Evidence map›Paper›PMID 30778059›Full record

ArticleNature communications2019

Long non-coding RNAs discriminate the stages and gene regulatory states of human humoral immune response.

Xabier Agirre, Cem Meydan, Yanwen Jiang, Leire Garate, Ashley S Doane, Zhuoning Li, Akanksha Verma, Bruno Paiva, José I Martín-Subero, Olivier Elemento and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing 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

71 citing papers in PubMed.

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  14. The role of circular RNAs in autoimmune diseases: Potential diagnostic biomarkers and therapeutic targets.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  15. Article
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  18. Review
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  20. Review

11 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

13 authors.

Xabier AgirreDepartment of Medicine, Division of Hematology/Oncology, Weill Cornell Medicine, New York, NY, 10021, USA. xaguirre@unav.es.
Cem MeydanDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.ORCID http://orcid.org/0000-0002-0663-6216
Yanwen JiangDepartment of Medicine, Division of Hematology/Oncology, Weill Cornell Medicine, New York, NY, 10021, USA.
Leire GarateDivision of Hemato-Oncology, Center for Applied Medical Research (CIMA), University of Navarra, IDISNA, Ciberonc, Pamplona, 31008, Spain.
Ashley S DoaneThe Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, 10021, USA.
Zhuoning LiDepartment of Medicine, Division of Hematology/Oncology, Weill Cornell Medicine, New York, NY, 10021, USA.
Akanksha VermaThe Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, 10021, USA.
Bruno PaivaDivision of Hemato-Oncology, Center for Applied Medical Research (CIMA), University of Navarra, IDISNA, Ciberonc, Pamplona, 31008, Spain.
José I Martín-SuberoInstitut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, 08036, Spain.
Olivier ElementoDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA.
Christopher E MasonDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, 10065, USA. chm2042@med.cornell.edu.ORCID http://orcid.org/0000-0002-1850-1642
Felipe ProsperDivision of Hemato-Oncology, Center for Applied Medical Research (CIMA), University of Navarra, IDISNA, Ciberonc, Pamplona, 31008, Spain. fprosper@unav.es.
Ari MelnickDepartment of Medicine, Division of Hematology/Oncology, Weill Cornell Medicine, New York, NY, 10021, USA. amm2014@med.cornell.edu.ORCID http://orcid.org/0000-0002-8074-2287

Funding

Targeting Epigenetic Circuits in B-Cell LymphomasR35CA220499 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2018 to 2024
$7.2M
Use of chromatin accessibility maps to discover novel regulatory circuits in aggressive B cell lymphomasF31CA220981 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DOANE, ASHLEY STEPHEN · 2017 to 2018
$89k
NCI NIH HHS F31 CA220981NCI NIH HHS R35 CA220499
6 · The paper itself

Abstract

lncRNAs make up a majority of the human transcriptome and have key regulatory functions. Here we perform unbiased de novo annotation of transcripts expressed during the human humoral immune response to find 30% of the human genome transcribed during this process, yet 58% of these transcripts manifest striking differential expression, indicating an lncRNA phylogenetic relationship among cell types that is more robust than that of coding genes. We provide an atlas of lncRNAs in naive and GC B-cells that indicates their partition into ten functionally categories based on chromatin features, DNase hypersensitivity and transcription factor localization, defining lncRNAs classes such as enhancer-RNAs (eRNA), bivalent-lncRNAs, and CTCF-associated, among others. Specifically, eRNAs are transcribed in 8.6% of regular enhancers and 36.5% of super enhancers, and are associated with coding genes that participate in critical immune regulatory pathways, while plasma cells have uniquely high levels of circular-RNAs accounted for by and reflecting the combinatorial clonal state of the Immunoglobulin loci.

Indexed as

B-LymphocytesEnhancer Elements, GeneticGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksGenome, HumanHumansImmunity, HumoralRNARNA, CircularRNA, Long NoncodingRNARNA, CircularRNA, Long Noncoding

Identifiers

PMID30778059
PMCPMC6379396

What OpenQuestion holds

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Registered trials

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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.