Evidence map›Paper›PMID 10233987›Full record

ArticleJournal of virology1999

Potent inhibition of human immunodeficiency virus type 1 (HIV-1) gene expression and virus production by an HIV-2 tat activation-response RNA decoy.

C M Browning, L Cagnon, P D Good, J Rossi, D R Engelke, D M Markovitz

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Aptamers for Viral Detection and Inhibition.ACS infectious diseases · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Molecular recognition elements: DNA/RNA-aptamers to proteins.Biochemistry (Moscow) Supplement. Series B, Biomedical chemistry · 2010
    Review
  8. Review
  9. Article
  10. Review
  11. A nucleolar TAR decoy inhibitor of HIV-1 replication.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  12. Article
  13. In vitro correlates of HIV-2-mediated HIV-1 protection.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

C M BrowningDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan 48109, USA.
L Cagnon
P D Good
J Rossi
D R Engelke
D M Markovitz
City of Hope · USUniversity of Michigan–Ann Arbor · US

Funding

Cellular Biotechnology Training Program (CBTP)T32GM008353 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWENDEMAN, ANNA · 1991 to 2021
$9.3M
Training Program in Tumor MicroenvironmentT32CA009676 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Maria G Castro, Analisa Virginia DiFeo · 1992 to 2026
$7.3M
Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
REGULATION OF HIV2 TRANSCRIPTION BY THE PETS FACTORR01AI036685 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARKOVITZ, DAVID MICHAEL · 1994 to 2002
$929k
CHEMOKINES AND HIV REPLICATION IN ALVEOLAR MACROPHAGESR01HL057885 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COFFEY, MICHAEL J · 1996 to 2000
$305k
NCI NIH HHS T32 CA009676NHLBI NIH HHS HL-57885NIAID NIH HHS AI-36685NIGMS NIH HHS T32 GM008353NIGMS NIH HHS T32 GM-08353NIGMS NIH HHS T32 GM145304
6 · The paper itself

Abstract

Tat activation-response region (TAR) decoys have been developed for use in gene therapy for people infected with human immunodeficiency virus type 1 (HIV-1). When a TAR RNA decoy is overexpressed, it will bind Tat, thus leaving less of this crucial protein to bind to and activate the natural transcriptional promoter of HIV-1. Previous TAR decoy constructs have used HIV-1 TAR. However, recent epidemiological and biological data began to suggest that the TAR region from the human immunodeficiency virus type 2 (HIV-2) may suppress HIV-1 transcription and hence replication. We created a vector which overexpresses TAR-2 under the control of the human U6 small nuclear RNA gene promoter and here show that the U6-TAR-2 decoy construct potently inhibits both HIV-2 and HIV-1 gene expression. Further, this decoy construct is able to markedly suppress HIV-1 replication. Thus, we have directly proven that TAR-2 can suppress HIV-1 replication and suggest that the HIV-2 TAR decoy may prove useful for combating HIV-1 infection.

Indexed as

Escherichia coli ProteinsGenetic TherapyReceptors, Cell SurfaceResponse ElementsVirus ReplicationAcquired Immunodeficiency SyndromeBacterial ProteinsChemoreceptor CellsGene ExpressionGene Products, tatHIV-1HIV-2HumansMembrane ProteinsPromoter Regions, Genetictat Gene Products, Human Immunodeficiency VirusBacterial ProteinsEscherichia coli ProteinsGene Products, tatMembrane ProteinsReceptors, Cell SurfaceTar protein, E colitat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID10233987
PMCPMC112569
OpenAlexW2166447832

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.