Evidence map›Paper›PMID 10891510›Full record

ArticleMolecular and cellular biology2000

Species-specific elements in the large T-antigen J domain are required for cellular transformation and DNA replication by simian virus 40.

C S Sullivan, J D Tremblay, S W Fewell, J A Lewis, J L Brodsky, J M Pipas

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In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Copy Number Heterogeneity of JC Virus Standards.Journal of clinical microbiology · 2017
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Heat shock protein 70 (hsp70) as an emerging drug target.Journal of medicinal chemistry · 2010
    Review
  12. Article
  13. Article
  14. Multi-faceted role of HSP40 in cancer.Clinical & experimental metastasis · 2009
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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 in 1 country.

C S SullivanDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
J D Tremblay
S W Fewell
J A Lewis
J L Brodsky
J M Pipas
University of Pittsburgh · US

Funding

SV40 T ANTIGEN--ROLE IN VIRUS GROWTH AND TRANSFORMATIONR01CA040586 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PIPAS, JAMES M · 1985 to 2010
$2.7M
GENETIC ANALYSIS OF THE SV40 LARGE TUMOR ANTIGENR37CA040586 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PIPAS, JAMES M · 1988 to 1995
–
NCI NIH HHS CA40586NCI NIH HHS R01 CA040586
6 · The paper itself

Abstract

The J domain of simian virus 40 (SV40) large T antigen is required for efficient DNA replication and transformation. Despite previous reports demonstrating the promiscuity of J domains in heterologous systems, results presented here show the requirement for specific J-domain sequences in SV40 large-T-antigen-mediated activities. In particular, chimeric-T-antigen constructs in which the SV40 T-antigen J domain was replaced with that from the yeast Ydj1p or Escherichia coli DnaJ proteins failed to replicate in BSC40 cells and did not transform REF52 cells. However, T antigen containing the JC virus J domain was functional in these assays, although it was less efficient than the wild type. The inability of some large-T-antigen chimeras to promote DNA replication and elicit cellular transformation was not due to a failure to interact with hsc70, since a nonfunctional chimera, containing the DnaJ J domain, bound hsc70. However, this nonfunctional chimeric T antigen was reduced in its ability to stimulate hsc70 ATPase activity and unable to liberate E2F from p130, indicating that transcriptional activation of factors required for cell growth and DNA replication may be compromised. Our data suggest that the T-antigen J domain harbors species-specific elements required for viral activities in vivo.

Indexed as

Carrier ProteinsCell Cycle ProteinsCell Transformation, ViralDNA-Binding ProteinsDNA ReplicationProteinsVirus ReplicationAmino Acid SequenceAnimalsAntigens, Viral, TumorBacterial ProteinsBinding SitesE2F Transcription FactorsEscherichia coli ProteinsFungal ProteinsHeat-Shock ProteinsAntigens, Viral, TumorBacterial ProteinsCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsDnaJ protein, E coliE2F Transcription FactorsEscherichia coli ProteinsFungal ProteinsHeat-Shock ProteinsHSP40 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsPhosphoproteinsProteinsRecombinant ProteinsRetinoblastoma-Binding Protein 1Retinoblastoma-Like Protein p130Saccharomyces cerevisiae ProteinsTranscription Factor DP1Transcription FactorsYDJ1 protein, S cerevisiae

Identifiers

PMID10891510
PMCPMC86052
OpenAlexW2117554207

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.