Evidence map›Paper›PMID 9371601›Full record

ArticleJournal of virology1997

The DnaJ domain of polyomavirus large T antigen is required to regulate Rb family tumor suppressor function.

Q Sheng, D Denis, M Ratnofsky, T M Roberts, J A DeCaprio, B Schaffhausen

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 88 citations in OpenAlex.

  1. Review
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  11. Lessons in signaling and tumorigenesis from polyomavirus middle T antigen.Microbiology and molecular biology reviews : MMBR · 2009
    Review
  12. Review
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  15. Article
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  19. Article
  20. T' proteins influence JC virus biology.Journal of neurovirology · 2003
    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.

Q ShengDepartment of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
D Denis
M Ratnofsky
T M Roberts
J A DeCaprio
B Schaffhausen
Tufts University · US

Funding

VIRAL ONCOPROTEIN PERTURBATION OF RB/E2F PATHWAYP01CA050661 · NCI · DANA-FARBER CANCER INSTITUTE · PI HOWLEY, PETER M · 1989 to 2013
$35.8M
PRODUCTS OF THE TRANSFORMING GENES OF POLYOMAVIRUSR01CA034722 · NCI · TUFTS UNIVERSITY BOSTON · PI SCHAFFHAUSEN, BRIAN S · 1985 to 2015
$6.0M
PRODUCTS OF THE TRANSFORMING GENES OF POLYOMA VIRUSR37CA034722 · NCI · TUFTS UNIVERSITY BOSTON · PI SCHAFFHAUSEN, BRIAN S · 1991 to 1998
–
NCI NIH HHS CA32222NCI NIH HHS CA34722NCI NIH HHS CA50661NCI NIH HHS R01 CA034722
6 · The paper itself

Abstract

Tumor suppressors of the retinoblastoma susceptibility gene family regulate cell growth and differentiation. Polyomavirus large T antigens (large T) bind Rb family members and block their function. Mutations of large T sequences conserved with the DnaJ family affect large T binding to a cellular DnaK, heat shock protein 70. The same mutations abolish large T activation of E2F-containing promoters and Rb binding-dependent large T activation of cell cycle progression. Cotransfection of a cellular DnaJ domain blocks wild-type large T action, showing that the connection between the chaperone system and tumor suppressors is direct. Although they are inactive in assays dependent on Rb family binding, mutants in the J region retain the ability to associate with pRb, p107, and p130. This suggests that binding of Rb family members by large T is not sufficient for their inactivation and that a functional J domain is required as well. This work connects the DnaJ and DnaK molecular chaperones to regulation of tumor suppressors by polyomavirus large T.

Indexed as

Carrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsProteins3T3 CellsAmino Acid SequenceAnimalsAntigens, Polyomavirus TransformingBinding SitesE2F Transcription FactorsHeat-Shock ProteinsHSP40 Heat-Shock ProteinsHumansMiceMolecular Sequence DataMutagenesisAntigens, Polyomavirus TransformingArid4a protein, mouseCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsE2F Transcription FactorsHeat-Shock ProteinsHSP40 Heat-Shock ProteinsNuclear ProteinsPhosphoproteinsProteinsRBL1 protein, humanRbl1 protein, mouseRBL2 protein, humanRbl2 protein, mouseRepressor ProteinsRetinoblastoma-Binding Protein 1Retinoblastoma-Like Protein p107Retinoblastoma-Like Protein p130Retinoblastoma ProteinTranscription Factor DP1Transcription Factors

Identifiers

PMID9371601
PMCPMC230245
OpenAlexW1533683254

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.