Evidence map›Paper›PMID 12857933›Full record

ArticleJournal of virology2003

A naturally occurring substitution in human immunodeficiency virus Tat increases expression of the viral genome.

Syed M Reza, Lin-Ming Shen, Rupa Mukhopadhyay, Mihaela Rosetti, Tsafi Pe'ery, Michael B Mathews

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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 1 institution.

Syed M RezaDepartment of Biochemistry and Molecular Biology, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, New Jersey 01701, USA.
Lin-Ming Shen
Rupa Mukhopadhyay
Mihaela Rosetti
Tsafi Pe'ery
Michael B Mathews
Rutgers New Jersey Medical School

Funding

REGULATION OF HIV1 GENE EXPRESSION BY TAT AND TARR01AI031802 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI MATHEWS, MICHAEL B · 1992 to 2001
$642k
NIAID NIH HHS AI31802
6 · The paper itself

Abstract

A natural amino acid substitution in the human immunodeficiency virus type 1 (HIV-1) transcriptional activator Tat increases its activity and compensates for deleterious mutations elsewhere in the Tat protein. Substitution of asparagine for threonine 23 increases Tat transactivation of the HIV-1 promoter and the binding of Tat to the cellular kinase positive transcription elongation factor b (P-TEFb). Of nine other position 23 mutations tested, only the serine substitution retained wild-type activity. Correspondingly, asparagine is the most frequent amino acid at this position in HIV-1 isolates, followed by threonine and serine. Asparagine is prevalent in Tat proteins of viruses in clades A, C, and D, which are major etiologic agents of AIDS. We suggest that selection for asparagine in position 23 confers an advantage to the virus, since it can compensate for deleterious mutations in Tat. It may also support the replication of otherwise less fit drug-resistant viruses and permit the emergence of virulent strains.

Indexed as

Amino Acid SubstitutionGenome, ViralTranscription, GeneticAmino Acid SequenceAsparagineGene Products, tatGenetic VariationHIV-1HumansLeukocytes, MononuclearMolecular Sequence DataPositive Transcriptional Elongation Factor BProtein Serine-Threonine Kinasestat Gene Products, Human Immunodeficiency VirusTranscriptional ActivationAsparagineGene Products, tatPositive Transcriptional Elongation Factor BProtein Serine-Threonine Kinasestat Gene Products, Human Immunodeficiency Virus

Identifiers

PMID12857933
PMCPMC165250
OpenAlexW2161990493

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.