Evidence map›Paper›PMID 23853115›Full record

ArticleThe Journal of biological chemistry2013

Interaction of E2F7 transcription factor with E2F1 and C-terminal-binding protein (CtBP) provides a mechanism for E2F7-dependent transcription repression.

Beiyu Liu, Igor Shats, Steven P Angus, Michael L Gatza, Joseph R Nevins

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

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  15. Pattern-based Search of Epigenomic Data Using GeNemo.Journal of visualized experiments : JoVE · 2017
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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

5 authors at 2 institutions in 1 country.

Beiyu LiuDuke Institute for Genome Sciences and Policy, Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27708, USA.
Igor Shats
Steven P Angus
Michael L Gatza
Joseph R Nevins
Duke University Hospital · USDuke Medical Center · US

Funding

Molecular Mechanisms of E2F SpecificityR01CA104663 · NCI · DUKE UNIVERSITY · PI NEVINS, JOSEPH R · 2003 to 2012
$3.4M
Oncogenic Gene Regulatory NetworksR01CA106520 · NCI · DUKE UNIVERSITY · PI CHI, JEN-TSAN ASHLEY · 2005 to 2014
$2.9M
NCI NIH HHS CA104663NCI NIH HHS CA106520NCI NIH HHS R01 CA104663NCI NIH HHS R01 CA106520
6 · The paper itself

Abstract

Previous work has identified distinct functions for E2F proteins during a cellular proliferative response including a role for E2F1-3 in the activation of transcription at G1/S and a role for E2F4-8 in repressing the same group of E2F1-3 target genes as cells progress through S phase. We now find that E2F7 and E2F8, which are induced by E2F1-3 at G1/S, can form a heterodimer with E2F1 through interactions involving the DNA-binding domains of the two proteins. In vitro DNA interaction assays demonstrate the formation of an E2F1-E2F7 complex, as well as an E2F7-E2F7 complex on adjacent E2F-binding sites. We also show that E2F7 recruits the co-repressor C-terminal-binding protein (CtBP) and that CtBP2 is essential for E2F7 to repress E2F1 transcription. Taken together, these findings suggest a mechanism for the repression of transcription by E2F7.

Indexed as

Alcohol OxidoreductasesCell Line, TumorCo-Repressor ProteinsE2F1 Transcription FactorE2F7 Transcription FactorG1 PhaseHEK293 CellsHumansMultiprotein ComplexesNerve Tissue ProteinsProtein MultimerizationProtein Structure, TertiaryRepressor ProteinsS PhaseTranscription, GeneticAlcohol OxidoreductasesCo-Repressor ProteinsCTBP2 protein, humanE2F1 protein, humanE2F1 Transcription FactorE2F7 protein, humanE2F7 Transcription FactorMultiprotein ComplexesNerve Tissue ProteinsRepressor ProteinsCell CycleDNA-binding ProteinE2F Transcription FactorTranscription FactorsTranscription Repressor

Identifiers

PMID23853115
PMCPMC3750156
OpenAlexW2033126852

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.