Evidence map›Paper›PMID 25405324›Full record

ArticleNature communications2014

CpG island-mediated global gene regulatory modes in mouse embryonic stem cells.

Samuel Beck, Bum-Kyu Lee, Catherine Rhee, Jawon Song, Andrew J Woo, Jonghwan Kim

Open access · hybridAbstract read
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Activity of PRC1 and Histone H2AK119 Monoubiquitination: Revising Popular Misconceptions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2020
    Review
  11. Article
  12. Article
  13. Chromatin folding and nuclear architecture: PRC1 function in 3D.Current opinion in genetics & development · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Intragenic CpG islands play important roles in bivalent chromatin assembly of developmental genes.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  20. Review
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 2 institutions in 2 countries.

Samuel BeckDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, Texas 78712, USA.
Bum-Kyu LeeDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, Texas 78712, USA.
Catherine RheeDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, Texas 78712, USA.
Jawon SongTexas Advanced Computing Center, The University of Texas at Austin, Austin, Texas 78758, USA.
Andrew J WooSchool of Medicine and Pharmacology, Royal Perth Hospital Unit, The University of Western Australia, Perth, WA 6000, Australia.
Jonghwan Kim1] Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas 78712, USA [2] Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, Texas 78712, USA [3] Center for Systems and Synthetic Biology, The University of Texas at Austin, Austin, Texas 78712, USA.
The University of Texas at Austin · USRoyal Perth Hospital · AU

Funding

A Myc-centered network in embryonic stem cells and somatic cell reprogrammingR00GM088384 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI KIM, JONGHWAN · 2011 to 2013
$728k
NIGMS NIH HHS R00 GM088384NIGMS NIH HHS R00GM088384
6 · The paper itself

Abstract

Both transcriptional and epigenetic regulations are fundamental for the control of eukaryotic gene expression. Here we perform a compendium analysis of >200 large sequencing data sets to elucidate the regulatory logic of global gene expression programs in mouse embryonic stem (ES) cells. We define four major classes of DNA-binding proteins (Core, PRC, MYC and CTCF) based on their target co-occupancy, and discover reciprocal regulation between the MYC and PRC classes for the activity of nearly all genes under the control of the CpG island (CGI)-containing promoters. This CGI-dependent regulatory mode explains the functional segregation between CGI-containing and CGI-less genes during early development. By defining active enhancers based on the co-occupancy of the Core class, we further demonstrate their additive roles in CGI-containing gene expression and cell type-specific roles in CGI-less gene expression. Altogether, our analyses provide novel insights into previously unknown CGI-dependent global gene regulatory modes.

Indexed as

AnimalsBase SequenceCell LineCpG IslandsDNA-Binding ProteinsDNA MethylationEmbryonic Stem CellsEnhancer Elements, GeneticGene Expression RegulationGenes, RegulatorMicePolycomb-Group ProteinsPromoter Regions, GeneticProto-Oncogene Proteins c-mycSequence Analysis, DNADNA-Binding ProteinsMyc protein, mousePolycomb-Group ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID25405324
PMCPMC4236720
OpenAlexW1982323384

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.