Evidence map›Paper›PMID 40302207›Full record

ArticleBrain : a journal of neurology2026

Pleiotropic effects of MORC2 derive from its epigenetic signature.

Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, Robert Kopajtich, Masahiro Ando, Enrico Bertini, Rosalba Carrozzo, Daria Diodato, Felix Distelmaier, Fang Fang and 22 more

Abstract read
In one paragraph

Article in Brain : a journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease.Annals of clinical and translational neurology · 2026
    Article
  2. Dystonia: Insights into Mechanisms and Novel Therapeutics.Current neurology and neuroscience reports · 2026
    Review
  3. NovelFrontiers in medicine · 2026
    Article
  4. Review
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

32 authors.

Fatemeh PeymaniInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Tomohiro EbiharaInstitute of Neurogenomics, Computational Health Center, Helmholtz Munich, Neuherberg 85764, Germany.
Dmitrii SmirnovInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Robert KopajtichInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Masahiro AndoDepartment of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
Enrico BertiniNeuromuscular Disorders Research Unit, Bambino Gesù Children's Hospital IRCCS, Rome 00165, Italy.ORCID 0000-0001-9276-4590
Rosalba CarrozzoLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome 00165, Italy.ORCID 0000-0002-3327-4054
Daria DiodatoNeuromuscular Disorders Research Unit, Bambino Gesù Children's Hospital IRCCS, Rome 00165, Italy.
Felix DistelmaierDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Heinrich-Heine-University Düsseldorf, Düsseldorf 40225, Germany.ORCID 0000-0001-8460-3738
Fang FangDepartment of Neurology, Beijing Children's Hospital, Capital Medical University, Beijing 100005, China.
Daniele GhezziUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano 20133, Italy.ORCID 0000-0002-6564-3766
Maja HempelInstitute of Human Genetics, Heidelberg University, Heidelberg 69120, Germany.
Katarzyna Iwanicka-PronickaDepartment of Medical Genetics, The Children's Memorial Health Institute, Warsaw 04-730, Poland.
Thomas KlopstockDepartment of Neurology, Friedrich-Baur-Institute, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich 81377, Germany.
Sarah L StentonInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Costanza LampertiUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano 20133, Italy.
Zhimei LiuDepartment of Neurology, Beijing Children's Hospital, Capital Medical University, Beijing 100005, China.
Aysylu MurtazinaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Yuji OkamotoDepartment of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
Yasushi OkazakiDiagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan.
Dorota Piekutowska-AbramczukDepartment of Medical Genetics, The Children's Memorial Health Institute, Warsaw 04-730, Poland.
Agnés RötigUMR1163, Université Paris Descartes, Sorbonne Paris Cité, Institut Imagine, Paris 75015, France.ORCID 0000-0003-0589-0703
Oxana RyzhkovaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Christian SchleinInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg 20246, Germany.
Olga ShaginaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Hiroshi TakashimaDepartment of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
Polina TsygankovaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Michael ZechInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Thomas MeitingerInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Masaru ShimuraInstitute of Neurogenomics, Computational Health Center, Helmholtz Munich, Neuherberg 85764, Germany.
Kei MurayamaDiagnostics and Therapeutics of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan.ORCID 0000-0002-3923-8636
Holger ProkischInstitute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.

Funding

AMED 201442014AAMED 201442071AAMED 23ek0109625AMED 23ek0109636AMED 24lk0221189s0301Bavarian Ministry of Health, Care and Prevention DMB-1805-0002BMBF 01GM1906BBMBF 01GM1920ABMBF 01GM2302BMBF 01KU2016ADZKJ 01GL2406BElse Kröner-Fresenius-Stiftung 2022_EKSE.185Elterninitiative Kinderkrebsklinik e.V. 450149205-TRR333/1Elterninitiative Kinderkrebsklinik e.V. #701900167Elterninitiative Kinderkrebsklinik e.V. SCHL2276/2-1German Research Foundation DFG 458949627German Research Foundation DI 1731/2-3German Research Foundation ZE 1213/2-1Horizon 2020 101080997Institute for Advanced StudyJapan Agency for Medical Research and DevelopmentJapan Society for the Promotion of Science JP18H02742Japan Society for the Promotion of Science JP20K16604Japan Society for the Promotion of Science JP21H02842Japan Society for the Promotion of Science JP21K15702Japan Society for the Promotion of Science JP22K07495Japan Society for the Promotion of Science JP22K07519Japan Society for the Promotion of Science JP22K15713Japan Society for the Promotion of Science JP23K06931Japan Society for the Promotion of Science JP23K06966Japan Society for the Promotion of Science JP24K18708Ministry of Health, Labor and Welfare 2016100002BResearch Committee for Ataxic DiseaseTechnical University of Munich
6 · The paper itself

Abstract

Heterozygous missense mutations in MORC2 have been implicated in various clinical entities, ranging from early-onset neurodevelopmental disorders to late-onset neuropathies. The mechanism underlying the phenotypic heterogeneity and pleiotropic effects of MORC2 has remained elusive. Here, we analysed blood and fibroblast DNA methylation, transcriptomes, proteomes and phenotypes of 53 MORC2 patients. We identified a MORC2-specific DNA methylation episignature that is universal across all MORC2-associated phenotypes and conserved across different tissues. The MORC2 episignature consists mainly of DNA hypermethylation in promoter regions, leading to transcriptional repression of target genes resulting in a MORC2-specific RNA signature. Concomitant downregulation of three disease-associated genes-ERCC8, NDUFAF2 and FKTN-at different levels mirrors the variable biochemical defects and clinical manifestations observed in MORC2 patients. Silencing of NDUFAF2 accounts for the Leigh syndrome manifestation, whereas dysmorphic features are due to the repression of ERCC8. Overall, we showed that pathogenic MORC2 variants cause specific episignature, whereby methylation level variability and its repression impact on target genes explains the pleiotropy and predicts phenotypic heterogeneity in MORC2-related disorders. We predict that epigenetic variation may underlie pleiotropy in other Mendelian disorders.

Indexed as

Epigenesis, GeneticGenetic PleiotropyTranscription FactorsDNA MethylationFemaleHumansMaleMutation, MissensePhenotypeTranscription FactorsCMTepisignatureLeigh syndromeMORC2multi-omicspleiotropy

Identifiers

PMID40302207
PMCPMC12782172

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.