Evidence map›Paper›PMID 27634217›Full record

ArticleNature communications2016

Capture of associated targets on chromatin links long-distance chromatin looping to transcriptional coordination.

Ryan J Bourgo, Hari Singhal, Geoffrey L Greene

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

3 authors.

Ryan J BourgoBen May Department of Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.
Hari SinghalBen May Department of Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.
Geoffrey L GreeneBen May Department of Cancer Research, University of Chicago, Chicago, Illinois 60637, USA.

Funding

Development and Characterization of Novel SERMsR01CA089489 · NCI · UNIVERSITY OF CHICAGO · PI GREENE, GEOFFREY L · 2001 to 2011
$4.3M
NCI NIH HHS R01 CA089489
6 · The paper itself

Abstract

Here we describe a sensitive and novel method of identifying endogenous DNA-DNA interactions. Capture of Associated Targets on CHromatin (CATCH) uses efficient capture and enrichment of specific genomic loci of interest through hybridization and subsequent purification via complementary biotinylated oligonucleotide. The CATCH assay requires no enzymatic digestion or ligation, requires little starting material, provides high-quality data, has excellent reproducibility and is completed in less than 24 h. Efficacy is demonstrated through capture of three disparate loci, which demonstrate unique subsets of long-distance chromatin interactions enriched for both enhancer marks and oestrogen receptor-binding sites. In each experiment, CATCH-seq peaks representing long-distance chromatin interactions were centred near the TSS of genes, and, critically, the genes identified as physically interacting are shown to be transcriptionally coexpressed. These interactions could potentially create transcriptional hubs for the regulation of gene expression programmes.

Indexed as

ChromatinBinding SitesChromatin ImmunoprecipitationDNAEndoplasmic ReticulumEukaryotic Initiation Factor-4AGene Expression RegulationGenomicsHumansPromoter Regions, GeneticProtein BindingSequence Analysis, DNAChromatinDNAEukaryotic Initiation Factor-4A

Identifiers

PMID27634217
PMCPMC5028417

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.