the recombinant-produced proteins were used to raise antisera. The antisera were shown by immunofluorescence to react with HHV-6-infected lymphoblastoid cells and in Western blots with a 135-kilodalton protein specific to HHV-6-infected cells. The recombinant protein expressed from the entire HHV-6 MCP gene was detected only weakly in Western blot assays with normal HHV-6-positive human sera as a probe. |