rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
1994-10-18
|
pubmed:abstractText |
The 5'-TAR region of HIV-1 mRNA is highly conserved amongst different HIV-1 isolates. We thus investigated the potential for in vivo targeting of the TAR RNA element by a hammerhead ribozyme. The use of the CAT reporter gene linked to the HIV1-LTR, in transient assays, reveals that a hammerhead ribozyme directed towards the first GUC of HIV-1 mRNA can efficiently inhibit CAT protein expression. We show that this inhibition is sequence-specific and probably due to a cleavage activity rather than an antisense effect. We show also that a hammerhead ribozyme that is inactive in vitro is capable of inhibiting CAT protein expression in a cellular environment. These results suggest that the targeting of the HIV-1 LTR by a hammerhead ribozyme constitutes a viable approach for anti-HIV therapy.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Sep
|
pubmed:issn |
0006-291X
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
203
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
889-98
|
pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8093072-Base Sequence,
pubmed-meshheading:8093072-Cell Line,
pubmed-meshheading:8093072-Chloramphenicol O-Acetyltransferase,
pubmed-meshheading:8093072-Gene Expression,
pubmed-meshheading:8093072-Gene Products, tat,
pubmed-meshheading:8093072-Genes, Reporter,
pubmed-meshheading:8093072-HIV Long Terminal Repeat,
pubmed-meshheading:8093072-HIV-1,
pubmed-meshheading:8093072-Molecular Sequence Data,
pubmed-meshheading:8093072-Plasmids,
pubmed-meshheading:8093072-RNA, Catalytic,
pubmed-meshheading:8093072-RNA, Messenger,
pubmed-meshheading:8093072-Transfection,
pubmed-meshheading:8093072-tat Gene Products, Human Immunodeficiency Virus
|
pubmed:year |
1994
|
pubmed:articleTitle |
Ribozyme targeting of HIV-1 LTR.
|
pubmed:affiliation |
ICGM, INSERM U 363, Université Paris V, Hospital Cochin, Paris, France.
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pubmed:publicationType |
Journal Article
|