Evidence map›Paper›PMID 38386308›Full record

ArticleBrain : a journal of neurology2024

ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations.

Lucia Laugwitz, Fubo Cheng, Stephan C Collins, Alexander Hustinx, Nicolas Navarro, Simon Welsch, Helen Cox, Tzung-Chien Hsieh, Aswinkumar Vijayananth, Rebecca Buchert and 34 more

Open access · hybridAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Genes as Genome Stabilizers in Pluripotent Stem Cells.Advances in experimental medicine and biology · 2025
    Review
  7. Article
  8. Article
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

44 authors at 15 institutions in 4 countries.

Lucia LaugwitzInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.ORCID 0000-0003-2506-1961
Fubo ChengInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.ORCID 0000-0001-7215-8593
Stephan C CollinsInserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France.
Alexander HustinxInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany.
Nicolas NavarroBiogeosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, Dijon 2100, France.
Simon WelschDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany.
Helen CoxWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham B15 2TG, UK.
Tzung-Chien HsiehInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany.
Aswinkumar VijayananthInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany.
Rebecca BuchertInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Benjamin BenderDiagnostic and Interventional Neuroradiology, Radiologic Clinics, University of Tübingen, Tübingen 72076, Germany.
Stephanie EfthymiouDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.ORCID 0000-0003-4900-9877
David MurphyDepartment of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Faisal ZafarPediatric Neurology, Children's Hospital, Multan 60000, Pakistan.
Nuzhat RanaPediatric Neurology, Children's Hospital, Multan 60000, Pakistan.
Ute GrasshoffInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Ruth J FalbInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Mona GrimmelInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Annette SeibtDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany.
Wenxu ZhengInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Hamid GhaediDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran.
Marie ThirionInserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France.
Sébastien CouetteBiogeosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, Dijon 2100, France.
Reza AzizimalamiriDepartment of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz 6135715794, Iran.
Saeid SadeghianDepartment of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz 6135715794, Iran.ORCID 0000-0002-7935-3401
Hamid GalehdariDepartment of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz 6135783151, Iran.
Mina ZamaniDepartment of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz 6135783151, Iran.ORCID 0000-0002-7005-3787
Jawaher ZeighamiNarges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz 6155689467, Iran.
Alireza SedaghatNarges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz 6155689467, Iran.
Samira Molaei RamsheDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran.
Ali ZareDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran.
Behnam AlipoorDepartment of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj 7591741417, Iran.
Dirk KleeDepartment of Pediatric Radiology, Medical Faculty, Institute of Radiology, Heinrich-Heine-University, Düsseldorf 40225, Germany.
Marc SturmInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Henry HouldenDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.ORCID 0000-0002-2866-7777
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
Dagmar WieczorekMedical Faculty and University Hospital Düsseldorf, Institute of Human Genetics, Heinrich-Heine-University Düsseldorf, Düsseldorf 40225, Germany.
Ryan GavinWest Midlands Regional Genetics Laboratory, Central and South Genomic Laboratory Hub, Birmingham B15 2TG, UK.
Reza MaroofianDepartment of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.ORCID 0000-0001-6763-1542
Peter KrawitzInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany.ORCID 0000-0002-3194-8625
Binnaz YalcinInserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France.ORCID 0000-0002-1924-6807
Felix DistelmaierDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany.
Tobias B HaackInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.
University of Tübingen · DEHeinrich Heine University Düsseldorf · DENational Hospital for Neurology and Neurosurgery · GBUniversity of Bonn · DEAhvaz Jundishapur University of Medical Sciences · IRInserm · FRShahid Beheshti University of Medical Sciences · IRCentre National de la Recherche Scientifique · FRShahid Chamran University of Ahvaz · IRBernstein Center for Computational Neuroscience Tübingen · DEBirmingham Women’s and Children’s NHS Foundation Trust · GBDüsseldorf University Hospital · DEQueen Mary University of London · GBWessex Regional Genetics Laboratory · GBYasuj University of Medical Sciences · IR

Funding

Deutsche Forschungsgemeinschaft 418081722European Regional Development Fund 3HP-HP-FPA ERN-01-2016/739516French National Research AgencyNational Institute of Health and Medical ResearchWellcome Trust
6 · The paper itself

Abstract

Neurodevelopmental disorders are major indications for genetic referral and have been linked to more than 1500 loci including genes encoding transcriptional regulators. The dysfunction of transcription factors often results in characteristic syndromic presentations; however, at least half of these patients lack a genetic diagnosis. The implementation of machine learning approaches has the potential to aid in the identification of new disease genes and delineate associated phenotypes. Next generation sequencing was performed in seven affected individuals with neurodevelopmental delay and dysmorphic features. Clinical characterization included reanalysis of available neuroimaging datasets and 2D portrait image analysis with GestaltMatcher. The functional consequences of ZSCAN10 loss were modelled in mouse embryonic stem cells (mESCs), including a knockout and a representative ZSCAN10 protein truncating variant. These models were characterized by gene expression and western blot analyses, chromatin immunoprecipitation and quantitative PCR (ChIP-qPCR) and immunofluorescence staining. Zscan10 knockout mouse embryos were generated and phenotyped. We prioritized bi-allelic ZSCAN10 loss-of-function variants in seven affected individuals from five unrelated families as the underlying molecular cause. RNA-sequencing analyses in Zscan10-/- mESCs indicated dysregulation of genes related to stem cell pluripotency. In addition, we established in mESCs the loss-of-function mechanism for a representative human ZSCAN10 protein truncating variant by showing alteration of its expression levels and subcellular localization, interfering with its binding to DNA enhancer targets. Deep phenotyping revealed global developmental delay, facial asymmetry and malformations of the outer ear as consistent clinical features. Cerebral MRI showed dysplasia of the semicircular canals as an anatomical correlate of sensorineural hearing loss. Facial asymmetry was confirmed as a clinical feature by GestaltMatcher and was recapitulated in the Zscan10 mouse model along with inner and outer ear malformations. Our findings provide evidence of a novel syndromic neurodevelopmental disorder caused by bi-allelic loss-of-function variants in ZSCAN10.

Indexed as

Mice, KnockoutNeurodevelopmental DisordersAdolescentAnimalsChildChild, PreschoolDNA-Binding ProteinsFemaleHumansInfantMaleMiceTranscription FactorsDNA-Binding ProteinsTranscription FactorsZSCAN10 protein, humanZscan10 protein, mouseneurodevelopmental disordersoto-facial syndromesemicircular canal dysplasiazinc finger transcription factor

Identifiers

PMID38386308
PMCPMC11224597
OpenAlexW4392028090

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.