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Harrer, P. ; Krygier, M.* ; Krenn, M.* ; Kittke, V. ; Danis, M.* ; Krastev, G.* ; Saparov, A. ; Pichon, V.* ; Malbos, M.* ; Scherer, C.* ; Dzinovic, I. ; Škorvánek, M.* ; Kopajtich, R. ; Prokisch, H. ; Silvaieh, S.* ; Grisold, A.* ; Mazurkiewicz-Bełdzińska, M.* ; de Sainte Agathe, J.M.* ; Winkelmann, J. ; Necpál, J.* ; Jech, R.* ; Zech, M.

Expanding the allelic and clinical heterogeneity of movement disorders linked to defects of mitochondrial adenosine triphosphate synthase.

Mov. Disord., DOI: 10.1002/mds.30209 (2025)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
BACKGROUND: Defects of mitochondrial ATP synthase (ATPase) represent an emerging, yet incompletely understood group of neurodevelopmental diseases with abnormal movements. OBJECTIVE: The aim of this study was to redefine the phenotypic and mutational spectrum of movement disorders linked to the ATPase subunit-encoding genes ATP5F1A and ATP5F1B. METHODS: We recruited regionally distant patients who had been genome or exome sequenced. Fibroblast cultures from two patients were established to perform RNA sequencing, immunoblotting, mass spectrometry-based high-throughput quantitative proteomics, and ATPase activity assays. In silico three-dimensional missense variant modeling was performed. RESULTS: We identified a patient with developmental delay, myoclonic dystonia, and spasticity who carried a heterozygous frameshift c.1404del (p.Glu469Serfs*3) variant in ATP5F1A. The patient's cells exhibited significant reductions in ATP5F1A mRNA, underexpression of the α-subunit of ATPase in association with other aberrantly expressed ATPase components, and compromised ATPase activity. In addition, a novel deleterious heterozygous ATP5F1A missense c.1252G>A (p.Gly418Arg) variant was discovered, shared by three patients from two families with hereditary spastic paraplegia (HSP). This variant mapped to a functionally important intersubunit communication site. A third heterozygous variant, c.1074+1G>T, affected a canonical donor splice site of ATP5F1B and resulted in exon skipping with significantly diminished ATP5F1B mRNA levels, as well as impaired ATPase activity. The associated phenotype consisted of cerebral palsy (CP) with prominent generalized dystonia. CONCLUSIONS: Our data confirm and expand the role of dominant ATP5F1A and ATP5F1B variants in neurodevelopmental movement disorders. ATP5F1A/ATP5F1B-related ATPase diseases should be considered as a cause of dystonia, HSP, and CP. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Atp Synthase ; Atp5f1a ; Atp5f1b ; Cerebral Palsy ; Dominant Variant ; Dystonia ; Mitochondrial Disease ; Spasticity; Atp Synthase; Pathogenicity; Mutations
ISSN (print) / ISBN 0885-3185
e-ISSN 1531-8257
Zeitschrift Movement Disorders
Verlag Wiley
Verlagsort 111 River St, Hoboken 07030-5774, Nj Usa
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Neurogenomics (ING)
Förderungen
DFG Grants WI
EJP RD
German Federal Ministry of Education and Research (BMBF, Bonn, Germany)
Else KroenerFresenius-Stiftung
BMBF
Free State of Bavaria
EU Renewal and Resilience Plan "Large projects for excellent researchers"
Czech Ministry of Health
National Institute for Neurological Research
European Union, Next Generation EU
DFG Research Infrastructure NGS_CC