Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1992-12-14
pubmed:abstractText
Among eukaryotic transcription trans-activators, the human immunodeficiency virus type 1 (HIV-1) Tat protein is exceptional in that its target site TAR is an RNA rather than a DNA sequence. Here, we confirm that fusion of Tat to the RNA-binding domain of the HIV-1 Rev protein permits the efficient activation of an HIV-1 long terminal repeat (LTR) promoter in which critical TAR sequences have been replaced by RNA sequences derived from the HIV-1 Rev response element (RRE). An RRE target sequence as small as 13 nucleotides is shown to form an effective in vivo target for Rev binding. More important, a fusion protein consisting of Rev attached to the VP16 transcription activation domain was also observed to efficiently activate the HIV-1 LTR from this nascent RNA target. These data demonstrate that trans-activation of transcription by acidic activation domains does not require a stable interaction with the promoter DNA and suggest that VP16, like Tat, can act on steps subsequent to the formation of the HIV-1 LTR preinitiation complex. The finding that the activation domains of VP16 and Tat are functionally interchangeable raises the possibility that these apparently disparate viral trans-activators may nevertheless act via similar mechanisms.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0890-9369
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2077-87
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:1427073-Base Sequence, pubmed-meshheading:1427073-Binding Sites, pubmed-meshheading:1427073-Cell Line, pubmed-meshheading:1427073-Chloramphenicol O-Acetyltransferase, pubmed-meshheading:1427073-Gene Products, rev, pubmed-meshheading:1427073-Gene Products, tat, pubmed-meshheading:1427073-Genes, rev, pubmed-meshheading:1427073-Genes, tat, pubmed-meshheading:1427073-HIV Long Terminal Repeat, pubmed-meshheading:1427073-HIV-1, pubmed-meshheading:1427073-HeLa Cells, pubmed-meshheading:1427073-Humans, pubmed-meshheading:1427073-Molecular Sequence Data, pubmed-meshheading:1427073-Nucleic Acid Conformation, pubmed-meshheading:1427073-Oligodeoxyribonucleotides, pubmed-meshheading:1427073-Promoter Regions, Genetic, pubmed-meshheading:1427073-RNA, Viral, pubmed-meshheading:1427073-Restriction Mapping, pubmed-meshheading:1427073-Trans-Activators, pubmed-meshheading:1427073-Transcriptional Activation, pubmed-meshheading:1427073-rev Gene Products, Human Immunodeficiency Virus, pubmed-meshheading:1427073-tat Gene Products, Human Immunodeficiency Virus
pubmed:year
1992
pubmed:articleTitle
The VP16 transcription activation domain is functional when targeted to a promoter-proximal RNA sequence.
pubmed:affiliation
Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't