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Skeletal muscle DNMT3A plays a necessary role in endurance exercise by regulating oxidative capacity of red muscles

https://doi.org/10.1101/2020.05.18.102400

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1 of the 96 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1074/jbc.m110.211466 (notice 2020-11-23).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Physical Exercise for Muscle Atrophy

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Methods of microphotometric assay of succinate dehydrogenase and cytochromec oxidase activities for use on human skeletal muscle

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Skeletal Muscle: A Brief Review of Structure and Function

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Free Radicals: Properties, Sources, Targets, and Their Implication in Various Diseases

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Skeletal muscle wasting in cachexia and sarcopenia: molecular pathophysiology and impact of exercise training

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Physical Exercise and Epigenetic Modifications in Skeletal Muscle

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The NADPH oxidase of professional phagocytes—prototype of the NOX electron transport chain systems

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Mitochondrial dysfunction and oxidative stress in metabolic disorders — A step towards mitochondria based therapeutic strategies

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Skeletal muscle mitochondria: A major player in exercise, health and disease

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FDH: An aldehyde dehydrogenase fusion enzyme in folate metabolism

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Mitochondrial ROS production

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Integrative Biology of Exercise

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mRNA Expression Signatures of Human Skeletal Muscle Atrophy Identify a Natural Compound that Increases Muscle Mass

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Acute Exercise Remodels Promoter Methylation in Human Skeletal Muscle

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Brown Adipose Tissue Controls Skeletal Muscle Function via the Secretion of Myostatin

inferredcites →https://doi.org/10.1016/j.cophys.2019.05.011openalex-snapshot

Exercise intolerance in patients with mitochondrial myopathies: perfusive and diffusive limitations in the O2 pathway

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2016.05.011openalex-snapshot

Regulation of NADPH oxidases in skeletal muscle

inferredcites →https://doi.org/10.1016/j.redox.2015.08.010openalex-snapshot

Calcium and ROS: A mutual interplay

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Reactive oxygen species and mitochondria: A nexus of cellular homeostasis

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Skeletal muscle: Energy metabolism, fiber types, fatigue and adaptability

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Distribution of Marker Enzymes between Mesosomal and Protoplast Membranes

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Methylation-Induced Repression— Belts, Braces, and Chromatin

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A Muscle-Specific Insulin Receptor Knockout Exhibits Features of the Metabolic Syndrome of NIDDM without Altering Glucose Tolerance

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The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

inferredcites →https://doi.org/10.1038/cmi.2014.89openalex-snapshot

NADPH oxidases: an overview from structure to innate immunity-associated pathologies

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Dnmt3a is essential for hematopoietic stem cell differentiation

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Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

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Baf60c drives glycolytic metabolism in the muscle and improves systemic glucose homeostasis through Deptor-mediated Akt activation

inferredcites →https://doi.org/10.1038/nm.3774openalex-snapshot

DNA methyltransferase 3a regulates osteoclast differentiation by coupling to an S-adenosylmethionine–producing metabolic pathway

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HISAT: a fast spliced aligner with low memory requirements

inferredcites →https://doi.org/10.1038/nrm4043openalex-snapshot

DNA methylation pathways and their crosstalk with histone methylation

inferredcites →https://doi.org/10.1038/s41467-019-12523-9openalex-snapshot

Cytosolic ROS production by NADPH oxidase 2 regulates muscle glucose uptake during exercise

inferredcites →https://doi.org/10.1038/s41584-019-0296-5openalex-snapshot

CCL21–CCR7 axis in RA: linking inflammation and bone erosion

inferredcites →https://doi.org/10.1038/sdata.2018.213openalex-snapshot

Methylome of human skeletal muscle after acute & chronic resistance exercise training, detraining & retraining

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Kruppel-like factor 15 regulates skeletal muscle lipid flux and exercise adaptation

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Exercise Increases Mitochondrial PGC-1α Content and Promotes Nuclear-Mitochondrial Cross-talk to Coordinate Mitochondrial Biogenesis

inferredcites →https://doi.org/10.1074/jbc.m112.374777openalex-snapshot

Stress-induced Skeletal Muscle Gadd45a Expression Reprograms Myonuclei and Causes Muscle Atrophy

inferredcites →https://doi.org/10.1074/jbc.m113.511535openalex-snapshot

Targeted Metabolomics Connects Thioredoxin-interacting Protein (TXNIP) to Mitochondrial Fuel Selection and Regulation of Specific Oxidoreductase Enzymes in Skeletal Muscle

