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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1995-2-17
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pubmed:abstractText |
HIV-1 genes are expressed through the complex splicing of a single mRNA precursor leading to three mRNA classes: unspliced, singly-spliced and multiply-spliced. Each class may include several mRNA species specifically encoding one or two HIV-1 proteins. Northern blotting and RT-PCR are the techniques currently used to analyse HIV-1 mRNA expression. Northern blotting allows quantitative detection of these three classes of viral RNA but does not discriminate between individual RNA species. RT-PCR allows discrimination between different species but does not provide a quantitative analysis. Here, we describe an application of an RNAse mapping assay which gives both quantitative and discriminative HIV-1 RNA detection. A radiolabeled probe overlapping the major splicing sites of HIV-1 used for the generation of HIV-1 mRNA subspecies was synthesized. This probe protects differential sizes of these species, allowing discrimination between them. We investigated the RNA expression pattern in high titer HIV-1 producing cells. The HIV-1-specific probe allowed the detection of multiply-spliced vpr, rev and nef mRNAs, singly-spliced env mRNA and unspliced genomic RNA. With its discriminative and quantitative properties, this application is particularly convenient for the investigation of HIV-1 mRNA expression during the course of HIV-1 infections.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleases
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0166-0934
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
9-23
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7829596-Base Sequence,
pubmed-meshheading:7829596-Blotting, Northern,
pubmed-meshheading:7829596-Cell Line,
pubmed-meshheading:7829596-Cloning, Molecular,
pubmed-meshheading:7829596-DNA, Viral,
pubmed-meshheading:7829596-DNA Primers,
pubmed-meshheading:7829596-Genes, Viral,
pubmed-meshheading:7829596-Genetic Vectors,
pubmed-meshheading:7829596-HIV-1,
pubmed-meshheading:7829596-Humans,
pubmed-meshheading:7829596-Molecular Sequence Data,
pubmed-meshheading:7829596-Nucleic Acid Hybridization,
pubmed-meshheading:7829596-Polymerase Chain Reaction,
pubmed-meshheading:7829596-RNA, Messenger,
pubmed-meshheading:7829596-RNA, Viral,
pubmed-meshheading:7829596-Ribonucleases,
pubmed-meshheading:7829596-Virology
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pubmed:year |
1994
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pubmed:articleTitle |
Quantitative and discriminative detection of individual HIV-1 mRNA subspecies by an RNAse mapping assay.
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pubmed:affiliation |
Unité mixte CNRS/Biomérieux, Lyon, France.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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