Evidence map›Paper›PMID 30190464›Full record

ArticleNature communications2018

LincRNA H19 protects from dietary obesity by constraining expression of monoallelic genes in brown fat.

Elena Schmidt, Ines Dhaouadi, Isabella Gaziano, Matteo Oliverio, Paul Klemm, Motoharu Awazawa, Gerfried Mitterer, Eduardo Fernandez-Rebollo, Marta Pradas-Juni, Wolfgang Wagner and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 2% 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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 156 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  5. Advances in the Regulation of Lipid Metabolism by Non-Coding RNAs.Animals : an open access journal from MDPI · 2025
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  17. Pulling the trigger: Noncoding RNAs in white adipose tissue browning.Reviews in endocrine & metabolic disorders · 2024
    Review
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  20. Review

14 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

25 authors at 8 institutions in 3 countries.

Elena SchmidtMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.ORCID http://orcid.org/0000-0003-0829-1423
Ines DhaouadiMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Isabella GazianoMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Matteo OliverioMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.ORCID http://orcid.org/0000-0002-7969-2796
Paul KlemmMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Motoharu AwazawaMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Gerfried MittererDepartment of Laboratory Medicine, Medical University of Vienna, 1090, Vienna, Austria.
Eduardo Fernandez-RebolloDepartment for Biochemistry and Molecular Biology (BMB), University of Southern Denmark, Campusvej 55, 5230, Odense M, Denmark.
Marta Pradas-JuniMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Wolfgang WagnerHelmholtz-Institute for Biomedical Engineering, Stem Cell Biology and Cellular Engineering, RWTH Aachen University Medical School, Pauwelstrasse 20, 52074, Aachen, Germany.ORCID http://orcid.org/0000-0002-1971-3217
Philipp HammerschmidtMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Rute LoureiroMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Christoph KieferDepartment for Biochemistry and Molecular Biology (BMB), University of Southern Denmark, Campusvej 55, 5230, Odense M, Denmark.
Nils R HansmeierMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Sajjad KhaniMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany.
Matteo BergamiCologne Cluster of Excellence: Cellular Stress Responses in Ageing-associated Diseases (CECAD), Joseph-Stelzmann-Str. 26, 50931, Köln, Germany.
Markus HeineInstitute for Biochemistry and Molecular Cell Biology, Martinistraße 52, 20246, Hamburg, Germany.
Evgenia NtiniMax Planck Institute for Molecular Genetics, Ihnestrasse 63-73, 14195, Berlin, Germany.
Peter FrommoltCologne Cluster of Excellence: Cellular Stress Responses in Ageing-associated Diseases (CECAD), Joseph-Stelzmann-Str. 26, 50931, Köln, Germany.
Peter ZentisCologne Cluster of Excellence: Cellular Stress Responses in Ageing-associated Diseases (CECAD), Joseph-Stelzmann-Str. 26, 50931, Köln, Germany.
Ulf Andersson ØromInstitute for Molecular Biology and Genetics, Aarhus University, C F Møllers Alle 3, 8000, Aarhus C, Denmark.ORCID http://orcid.org/0000-0002-0643-0592
Jörg HeerenInstitute for Biochemistry and Molecular Cell Biology, Martinistraße 52, 20246, Hamburg, Germany.
Matthias BlüherDepartment of Medicine, University of Leipzig, 04103, Leipzig, Germany.
Martin BilbanDepartment of Laboratory Medicine, Medical University of Vienna, 1090, Vienna, Austria. martin.bilban@meduniwien.ac.at.
Jan-Wilhelm KornfeldMax Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931, Köln, Germany. janwilhelmkornfeld@bmb.sdu.dk.ORCID http://orcid.org/0000-0002-6802-4442
Max Planck Institute for Metabolism Research · DEUniversity of Southern Denmark · DKCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEMedical University of Vienna · ATAarhus University · DKLeipzig University · DEMax Planck Institute for Molecular Genetics · DERWTH Aachen University · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) KO4728/1-1EC | European Research Council (ERC) 675014
6 · The paper itself

Abstract

Increasing brown adipose tissue (BAT) thermogenesis in mice and humans improves metabolic health and understanding BAT function is of interest for novel approaches to counteract obesity. The role of long noncoding RNAs (lncRNAs) in these processes remains elusive. We observed maternally expressed, imprinted lncRNA H19 increased upon cold-activation and decreased in obesity in BAT. Inverse correlations of H19 with BMI were also observed in humans. H19 overexpression promoted, while silencing of H19 impaired adipogenesis, oxidative metabolism and mitochondrial respiration in brown but not white adipocytes. In vivo, H19 overexpression protected against DIO, improved insulin sensitivity and mitochondrial biogenesis, whereas fat H19 loss sensitized towards HFD weight gains. Strikingly, paternally expressed genes (PEG) were largely absent from BAT and we demonstrated that H19 recruits PEG-inactivating H19-MBD1 complexes and acts as BAT-selective PEG gatekeeper. This has implications for our understanding how monoallelic gene expression affects metabolism in rodents and, potentially, humans.

Indexed as

Genomic ImprintingAdipose Tissue, BrownAdipose Tissue, WhiteAdultAgedAged, 80 and overAnimalsDiet, High-FatEnergy MetabolismFemaleGene Expression RegulationHumansMaleMice, Inbred C57BLMice, TransgenicMiddle AgedH19 long non-coding RNARNA, Long Noncoding

Identifiers

PMID30190464
PMCPMC6127097
OpenAlexW2888811593

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.