Evidence map›Paper›PMID 39468638›Full record

ArticleActa neuropathologica communications2024

Genotype‒phenotype correlation in recessive DNAJB4 myopathy.

Michio Inoue, Divya Jayaraman, Rocio Bengoechea, Ankan Bhadra, Casie A Genetti, Abdulrahman A Aldeeri, Betül Turan, Rafael Adrian Pacheco-Orozco, Almundher Al-Maawali, Nadia Al Hashmi and 7 more

Abstract read
In one paragraph

Article in Acta neuropathologica communications, 2024. 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. Article
  2. DnaJB1 chaperone inhibits tau aggregation by recognizing its N-terminus.bioRxiv : the preprint server for biology · 2025
    Article
  3. Review
  4. Unlocking Disease-Modifying Treatments for TDP-43-Mediated Neurodegeneration.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Michio InoueDepartment of Neurology, Washington University School of Medicine, 4523 Clayton Avenue, Box 8111, Saint Louis, MO, 63110, USA. michio@wustl.edu.
Divya JayaramanDivision of Genetics and Genomics, Boston Children's Hospital, The Manton Center for Orphan Disease Research, Harvard Medical School, Boston, USA.
Rocio BengoecheaDepartment of Neurology, Washington University School of Medicine, 4523 Clayton Avenue, Box 8111, Saint Louis, MO, 63110, USA.
Ankan BhadraDepartment of Cell Biology and Physiology, Washington University School of Medicine, Saint Louis, USA.
Casie A GenettiDivision of Genetics and Genomics, Boston Children's Hospital, The Manton Center for Orphan Disease Research, Harvard Medical School, Boston, USA.
Abdulrahman A AldeeriDivision of Genetics and Genomics, Boston Children's Hospital, The Manton Center for Orphan Disease Research, Harvard Medical School, Boston, USA.
Betül TuranDepartment of Medical Genetics, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Rafael Adrian Pacheco-OrozcoOrganización Clinica General del Norte, Barranquilla, Colombia.
Almundher Al-MaawaliDepartment of Genetics, Sultan Qaboos University Hospital, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Nadia Al HashmiRoyal Hospital, National Genetic Center, Ministry of Health, Muscat, Oman.
Ayşe Gül ZamaniDepartment of Medical Genetics, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Emine GöktaşDepartment of Medical Genetics, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Sevgi PekcanDepartment of Pediatric Pulmonology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Hanife Tuğçe ÇağlarDepartment of Pediatric Pulmonology, Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Heather TrueDepartment of Cell Biology and Physiology, Washington University School of Medicine, Saint Louis, USA.
Alan H BeggsDivision of Genetics and Genomics, Boston Children's Hospital, The Manton Center for Orphan Disease Research, Harvard Medical School, Boston, USA.
Conrad C WeihlDepartment of Neurology, Washington University School of Medicine, 4523 Clayton Avenue, Box 8111, Saint Louis, MO, 63110, USA.

Funding

Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
Chaperone Dysfunction in Myopathy: Connecting Yeast Genetics with Mouse ModelsR01AR068797 · NIAMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L, WEIHL, CONRAD C · 2015 to 2025
$6.1M
CH/BIDMC/Harvard Medical School Neurology Resident Research Education Program Competing RenewalR25NS070682 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI PODURI, ANNAPURNA, SAPER, CLIFFORD B · 2010 to 2023
$4.5M
Clinical and Translational Studies in Muscle DiseaseK24AR073317 · NIAMS · WASHINGTON UNIVERSITY · PI CONRAD C WEIHL · 2018 to 2026
$1.6M
AUTOPHAGIC DYSFUNCTION IN IBMPFD ASSOCIATED MUSCLE DISEASEK02AG042095 · NIA · WASHINGTON UNIVERSITY · PI WEIHL, CONRAD C · 2012 to 2016
$671k
Elucidating the Role of DNAJ Proteins in Muscle DiseaseK99AR084062 · NIAMS · WASHINGTON UNIVERSITY · PI INOUE, MICHIO · 2024 to 2025
$196k
Eunice Kennedy Shriver National Institute of Child Health and Human Development P50HD105351Muscular Dystrophy Association MDA961862NIAMS NIH HHS K24 AR073317NIAMS NIH HHS K99 AR084062NIAMS NIH HHS K99AR084062NIAMS NIH HHS R01 AR068797NIAMS NIH HHS R01AR068797NIA NIH HHS K02 AG042095NICHD NIH HHS P50 HD105351NINDS NIH HHS R25 NS070682NINDS NIH HHS R25NS070682
6 · The paper itself

Abstract

Protein aggregate myopathies can result from pathogenic variants in genes encoding protein chaperones. DNAJB4 is a cochaperone belonging to the heat shock protein-40 (HSP40) family and plays a vital role in cellular proteostasis. Recessive loss-of-function variants in DNAJB4 cause myopathy with early respiratory failure and spinal rigidity, presenting from infancy to adulthood. This study investigated the broader clinical and genetic spectrum of DNAJB4 myopathy. In this study, we performed whole-exome sequencing on seven patients with early respiratory failure of unknown genetic etiology. We identified five distinct pathogenic variants in DNAJB4 in five unrelated families of diverse ethnic backgrounds: three loss-of-function variants (c.547 C > T, p.R183*; c.775 C > T, p.R259*; an exon 2 deletion) and two missense variants (c.105G > C, p.K35N; c.181 A > G, p.R61G). All patients were homozygous. Most affected individuals exhibited early respiratory failure, and patients from three families had rigid spine syndrome with axial weakness in proportion to appendicular weakness. Additional symptoms included dysphagia, ankle contractures, scoliosis, neck stiffness, and cardiac dysfunction. Notably, J-domain missense variants were associated with a more severe phenotype, including an earlier age of onset and a higher mortality rate, suggesting a strong genotype‒phenotype correlation. Consistent with a loss of function, the nonsense variants presented decreased stability. In contrast, the missense variants exhibited normal or increased stability but behaved as loss-of-function variants in yeast complementation and TDP-43 disaggregation assays. Our findings suggest that DNAJB4 is an emerging cause of myopathy with rigid spine syndrome of variable age of onset and severity. This diagnosis should be considered in individuals presenting with suggestive symptoms, particularly if they exhibit neck stiffness during infancy or experience respiratory failure in adults without significant limb muscle weakness. Missense variants in the J domain may predict a more severe phenotype.

Indexed as

Genetic Association StudiesHSP40 Heat-Shock ProteinsAdolescentAdultChildChild, PreschoolExome SequencingFemaleHumansMaleMallory BodiesMiddle AgedMolecular ChaperonesMuscular DiseasesMuscular DystrophiesPedigreeHSP40 Heat-Shock ProteinsMolecular ChaperonesChaperonopathyDNAJB4Heat shock proteinsProtein aggregate myopathyRespiratory failureRigid spine syndrome

Identifiers

PMID39468638
PMCPMC11514740

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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.