Evidence map›Paper›PMID 25215497›Full record

ArticleCell2014

Determination and inference of eukaryotic transcription factor sequence specificity.

Matthew T Weirauch, Ally Yang, Mihai Albu, Atina G Cote, Alejandro Montenegro-Montero, Philipp Drewe, Hamed S Najafabadi, Samuel A Lambert, Ishminder Mann, Kate Cook and 18 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,190 papers.

0numbers the graph read from it
0cells of the map it votes in
1,190citing papers in PubMed
43.4field-weighted citation impact, top 1% 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

1,190 citing papers in PubMed, 2,002 citations in OpenAlex.

  1. Inferring Gene Regulatory Networks in Stem Cells: Methods and Applications.Methods in molecular biology (Clifton, N.J.) · 2027
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. UnlockingNAR genomics and bioinformatics · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

1,130 more citing papers are in PubMed but not listed here.

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

28 authors at 10 institutions in 4 countries.

Matthew T WeirauchCenter for Autoimmune Genomics and Etiology (CAGE) and Divisions of Biomedical Informatics and Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA; Banting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Ally YangBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Mihai AlbuBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Atina G CoteBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Alejandro Montenegro-MonteroDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Philipp DreweComputational Biology Center, Sloan-Kettering Institute, New York, NY 10065, USA.
Hamed S NajafabadiBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Samuel A LambertDepartment of Molecular Genetics, University of Toronto, Toronto ON M5S 1A8, Canada.
Ishminder MannBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Kate CookDepartment of Molecular Genetics, University of Toronto, Toronto ON M5S 1A8, Canada.
Hong ZhengBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada.
Alejandra GoityDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Harm van BakelBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada; Icahn Institute for Genomics and Multiscale Biology, Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY 10029, USA.
Jean-Claude LozanoSorbonne Universités, UPMC Univ Paris 06, CNRS UMR 7621, CNRS, Laboratoire d'Océanographie Microbienne, Observatoire Océanologique, F-66650 Banyuls/mer, France.
Mary GalliGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Mathew G LewseyGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Eryong HuangDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Tuhin MukherjeeDepartment of Electronic and Computing Systems, University of Cincinnati, Cincinnati, OH 45221, USA.
Xiaoting ChenDepartment of Electronic and Computing Systems, University of Cincinnati, Cincinnati, OH 45221, USA.
John S Reece-HoyesProgram in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Sridhar GovindarajanDNA2.0 Inc., Menlo Park, CA 94025, USA.
Gad ShaulskyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Albertha J M WalhoutProgram in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
François-Yves BougetSorbonne Universités, UPMC Univ Paris 06, CNRS UMR 7621, CNRS, Laboratoire d'Océanographie Microbienne, Observatoire Océanologique, F-66650 Banyuls/mer, France.
Gunnar RatschComputational Biology Center, Sloan-Kettering Institute, New York, NY 10065, USA.
Luis F LarrondoDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago 8331150, Chile.
Joseph R EckerGenomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Plant Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Timothy R HughesBanting and Best Department of Medical Research and Donnelly Centre, University of Toronto, Toronto ON M5S 3E1, Canada; Department of Molecular Genetics, University of Toronto, Toronto ON M5S 1A8, Canada. Electronic address: t.hughes@utoronto.ca.
University of Toronto · CAPontificia Universidad Católica de Chile · CLSalk Institute for Biological Studies · USBaylor College of Medicine · USKettering University · USUniversity of Cincinnati · USUniversity of Massachusetts Chan Medical School · USCentre National de la Recherche Scientifique · FRMenlo School · USSorbonne Université · FR

Funding

PROJECT III - Computational Analysis of Phenotypes andP01HD039691 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI SUCGANG, RICHARD · 2001 to 2016
$14.4M
Identifying transcription factor binding sites in the C. elegans genomeR01GM082971 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WALHOUT, A. J. MARIAN · 2008 to 2016
$5.8M
CIHR MOP-77721Howard Hughes Medical InstituteNICHD NIH HHS P01 HD039691NICHD NIH HHS P01 HD39691NIGMS NIH HHS GM082971NIGMS NIH HHS R01 GM082971
6 · The paper itself

Abstract

Transcription factor (TF) DNA sequence preferences direct their regulatory activity, but are currently known for only ∼1% of eukaryotic TFs. Broadly sampling DNA-binding domain (DBD) types from multiple eukaryotic clades, we determined DNA sequence preferences for >1,000 TFs encompassing 54 different DBD classes from 131 diverse eukaryotes. We find that closely related DBDs almost always have very similar DNA sequence preferences, enabling inference of motifs for ∼34% of the ∼170,000 known or predicted eukaryotic TFs. Sequences matching both measured and inferred motifs are enriched in chromatin immunoprecipitation sequencing (ChIP-seq) peaks and upstream of transcription start sites in diverse eukaryotic lineages. SNPs defining expression quantitative trait loci in Arabidopsis promoters are also enriched for predicted TF binding sites. Importantly, our motif "library" can be used to identify specific TFs whose binding may be altered by human disease risk alleles. These data present a powerful resource for mapping transcriptional networks across eukaryotes.

Indexed as

Nucleotide MotifsSequence Analysis, DNAArabidopsisChromatin ImmunoprecipitationHumansPolymorphism, Single NucleotidePromoter Regions, GeneticProtein BindingQuantitative Trait LociTranscription FactorsTranscription Factors

Identifiers

PMID25215497
PMCPMC4163041
OpenAlexW2033169664

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.