Evidence map›Paper›PMID 22404213›Full record

ArticleAIDS research and human retroviruses2012

Identification of cellular proteins required for replication of human immunodeficiency virus type 1.

Natallia Dziuba, Monique R Ferguson, William A O'Brien, Anthony Sanchez, Andrew J Prussia, Natalie J McDonald, Brian M Friedrich, Guangyu Li, Michael W Shaw, Jinsong Sheng and 3 more

Abstract read
In one paragraph

Article in AIDS research and human retroviruses, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 21% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. DNAJA: emerging targets for anti-tumor therapy.Future oncology (London, England) · 2025
    Review
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  5. Article
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  16. Review
  17. Broad-spectrum antiviral agents.Frontiers in microbiology · 2015
    Review
  18. Article
  19. Article
  20. 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

13 authors at 4 institutions in 1 country.

Natallia DziubaDepartment of Internal Medicine, University of Texas Medical Branch, Galveston, USA.
Monique R Ferguson
William A O'Brien
Anthony Sanchez
Andrew J Prussia
Natalie J McDonald
Brian M Friedrich
Guangyu Li
Michael W Shaw
Jinsong Sheng
Thomas W Hodge
Donald H Rubin
James L Murray
The University of Texas Medical Branch at Galveston · USCenters for Disease Control and Prevention · USVanderbilt University · USEmory University · US

Funding

Role of Tetraspan Glycoproteins (CD63) in HIV ReplicationR01HL088999 · NHLBI · UNIVERSITY OF TEXAS MED BR GALVESTON · PI FERGUSON, MONIQUE REGAIL · 2006 to 2011
$2.5M
Characterization of Cellular Proteins Involved in HIV InfectionR43AI084705 · NIAID · ZIRUS, INC. · PI O'BRIEN, WILLIAM AUSTIN · 2009 to 2009
$431k
NHLBI NIH HHS HL088999NIAID NIH HHS AI084705
6 · The paper itself

Abstract

Cellular proteins are essential for human immunodeficiency virus type 1 (HIV-1) replication and may serve as viable new targets for treating infection. Using gene trap insertional mutagenesis, a high-throughput approach based on random inactivation of cellular genes, candidate genes were found that limit virus replication when mutated. Disrupted genes (N=87) conferring resistance to lytic infection with several viruses were queried for an affect on HIV-1 replication by utilizing small interfering RNA (siRNA) screens in TZM-bl cells. Several genes regulating diverse pathways were found to be required for HIV-1 replication, including DHX8, DNAJA1, GTF2E1, GTF2E2, HAP1, KALRN, UBA3, UBE2E3, and VMP1. Candidate genes were independently tested in primary human macrophages, toxicity assays, and/or Tat-dependent β-galactosidase reporter assays. Bioinformatics analyses indicated that several host factors present in this study participate in canonical pathways and functional processes implicated in prior genome-wide studies. However, the genes presented in this study did not share identity with those found previously. Novel antiviral targets identified in this study should open new avenues for mechanistic investigation.

Indexed as

Cell LineCells, CulturedFemaleGene Expression RegulationHIV-1HumansMaleMass ScreeningMutagenesis, InsertionalRNA, MessengerRNA, Small InterferingRNA, ViralVirus ActivationVirus ReplicationRNA, MessengerRNA, Small InterferingRNA, Viral

Identifiers

PMID22404213
PMCPMC3448097
OpenAlexW1998276064

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.