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A Transverse Tubule NADPH Oxidase Activity Stimulates Calcium Release from Isolated Triads via Ryanodine Receptor Type 1 S -Glutathionylation

inferredcites →https://doi.org/10.1089/ars.2012.4623openalex-snapshot

Studies of Mitochondrial and Nonmitochondrial Sources Implicate Nicotinamide Adenine Dinucleotide Phosphate Oxidase(s) in the Increased Skeletal Muscle Superoxide Generation That Occurs During Contractile Activity

inferredcites →https://doi.org/10.1089/ars.2013.5773openalex-snapshot

Exercise-Induced Skeletal Muscle Remodeling and Metabolic Adaptation: Redox Signaling and Role of Autophagy

inferredcites →https://doi.org/10.1093/jmcb/mjy066openalex-snapshot

The HDAC3 enzymatic activity regulates skeletal muscle fuel metabolism

inferredcites →https://doi.org/10.1111/bph.13403openalex-snapshot

Crosstalk of mitochondria with NADPH oxidase via reactive oxygen and nitrogen species signalling and its role for vascular function

inferredcites →https://doi.org/10.1111/j.1475-097x.1983.tb00704.xopenalex-snapshot

The ageing muscle

inferredcites →https://doi.org/10.1113/expphysiol.2009.050526openalex-snapshot

Reactive oxygen species are signalling molecules for skeletal muscle adaptation

inferredcites →https://doi.org/10.1126/science.1202768openalex-snapshot

X-ROS Signaling: Rapid Mechano-Chemo Transduction in Heart

inferredcites →https://doi.org/10.1128/mcb.9.8.3393openalex-snapshot

Muscle Creatine Kinase Sequence Elements Regulating Skeletal and Cardiac Muscle Expression in Transgenic Mice

inferredcites →https://doi.org/10.1136/bjsports-2014-094073openalex-snapshot

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inferredcites →https://doi.org/10.1146/annurev-physiol-020518-114310openalex-snapshot

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inferredcites →https://doi.org/10.1146/annurev.ph.38.030176.001421openalex-snapshot

Biochemical Adaptations to Endurance Exercise in Muscle

inferredcites →https://doi.org/10.1152/ajpendo.00289.2014openalex-snapshot

Exercise training alters DNA methylation patterns in genes related to muscle growth and differentiation in mice

inferredcites →https://doi.org/10.1152/ajpendo.00380.2013openalex-snapshot

Skeletal muscle denervation causes skeletal muscle atrophy through a pathway that involves both Gadd45a and HDAC4

inferredcites →https://doi.org/10.1152/ajpregu.00767.2006openalex-snapshot

Denervation-induced skeletal muscle atrophy is associated with increased mitochondrial ROS production

inferredcites →https://doi.org/10.1152/jappl.2001.90.5.1936openalex-snapshot

Intracellular signaling specificity in skeletal muscle in response to different modes of exercise

inferredcites →https://doi.org/10.1152/japplphysiol.00857.2014openalex-snapshot

Effects of sleeping with reduced carbohydrate availability on acute training responses

inferredcites →https://doi.org/10.1152/japplphysiol.01145.2006openalex-snapshot

The role of free radicals in the pathophysiology of muscular dystrophy

inferredcites →https://doi.org/10.1152/physrev.00031.2010openalex-snapshot

Fiber Types in Mammalian Skeletal Muscles

inferredcites →https://doi.org/10.1152/physrev.00035.2013openalex-snapshot

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inferredcites →https://doi.org/10.1155/2012/217037openalex-snapshot

