Evidence map›Paper›PMID 16611888›Full record

ArticleJournal of virology2006

Targeting of p300/CREB binding protein coactivators by simian virus 40 is mediated through p53.

Darrell R Borger, James A DeCaprio

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome.Proceedings of the National Academy of Sciences of the United States of America · 2012
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  13. Identification of new p53 acetylation sites in COS-1 cells.Molecular & cellular proteomics : MCP · 2009
    Article
  14. Article
  15. Article
  16. Article
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  18. A genomic screen for activators of the antioxidant response element.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  19. Article
  20. Antagonistic pleiotropy and p53.Mechanisms of ageing and development
    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

2 authors at 1 institution in 1 country.

Darrell R BorgerDana-Farber Cancer Institute, Department of Medical Oncology, Harvard Medical School, Mayer Building 457, 44 Binney Street, Boston, Massachusetts 02115, USA.
James A DeCaprio
Dana-Farber Cancer Institute · US

Funding

RB-RELATED PROTEINS IN SV4OT AND E1A TRANSFORMATIONR01CA063113 · NCI · DANA-FARBER CANCER INSTITUTE · PI DECAPRIO, JAMES A. · 1994 to 2018
$5.0M
Role of p300/CBP in SV40 Large T Antigen TransformationF32CA099357 · NCI · DANA-FARBER CANCER INSTITUTE · PI BORGER, DARRELL R · 2004 to 2004
$49k
NCI NIH HHS F32 CA099357NCI NIH HHS F32CA99357-01A1NCI NIH HHS R01 CA063113NCI NIH HHS R01CA063113
6 · The paper itself

Abstract

The primary transforming functions of simian virus 40 large T antigen (SV40 LT) are conferred primarily through the binding and inactivation of p53 and the retinoblastoma family members. Normal p53 function requires an association with the CREB binding protein (CBP)/p300 coactivators, and a ternary complex containing SV40 LT, p53, and CBP/p300 has been identified previously. In this report, we have evaluated a secondary function of p53 bound to the SV40 LT complex in mediating the binding of human CBP/p300. We demonstrate that p53 associated with SV40 LT was posttranslationally modified in a manner consistent with the binding of CBP/p300. Furthermore, expression of SV40 LT induced the proportion of p53 phosphorylated on S15. An essential function for p53 in bridging the interaction between SV40 LT and CBP/p300 was identified through the reconstitution of the SV40 LT-CBP/p300 complex upon p53 reexpression in p53-null cells. In addition, the SV40 LT-CBP/p300 complex was disrupted through RNA interference-mediated depletion of endogenous p53. We also demonstrate that SV40 LT was acetylated in a p300- and p53-dependent manner, at least in part through the CH3 domain of p300. Therefore, the binding of p53 serves to modify SV40 LT by targeting CBP and p300 binding to direct the acetylation of SV40 LT.

Indexed as

AcetylationAnimalsAntigens, Viral, TumorCell LineCREB-Binding ProteinHumansMicePhosphorylationProtein BindingRNA, Small InterferingSimian virus 40Trans-ActivatorsTumor Suppressor Protein p53Antigens, Viral, TumorCREB-Binding ProteinRNA, Small InterferingTrans-ActivatorsTumor Suppressor Protein p53

Identifiers

PMID16611888
PMCPMC1472010
OpenAlexW2108767469

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.