Evidence map›Paper›PMID 1924346›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Isolation of a cellular protein that binds to the human immunodeficiency virus Tat protein and can potentiate transactivation of the viral promoter.

K Desai, P M Loewenstein, M Green

Erratum issuedOpen access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

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  4. Crystal structure of human p32, a doughnut-shaped acidic mitochondrial matrix protein.Proceedings of the National Academy of Sciences of the United States of America · 1999
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

K DesaiInstitute for Molecular Virology, St. Louis University School of Medicine, MO 63110.
P M Loewenstein
M Green
Washington University in St. Louis · US

Funding

REGULATION OF HIV GENE EXPRESSION BY TAT PEPTIDESR01AI028201 · NIAID · SAINT LOUIS UNIVERSITY · PI GREEN, MAURICE · 1989 to 1996
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REPLICATION OF HEPATITIS A VIRUS IN VIVOZ01AI000473 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI COHEN, J I · 1986 to 1987
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NIAID NIH HHS 5KO6 AI0473NIAID NIH HHS AI28201
6 · The paper itself

Abstract

The human immunodeficiency virus type 1 Tat protein is a powerful transactivator of the viral long terminal repeat (LTR). We have identified a cellular protein that strongly binds to Tat and can complement Tat transactivation in rodent cells. The cellular protein of about 36 kDa was isolated from extracts of human cells by Tat peptide-affinity chromatography and can form a complex with Tat in vitro. Tat transactivation is inefficient in rodent cells microinjected or transfected with the reporter plasmid pHIV-LTRCAT plus the Tat-expressing plasmid pCV-1. Remarkably, coinjection of purified 36-kDa protein with pHIV-LTRCAT plus pCV-1 stimulated Tat transactivation 2.7- to 4.9-fold. Taken together, our findings suggest that the 36-kDa protein may be a transcription factor or modulator that is important for efficient Tat transactivation.

Indexed as

HIV Long Terminal RepeatPromoter Regions, GeneticTranscriptional Activation3T3 CellsAnimalsCell LineChromatography, AffinityGene Products, tatHeLa CellsHIV-1HumansMiceMolecular WeightPlasmidsProtein BindingProteinsGene Products, tatProteinstat Gene Products, Human Immunodeficiency VirusTranscription Factors

Identifiers

PMID1924346
PMCPMC52613
OpenAlexW1997561848

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.