The HIV-1 long terminal repeat contains an unusual element that induces the synthesis of short RNAs from various mRNA and snRNA promoters.

Details

Serval ID
serval:BIB_12BEFCA45A3A
Type
Article: article from journal or magazin.
Collection
Publications
Title
The HIV-1 long terminal repeat contains an unusual element that induces the synthesis of short RNAs from various mRNA and snRNA promoters.
Journal
Genes and Development
Author(s)
Ratnasabapathy R., Sheldon M., Johal L., Hernandez N.
ISSN
0890-9369[print], 0890-9369[linking]
Publication state
Published
Issued date
12/1990
Volume
4
Number
12A
Pages
2061-2074
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Abstract
We describe an unusual element that activates the synthesis of short transcripts from a wide variety of mRNA and small nuclear RNA (snRNA) promoters, including the U6 RNA polymerase III promoter. This inducer of short transcripts (IST) is located between positions -5 and +82 relative to the cap site in the HIV-1 LTR. In the presence of IST, the total transcriptional activity of the different promoters is greatly increased, but the resulting additional RNA molecules are short, ending around position +60. IST is not the RNA target (TAR) for Tat trans-activation; however, because it relies entirely on cellular factors for activity, IST may serve to provide abundant RNA targets for Tat trans-activation without a requirement for full-length viral mRNA expression.
Keywords
Base Sequence, Genes, tat, HIV Long Terminal Repeat, HIV-1/genetics, Molecular Sequence Data, Nucleic Acid Conformation, Promoter Regions, Genetic, RNA Polymerase II/genetics, RNA Polymerase II/metabolism, RNA Polymerase III/genetics, RNA Polymerase III/metabolism, RNA, Messenger/metabolism, RNA, Small Nuclear/genetics, RNA, Viral/biosynthesis, Restriction Mapping, Transcription, Genetic, Transcriptional Activation
Pubmed
Web of science
Open Access
Yes
Create date
21/01/2008 16:34
Last modification date
20/08/2019 12:41
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