Evidence map›Paper›PMID 28628087›Full record

ArticleNature structural & molecular biology2017

Chromatin-enriched lncRNAs can act as cell-type specific activators of proximal gene transcription.

Michael S Werner, Matthew A Sullivan, Rohan N Shah, Rangarajan D Nadadur, Adrian T Grzybowski, Vasiliy Galat, Ivan P Moskowitz, Alexander J Ruthenburg

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

58 citing papers in PubMed, 100 citations in OpenAlex.

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  17. Emerging Functions of lncRNA Loci beyond the Transcript Itself.International journal of molecular sciences · 2022
    Review
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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

8 authors at 2 institutions in 1 country.

Michael S WernerDepartment of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA.
Matthew A SullivanDepartment of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA.
Rohan N ShahDepartment of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA.
Rangarajan D NadadurDepartment of Pediatrics and Pathology, The University of Chicago, Chicago, Illinois, USA.
Adrian T GrzybowskiDepartment of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA.
Vasiliy GalatDepartment of Pathology, Stanley Manne Children's Research Institute, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Ivan P MoskowitzDepartment of Pediatrics and Pathology, The University of Chicago, Chicago, Illinois, USA.
Alexander J RuthenburgDepartment of Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois, USA.ORCID http://orcid.org/0000-0003-2709-4564
University of Chicago · USNorthwestern University · US

Funding

MULTIDISCIPLINARY CARDIAC SCIENCEST32HL007381 · NHLBI · UNIVERSITY OF CHICAGO · PI JEANNE M DECARA, Yoav Gilad · 1985 to 2026
$12.5M
Quantitatively probing intra-nucleosomal chromatin variation and functionR01GM115945 · NIGMS · UNIVERSITY OF CHICAGO · PI RUTHENBURG, ALEXANDER JACKSON · 2016 to 2020
$1.6M
NHLBI NIH HHS T32 HL007381NIGMS NIH HHS R01 GM115945
6 · The paper itself

Abstract

We recently described a new class of long noncoding RNAs (lncRNAs) that are distinguished by especially tight chromatin association and whose presence is strongly correlated to expression of nearby genes. Here, we examine the cis-enhancer mechanism of this class of chromatin-enriched RNA (cheRNA) across multiple human cell lines. cheRNAs are largely cell type specific and provide the most reliable chromatin signature to predict cis-gene transcription in every human cell type examined. Targeted depletion of three cheRNAs decreases expression of their neighboring genes, indicating potential co-activator function, and single-molecule fluorescence in situ hybridization (smFISH) of one cheRNA-distal target gene pair suggests a spatial overlap consistent with a role in chromosome looping. Additionally, the cheRNA HIDALGO stimulates the fetal hemoglobin subunit gamma 1 (HBG1) gene during erythroid differentiation by promoting contacts to a downstream enhancer. Our results suggest that multiple cheRNAs activate proximal lineage-specific gene transcription.

Indexed as

Gene Expression RegulationTranscription, GeneticCell LineChromatinHumansRNA, Long NoncodingChromatinRNA, Long Noncoding

Identifiers

PMID28628087
PMCPMC5682930
OpenAlexW2625626396

What OpenQuestion holds

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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.