Evidence map›Paper›PMID 15308719›Full record

ArticleJournal of virology2004

Regulation of poliovirus 3C protease by the 2C polypeptide.

Rajeev Banerjee, Mary K Weidman, Angela Echeverri, Pallob Kundu, Asim Dasgupta

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Establishment of a panel of in-house polyclonal antibodies for the diagnosis of enterovirus infections.Neuropathology : official journal of the Japanese Society of Neuropathology · 2015
    Article
  12. Picornavirus morphogenesis.Microbiology and molecular biology reviews : MMBR · 2014
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

5 authors at 1 institution in 1 country.

Rajeev BanerjeeDepartment of Microbiology, Immunology, and Molecular Genetics, UCLA School of Medicine, University of California, Los Angeles, Los Angeles, California 90095-1747, USA.
Mary K Weidman
Angela Echeverri
Pallob Kundu
Asim Dasgupta
University of California, Los Angeles · US

Funding

INHIBITION OF HOST-CELL TRANSCRIPTION BY POLIOVIRUSR01AI027451 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DASGUPTA, ASIM · 1989 to 2003
$1.5M
NIAID NIH HHS AI27451NIAID NIH HHS R01 AI027451
6 · The paper itself

Abstract

Poliovirus-encoded nonstructural polypeptide 2C is a multifunctional protein that plays an important role in viral RNA replication. 2C interacts with both intracellular membranes and virus-specific RNAs and has ATPase and GTPase activities. Extensive computer analysis of the 2C sequence revealed that in addition to the known ATPase-, GTPase-, membrane-, and RNA-binding domains it also contains several "serpin" (serine protease inhibitor) motifs. We provide experimental evidence suggesting that 2C is indeed capable of regulating virus-encoded proteases. The purified 2C protein inhibits 3C(pro)-catalyzed cleavage of cellular transcription factors at Q-G sites in vitro. It also inhibits cleavage of a viral precursor by the other viral protease, 2A(pro). However, at least three cellular proteases appear not to be inhibited by 2C in vitro. The 2C-associated protease inhibitory activity can be depleted by anti-2C antibody. A physical interaction between 2C and His-tagged 3C(pro) can be demonstrated in vitro by coimmunoprecipitation of 2C with anti-His antibody. Deletion analysis suggests that the 2C central and C-terminal domains that include several serpin motifs are important for 3C(pro)-inhibitory activity. To examine the 2C protease inhibitory activity in vivo, stable HeLa cell lines were made that express 2C in an inducible fashion. Infection of 2C-expressing cells with poliovirus led to incomplete (or inefficient) processing of viral precursor polypeptides compared to control cell lines containing the vector alone. These results suggest that 2C can negatively regulate the viral protease 3C(pro). The possible role of the 2C protease inhibitory activity in viral RNA replication is discussed.

Indexed as

3C Viral ProteasesAmino Acid MotifsAmino Acid SequenceAntibodies, ViralCarrier ProteinsCatalysisCyclic AMP Response Element-Binding ProteinCysteine EndopeptidasesEnteropeptidaseHeLa CellsHumansMolecular Sequence DataPeptidesPoliovirusProtein BindingProtein Precursors2C protein, viral3C Viral ProteasesAntibodies, ViralCarrier ProteinsCyclic AMP Response Element-Binding ProteinCysteine EndopeptidasesEnteropeptidasePeptidespicornain 2A, PicornavirusProtein PrecursorsRNA Polymerase IIRNA, ViralSerpinsThrombinViral Nonstructural ProteinsViral Proteins

Identifiers

PMID15308719
PMCPMC506913
OpenAlexW2166677320

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.