Evidence map›Paper›PMID 31683747›Full record

ReviewInternational journal of molecular sciences2019

How Epigenetic Modifications Drive the Expression and Mediate the Action of PGC-1α in the Regulation of Metabolism.

Anne I Krämer, Christoph Handschin

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  19. Transcriptome-wide analysis of PGC-1α-binding RNAs identifies genes linked to glucagon metabolic action.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

2 authors.

Anne I KrämerBiozentrum, University of Basel, 4056 Basel, Switzerland. anne.kraemer@unibas.ch.
Christoph HandschinBiozentrum, University of Basel, 4056 Basel, Switzerland. christoph.handschin@unibas.ch.ORCID 0000-0003-0603-1097

Funding

European Research Council 616830-MUSCLE_NETKrebsforschung Schweiz KFS-3733-08-2015Novartis Stiftung für Medizinisch-Biologische Forschung 18C155Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 310030_184832Swiss Society for Research on Muscle Diseases n/aSystemsX.ch IPhD
6 · The paper itself

Abstract

Epigenetic changes are a hallmark of short- and long-term transcriptional regulation, and hence instrumental in the control of cellular identity and plasticity. Epigenetic mechanisms leading to changes in chromatin structure, accessibility for recruitment of transcriptional complexes, and interaction of enhancers and promoters all contribute to acute and chronic adaptations of cells, tissues and organs to internal and external perturbations. Similarly, the peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) is activated by stimuli that alter the cellular energetic demand, and subsequently controls complex transcriptional networks responsible for cellular plasticity. It thus is of no surprise that PGC-1α is under the control of epigenetic mechanisms, and constitutes a mediator of epigenetic changes in various tissues and contexts. In this review, we summarize the current knowledge of the link between epigenetics and PGC-1α in health and disease.

Indexed as

Epigenesis, GeneticGene Expression RegulationAdipose Tissue, BrownAnimalsDNA MethylationEnergy MetabolismHumansObesityPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanDNA methylationepigeneticsexercisegene regulationhistone modificationmetabolic diseasesmetabolismmicro RNAperoxisome proliferator-activated receptor γ coactivator 1α (PGC-1α)thermogenesis

Identifiers

PMID31683747
PMCPMC6862278

What OpenQuestion holds

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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.