Reactive Oxygen Species, Oxidative Damage, and Antioxidative Defense Mechanism in Plants under Stressful Conditions

inferredcites →https://doi.org/10.1155/2012/756132openalex-snapshot

Oxidants, Antioxidants, and the Beneficial Roles of Exercise-Induced Production of Reactive Species

inferredcites →https://doi.org/10.1155/2016/1245049openalex-snapshot

Role of ROS and RNS Sources in Physiological and Pathological Conditions

inferredcites →https://doi.org/10.1155/2019/7058350openalex-snapshot

Stay Fit, Stay Young: Mitochondria in Movement: The Role of Exercise in the New Mitochondrial Paradigm

inferredcites →https://doi.org/10.1159/000445156openalex-snapshot

Metabolic Effects of Exercise

inferredcites →https://doi.org/10.1159/000484889openalex-snapshot

Study of HSPB6: Insights into the Properties of the Multifunctional Protective Agent

inferredcites →https://doi.org/10.1161/circresaha.118.310082openalex-snapshot

Calcium Signaling and Reactive Oxygen Species in Mitochondria

inferredcites →https://doi.org/10.1172/jci37662openalex-snapshot

Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-β

inferredcites →https://doi.org/10.1179/1351000213y.0000000077openalex-snapshot

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inferredcites →https://doi.org/10.1186/s12864-017-4193-5openalex-snapshot

Physical activity in the prevention of human diseases: role of epigenetic modifications

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1194/jlr.p028910openalex-snapshot

PPARγ coactivator-1α contributes to exercise-induced regulation of intramuscular lipid droplet programming in mice and humans

inferredcites →https://doi.org/10.1242/dmm.010389openalex-snapshot

Cellular and molecular mechanisms of muscle atrophy

inferredcites →https://doi.org/10.1242/jcs.200642openalex-snapshot

HIRA deficiency in muscle fibers causes hypertrophy and susceptibility to oxidative stress

inferredcites →https://doi.org/10.1242/jeb.098863openalex-snapshot

Skeletal Muscle Fuel Selection Occurs at the Mitochondrial Level

inferredcites →https://doi.org/10.1249/jes.0000000000000025openalex-snapshot

Mitochondrial Plasticity with Exercise Training and Extreme Environments

inferredcites →https://doi.org/10.12965/jer.1836268.134openalex-snapshot

Role of exercise in age-related sarcopenia

inferredcites →https://doi.org/10.1371/journal.pone.0041817openalex-snapshot

PGC-1α is Dispensable for Exercise-Induced Mitochondrial Biogenesis in Skeletal Muscle

inferredcites →https://doi.org/10.1371/journal.pone.0103044openalex-snapshot

The Relationship between Muscle Fiber Type-Specific PGC-1α Content and Mitochondrial Content Varies between Rodent Models and Humans

inferredcites →https://doi.org/10.18632/oncotarget.10744openalex-snapshot

NADPH: new oxygen for the ROS theory of aging

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Impact of an Exercise Intervention on DNA Methylation in Skeletal Muscle From First-Degree Relatives of Patients With Type 2 Diabetes

inferredcites →https://doi.org/10.2337/dc10-9990openalex-snapshot

Exercise and Type 2 Diabetes

inferredcites →https://doi.org/10.3109/10520299009105613openalex-snapshot

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Editorial: Mitochondria in Skeletal Muscle Health, Aging and Diseases

inferredcites →https://doi.org/10.3389/fphys.2016.00486openalex-snapshot

Redox Mechanism of Reactive Oxygen Species in Exercise

inferredcites →https://doi.org/10.3390/biom5020356openalex-snapshot

Impact of Oxidative Stress on Exercising Skeletal Muscle

inferredcites →https://doi.org/10.3390/ijms20071644openalex-snapshot

Calcium Release from Endoplasmic Reticulum Involves Calmodulin-Mediated NADPH Oxidase-Derived Reactive Oxygen Species Production in Endothelial Cells

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Apocynin: Chemical and Biophysical Properties of a NADPH Oxidase Inhibitor

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Regulation of Muscle Glycogen Metabolism during Exercise: Implications for Endurance Performance and Training Adaptations

inferredcites →https://doi.org/10.4081/ejtm.2015.5272openalex-snapshot

Biology of muscle atrophy and of its recovery by FES in aging and mobility impairments: roots and by-products

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2174/0929867330666230607124803openalex-snapshot

An Updated Review on the Significance of DNA and Protein Methyltransferases and De-methylases in Human Diseases: From Molecular Mechanism to Novel Therapeutic Approaches

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.