Evidence map›Paper›PMID 27421669›Full record

ReviewGene2016

An evolutionary, structural and functional overview of the mammalian TEAD1 and TEAD2 transcription factors.

André Landin-Malt, Ataaillah Benhaddou, Alain Zider, Domenico Flagiello

Open access · greenAbstract readReview
In one paragraph

Review in Gene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  8. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate.International journal of molecular sciences · 2024
    Review
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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 3 institutions in 2 countries.

André Landin-MaltDepartment of Cell Biology, University of Virginia Health System, Charlottesville, VA 22908, USA. Electronic address: alandinmalt@virginia.edu.
Ataaillah BenhaddouUniv Paris Diderot, Sorbonne Paris Cité, Team Regulation of Cell-Fate Specification in the Mouse, IJM, UMR 7592 CNRS, Paris, France. Electronic address: ataaillah.benhaddou@ijm.fr.
Alain ZiderUniv Paris Diderot, Sorbonne Paris Cité, Team Molecular Oncology and Ovarian Pathologies, IJM, UMR 7592 CNRS, Paris, France. Electronic address: alain.zider@ijm.fr.
Domenico FlagielloUniv Paris Diderot, Sorbonne Paris Cité, Team Regulation of Cell-Fate Specification in the Mouse, IJM, UMR 7592 CNRS, Paris, France. Electronic address: domenico.flagiello@ijm.fr.
Sorbonne Paris Cité · FRUniversité Paris Cité · FRUniversity of Virginia · US

Funding

The Gene Wiki: Community intelligence applied to gene annotationR01GM089820 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SU, ANDREW I · 2010 to 2021
$5.2M
NIGMS NIH HHS R01 GM089820
6 · The paper itself

Abstract

TEAD proteins constitute a family of highly conserved transcription factors, characterized by a DNA-binding domain called the TEA domain and a protein-binding domain that permits association with transcriptional co-activators. TEAD proteins are unable to induce transcription on their own. They have to interact with transcriptional cofactors to do so. Once TEADs bind their co-activators, the different complexes formed are known to regulate the expression of genes that are crucial for embryonic development, important for organ formation (heart, muscles), and involved in cell death and proliferation. In the first part of this review we describe what is known of the structure of TEAD proteins. We then focus on two members of the family: TEAD1 and TEAD2. First the different transcriptional cofactors are described. These proteins can be classified in three categories: i), cofactors regulating chromatin conformation, ii), cofactors able to bind DNA, and iii), transcriptional cofactors without DNA binding domain. Finally we discuss the recent findings that identified TEAD1 and 2 and its coactivators involved in cancer progression.

Indexed as

Evolution, MolecularAnimalsDNA-Binding ProteinsHumansMammalsTranscription FactorsDNA-Binding ProteinsTranscription FactorsCancerTEATEADTranscription factorVGLLYAP

Identifiers

PMID27421669
PMCPMC7034536
OpenAlexW2467240885

What OpenQuestion holds

Textmetadata
LicenceTDM
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.