Evidence map›Paper›PMID 20448036›Full record

ArticleThe Journal of biological chemistry2010

Transcriptional synergy between melanoma antigen gene protein-A11 (MAGE-11) and p300 in androgen receptor signaling.

Emily B Askew, Suxia Bai, Amanda J Blackwelder, Elizabeth M Wilson

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. The Ser434PheThe application of clinical genetics · 2024
    Article
  4. Diagnostics (Basel, Switzerland) · 2022
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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

4 authors at 1 institution in 3 countries.

Emily B AskewDepartment of Pediatrics, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
Suxia Bai
Amanda J Blackwelder
Elizabeth M Wilson
University of North Carolina at Chapel Hill · US

Funding

Tumor stem cells in androgen independent prostate cancerP01CA077739 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRENCH, FRANK S, MOHLER, JAMES L · 1998 to 2014
$16.8M
TESTIS SPECIFIC HISTONE BINDING PROTEIN (NASP)U54HD035041 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PETRUSZ, PETER · 1997 to 2011
$16.1M
ANDROGEN RECEPTOR REGULATION OF REPRODUCTIVE FUNCTIONR01HD016910 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WILSON, ELIZABETH M. · 1985 to 2010
$2.8M
ANDROGEN RECEPTOR REGULATION OF REPRODUCTIVE FUNCTIONR37HD016910 · NICHD · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI WILSON, ELIZABETH M. · 1993 to 2002
$1.1M
Howard Hughes Medical InstituteNCI NIH HHS CA77739NCI NIH HHS P01 CA077739NCI NIH HHS PC073586NICHD NIH HHS HD16910NICHD NIH HHS R01 HD016910NICHD NIH HHS R37 HD016910NICHD NIH HHS U54 HD035041NICHD NIH HHS U54-HD35041
6 · The paper itself

Abstract

Androgen receptor (AR)-mediated gene regulation involves interactions with coregulatory proteins that include the melanoma antigen gene protein-A11 (MAGE-11). To understand the functional significance of sequence similarity between MAGE-11 and the adenovirus early protein E1A, we determined whether MAGE-11 contributes to AR transcriptional activity through an interaction with p300, a potent and ubiquitous transcriptional regulator. Here, we report that MAGE-11 interacts with the NH(2)-terminal region of p300 through the MAGE-11 MXXIF motif (185)MXXIF(189), with transcriptional activity depending on the MAGE-11 F-box and MAPK phosphorylation. The MAGE-11- and p300-dependent increase in AR transactivation required the NH(2)-terminal regions of AR and p300, p300 acetyltransferase activity, and the AR FXXLF motif (23)FQNLF(27) interaction with MAGE-11. MAGE-11 linked AR to p300 and the p160 coactivator, transcriptional intermediary protein 2 (TIF2). The p300 NH(2)-terminal FXXLF motif (33)FGSLF(37) was required for transcriptional activation by TIF2. Increased expression of p300 decreased the ubiquitinylation of MAGE-11 and transiently increased endogenous MAGE-11 levels. Autoacetylation of p300 and decreased acetylation of TIF2 were evident in the MAGE-11, p300, and TIF2 complex. The studies suggest that MAGE-11 links NH(2)-terminal domains of AR and p300 to promote transcriptional synergy through a cadre of FXXLF-related interacting motifs.

Indexed as

Amino Acid MotifsAndrogensAnimalsAntigens, NeoplasmChlorocebus aethiopsCOS CellsE1A-Associated p300 ProteinHeLa CellsHumansModels, BiologicalNeoplasm ProteinsPhosphorylationReceptors, AndrogenReceptors, Cytoplasmic and NuclearReceptors, SteroidTranscription, GeneticAndrogensAntigens, NeoplasmE1A-Associated p300 ProteinEP300 protein, humanMAGEA11 protein, humanNeoplasm ProteinsReceptors, AndrogenReceptors, Cytoplasmic and NuclearReceptors, Steroid

Identifiers

PMID20448036
PMCPMC2898404
OpenAlexW2077044630

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.