Evidence map›Paper›PMID 26185160›Full record

ArticleG3 (Bethesda, Md.)2015

GABPα Binding to Overlapping ETS and CRE DNA Motifs Is Enhanced by CREB1: Custom DNA Microarrays.

Ximiao He, Khund Sayeed Syed, Desiree Tillo, Ishminder Mann, Matthew T Weirauch, Charles Vinson

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

6 authors at 3 institutions in 1 country.

Ximiao HeLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.ORCID http://orcid.org/0000-0003-1253-5275
Khund Sayeed SyedLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Desiree TilloLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Ishminder MannLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Matthew T WeirauchCenter for Autoimmune Genomics and Etiology, Division of Biomedical Informatics and Division of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229 matthew.weirauch@cchmc.org vinsonc@mail.nih.gov.
Charles VinsonLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892 matthew.weirauch@cchmc.org vinsonc@mail.nih.gov.
National Cancer Institute · USNational Institutes of Health · USCincinnati Children's Hospital Medical Center · US

Funding

Gene Regulation and Function: The B-ZIP ProteinsZIABC005271 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI VINSON, CHARLES · 2009 to 2019
$11.2M
6 · The paper itself

Abstract

To achieve proper spatiotemporal control of gene expression, transcription factors cooperatively assemble onto specific DNA sequences. The ETS domain protein monomer of GABPα and the B-ZIP domain protein dimer of CREB1 cooperatively bind DNA only when the ETS ((C)/GCGGAA GT: ) and CRE ( GT: GACGTCAC) motifs overlap precisely, producing the ETS↔CRE motif ((C)/GCGGAA GT: GACGTCAC). We designed a Protein Binding Microarray (PBM) with 60-bp DNAs containing four identical sectors, each with 177,440 features that explore the cooperative interactions between GABPα and CREB1 upon binding the ETS↔CRE motif. The DNA sequences include all 15-mers of the form (C)/GCGGA--CG-, the ETS↔CRE motif, and all single nucleotide polymorphisms (SNPs), and occurrences in the human and mouse genomes. CREB1 enhanced GABPα binding to the canonical ETS↔CRE motif CCGGAAGT two-fold, and up to 23-fold for several SNPs at the beginning and end of the ETS motif, which is suggestive of two separate and distinct allosteric mechanisms of cooperative binding. We show that the ETS-CRE array data can be used to identify regions likely cooperatively bound by GABPα and CREB1 in vivo, and demonstrate their ability to identify human genetic variants that might inhibit cooperative binding.

Indexed as

Binding SitesNucleotide MotifsAnimalsCell LineCyclic AMP Response Element-Binding ProteinGA-Binding Protein Transcription FactorGenetic LociHumansMiceOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideProtein BindingProto-Oncogene Proteins c-etsRecombinant Fusion ProteinsCyclic AMP Response Element-Binding ProteinGA-Binding Protein Transcription FactorProto-Oncogene Proteins c-etsRecombinant Fusion Proteinscooperative DNA bindingCRECREB1ETSGABPα

Identifiers

PMID26185160
PMCPMC4555227
OpenAlexW2336460587

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.