Evidence map›Paper›PMID 22898364›Full record

ArticleMethods (San Diego, Calif.)2012

Comparative analysis of virus-host interactomes with a mammalian high-throughput protein complementation assay based on Gaussia princeps luciferase.

Grégory Neveu, Patricia Cassonnet, Pierre-Olivier Vidalain, Caroline Rolloy, José Mendoza, Louis Jones, Frédéric Tangy, Mandy Muller, Caroline Demeret, Lionel Tafforeau and 8 more

Abstract readComparative Study
In one paragraph

Article in Methods (San Diego, Calif.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Protein-protein interactions of human viruses.Seminars in cell & developmental biology · 2020
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. System pharmacogenomics application in infectious diseases.Briefings in functional genomics · 2017
    Review
  19. The Promise of Proteomics in the Study of Oncogenic Viruses.Molecular & cellular proteomics : MCP · 2017
    Review
  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

18 authors.

Grégory NeveuUnité de Génétique, Papillomavirus et Cancer Humain (GPCH), Institut Pasteur, Paris, France.
Patricia Cassonnet
Pierre-Olivier Vidalain
Caroline Rolloy
José Mendoza
Louis Jones
Frédéric Tangy
Mandy Muller
Caroline Demeret
Lionel Tafforeau
Vincent Lotteau
Chantal Rabourdin-Combe
Gilles Travé
Amélie Dricot
David E Hill
Marc Vidal
Michel Favre
Yves Jacob

Funding

Genomic Analysis of Network Perturbations in Human DiseaseP50HG004233 · NHGRI · DANA-FARBER CANCER INST · PI VIDAL, MARC · 2007 to 2017
$31.6M
NHGRI NIH HHS P50 HG004233NHGRI NIH HHS P50-HG004233PHS HHS R01-H6001715
6 · The paper itself

Abstract

Comparative interactomics is a strategy for inferring potential interactions among orthologous proteins or "interologs". Herein we focus, in contrast to standard homology-based inference, on the divergence of protein interaction profiles among closely related organisms, showing that the approach can correlate specific traits to phenotypic differences. As a model, this new comparative interactomic approach was applied at a large scale to human papillomaviruses (HPVs) proteins. The oncogenic potential of HPVs is mainly determined by the E6 and E7 early proteins. We have mapped and overlapped the virus-host protein interaction networks of E6 and E7 proteins from 11 distinct HPV genotypes, selected for their different tropisms and pathologies. We generated robust and comprehensive datasets by combining two orthogonal protein interaction assays: yeast two-hybrid (Y2H), and our recently described "high-throughput Gaussia princeps protein complementation assay" (HT-GPCA). HT-GPCA detects protein interaction by measuring the interaction-mediated reconstitution of activity of a split G. princeps luciferase. Hierarchical clustering of interaction profiles recapitulated HPV phylogeny and was used to correlate specific virus-host interaction profiles with pathological traits, reflecting the distinct carcinogenic potentials of different HPVs. This comparative interactomics constitutes a reliable and powerful strategy to decipher molecular relationships in virtually any combination of microorganism-host interactions.

Indexed as

Host-Pathogen InteractionsTwo-Hybrid System TechniquesAlphapapillomavirusArecaceaeBiomarkersCluster AnalysisGenotypeHEK293 CellsHumansLuciferasesOncogene Proteins, ViralPapillomavirus E7 ProteinsPhylogenyPlant ProteinsProtein BindingProtein Interaction MappingBiomarkersE6 protein, Human papillomavirus type 16LuciferasesOncogene Proteins, ViralPapillomavirus E7 ProteinsPlant ProteinsProteomeRecombinant Fusion ProteinsRepressor Proteins

Identifiers

PMID22898364
PMCPMC3546263

What OpenQuestion holds

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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.