Evidence map›Paper›PMID 27899590›Full record

ArticleNucleic acids research2017

Different enhancer classes in Drosophila bind distinct architectural proteins and mediate unique chromatin interactions and 3D architecture.

Caelin Cubeñas-Potts, M Jordan Rowley, Xiaowen Lyu, Ge Li, Elissa P Lei, Victor G Corces

Abstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing 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

95 citing papers in PubMed.

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  12. ThebioRxiv : the preprint server for biology · 2025
    Article
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  17. Mechanistic drivers of chromatin organization into compartments.Current opinion in genetics & development · 2024
    Review
  18. Science advances · 2024
    Article
  19. Article
  20. Article

35 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

6 authors.

Caelin Cubeñas-PottsDepartment of Biology, Emory University, 1510 Clifton Rd NE, Atlanta, GA 30322, USA.
M Jordan RowleyDepartment of Biology, Emory University, 1510 Clifton Rd NE, Atlanta, GA 30322, USA.
Xiaowen LyuDepartment of Biology, Emory University, 1510 Clifton Rd NE, Atlanta, GA 30322, USA.
Ge LiDepartment of Biology, Emory University, 1510 Clifton Rd NE, Atlanta, GA 30322, USA.
Elissa P LeiNuclear Organization and Gene Expression Section, Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA.
Victor G CorcesDepartment of Biology, Emory University, 1510 Clifton Rd NE, Atlanta, GA 30322, USA.

Funding

Chromatin Insulator Function and Nuclear OrganizationZIADK015602 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LEI, ELISSA · 2009 to 2025
$24.7M
MOLECULAR BASIS OF SUPPRESSION IN DROSOPHILAR01GM035463 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORCES, VICTOR G. · 1986 to 2020
$10.7M
Control of chromatin organization by nucleosome remodelers and long non-coding RNAF32GM113570 · NIGMS · EMORY UNIVERSITY · PI ROWLEY, MICHAEL JORDAN · 2015 to 2017
$162k
NIGMS NIH HHS F32 GM113570NIGMS NIH HHS R01 GM035463
6 · The paper itself

Abstract

Eukaryotic gene expression is regulated by enhancer-promoter interactions but the molecular mechanisms that govern specificity have remained elusive. Genome-wide studies utilizing STARR-seq identified two enhancer classes in Drosophila that interact with different core promoters: housekeeping enhancers (hkCP) and developmental enhancers (dCP). We hypothesized that the two enhancer classes are occupied by distinct architectural proteins, affecting their enhancer-promoter contacts. By evaluating ChIP-seq occupancy of architectural proteins, typical enhancer-associated proteins, and histone modifications, we determine that both enhancer classes are enriched for RNA Polymerase II, CBP, and architectural proteins but there are also distinctions. hkCP enhancers contain H3K4me3 and exclusively bind Cap-H2, Chromator, DREF and Z4, whereas dCP enhancers contain H3K4me1 and are more enriched for Rad21 and Fs(1)h-L. Additionally, we map the interactions of each enhancer class utilizing a Hi-C dataset with <1 kb resolution. Results suggest that hkCP enhancers are more likely to form multi-TSS interaction networks and be associated with topologically associating domain (TAD) borders, while dCP enhancers are more often bound to one or two TSSs and are enriched at chromatin loop anchors. The data support a model suggesting that the unique architectural protein occupancy within enhancers is one contributor to enhancer-promoter interaction specificity.

Indexed as

DNA-Binding ProteinsEnhancer Elements, GeneticAnimalsBiomarkersCell LineChromatinChromatin ImmunoprecipitationComputational BiologyDrosophilaHigh-Throughput Nucleotide SequencingHistonesPromoter Regions, GeneticProtein BindingBiomarkersChromatinDNA-Binding ProteinsHistones

Identifiers

PMID27899590
PMCPMC5389536

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.