Evidence map›Paper›PMID 25883152›Full record

ArticleNucleic acids research2015

Integrative genomic analysis reveals widespread enhancer regulation by p53 in response to DNA damage.

Scott T Younger, Daniela Kenzelmann-Broz, Heiyoun Jung, Laura D Attardi, John L Rinn

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 3 pooled it
5.3field-weighted citation impact, top 4% 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

62 citing papers in PubMed, 3 syntheses or guidelines pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
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  19. Identification and characterization of functional long noncoding RNAs in cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Review
  20. Article

2 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

5 authors at 3 institutions in 1 country.

Scott T YoungerDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Daniela Kenzelmann-BrozDivision of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA.
Heiyoun JungDivision of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA.
Laura D AttardiDivision of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA.
John L RinnDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA Department of Pathology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA John_Rinn@Harvard.edu.
Stanford University · USBeth Israel Deaconess Medical Center · USBroad Institute · US

Funding

Epigenetic Regulation by Large Non-Coding RNAs in the p53 Mediated DNA Damage ResR01ES020260 · NIEHS · HARVARD UNIVERSITY · PI RINN, JOHN LOUIS · 2011 to 2015
$2.1M
NIEHS NIH HHS 1R01ES020260-01NIEHS NIH HHS R01 ES020260NIH HHS 1DP2OD00667
6 · The paper itself

Abstract

The tumor suppressor p53 has been studied extensively as a direct transcriptional activator of protein-coding genes. Recent studies, however, have shed light on novel regulatory functions of p53 within noncoding regions of the genome. Here, we use a systematic approach that integrates transcriptome-wide expression analysis, genome-wide p53 binding profiles and chromatin state maps to characterize the global regulatory roles of p53 in response to DNA damage. Notably, our approach identified conserved features of the p53 network in both human and mouse primary fibroblast models. In addition to known p53 targets, we identify many previously unappreciated mRNAs and long noncoding RNAs that are regulated by p53. Moreover, we find that p53 binding occurs predominantly within enhancers in both human and mouse model systems. The ability to modulate enhancer activity offers an additional layer of complexity to the p53 network and greatly expands the diversity of genomic elements directly regulated by p53.

Indexed as

DNA DamageEnhancer Elements, GeneticGene Expression RegulationAnimalsCell LineCells, CulturedFibroblastsGenomicsHumansMiceProteinsRNA, Long NoncodingTumor Suppressor Protein p53ProteinsRNA, Long NoncodingTumor Suppressor Protein p53

Identifiers

PMID25883152
PMCPMC4482066
OpenAlexW1980828363

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.