Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity

Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase, are the primary genetic cause for rapid-onset dystonia-parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). Recently, cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorin...

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Main Authors: Elinor Lazarov, Merle Hillebrand, Simone Schröder, Katharina Ternka, Julia Hofhuis, Andreas Ohlenbusch, Alonso Barrantes-Freer, Luis A. Pardo, Marlene U. Fruergaard, Poul Nissen, Knut Brockmann, Jutta Gärtner, Hendrik Rosewich
Format: Article
Language:English
Published: Elsevier 2020-09-01
Series:Neurobiology of Disease
Subjects:
AHC
RDP
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996120302874
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spelling doaj-d89e933f34624e70b8ae148a621dfa362021-03-22T08:42:13ZengElsevierNeurobiology of Disease1095-953X2020-09-01143105012Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov0Merle Hillebrand1Simone Schröder2Katharina Ternka3Julia Hofhuis4Andreas Ohlenbusch5Alonso Barrantes-Freer6Luis A. Pardo7Marlene U. Fruergaard8Poul Nissen9Knut Brockmann10Jutta Gärtner11Hendrik Rosewich12University Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyInstitute of Neuropathology, University Medical Centre, Göttingen, GermanyDepartment of Molecular Biology of Neuronal Signals, Max Planck Institute of Experimental Medicine, Göttingen, GermanyDANDRITE - Nordic EMBL Partnership for Molecular Medicine, Dept. Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10C, DK-8000 Aarhus C, DenmarkDANDRITE - Nordic EMBL Partnership for Molecular Medicine, Dept. Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10C, DK-8000 Aarhus C, DenmarkUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, GermanyUniversity Medical Center Göttingen, Georg August University, Department of Pediatrics and Adolescent Medicine, Division of Pediatric Neurology, Germany; Corresponding author.Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase, are the primary genetic cause for rapid-onset dystonia-parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). Recently, cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorineural hearing loss (CAPOS), early infantile epileptic encephalopathy (EIEE), childhood rapid onset ataxia (CROA) and relapsing encephalopathy with rapid onset ataxia (RECA) extend the clinical spectrum of ATP1A3 related disorders. AHC and RDP demonstrate distinct clinical features, with AHC symptoms being generally more severe compared to RDP. Currently, it is largely unknown what determines the disease severity, and whether severity is linked to the degree of functional impairment of the α3 subunit.Here we compared the effect of twelve different RDP and AHC specific mutations on the expression and function of the α3 Na+/K+-ATPase in transfected HEK cells and oocytes. All studied mutations led to functional impairment of the pump, as reflected by lower survival rate and reduced pump current. No difference in the extent of impairment, nor in the expression level, was found between the two phenotypes, suggesting that these measures of pump dysfunction do not exclusively determine the disease severity.http://www.sciencedirect.com/science/article/pii/S0969996120302874ParkinsonismAlternating hemiplegia of childhoodAHCRapid-onset dystonia-parkinsonismRDPATP1A3
collection DOAJ
language English
format Article
sources DOAJ
author Elinor Lazarov
Merle Hillebrand
Simone Schröder
Katharina Ternka
Julia Hofhuis
Andreas Ohlenbusch
Alonso Barrantes-Freer
Luis A. Pardo
Marlene U. Fruergaard
Poul Nissen
Knut Brockmann
Jutta Gärtner
Hendrik Rosewich
spellingShingle Elinor Lazarov
Merle Hillebrand
Simone Schröder
Katharina Ternka
Julia Hofhuis
Andreas Ohlenbusch
Alonso Barrantes-Freer
Luis A. Pardo
Marlene U. Fruergaard
Poul Nissen
Knut Brockmann
Jutta Gärtner
Hendrik Rosewich
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
Neurobiology of Disease
Parkinsonism
Alternating hemiplegia of childhood
AHC
Rapid-onset dystonia-parkinsonism
RDP
ATP1A3
author_facet Elinor Lazarov
Merle Hillebrand
Simone Schröder
Katharina Ternka
Julia Hofhuis
Andreas Ohlenbusch
Alonso Barrantes-Freer
Luis A. Pardo
Marlene U. Fruergaard
Poul Nissen
Knut Brockmann
Jutta Gärtner
Hendrik Rosewich
author_sort Elinor Lazarov
title Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
title_short Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
title_full Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
title_fullStr Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
title_full_unstemmed Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity
title_sort comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism atp1a3 mutations reveals functional deficits, which do not correlate with disease severity
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2020-09-01
description Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase, are the primary genetic cause for rapid-onset dystonia-parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). Recently, cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorineural hearing loss (CAPOS), early infantile epileptic encephalopathy (EIEE), childhood rapid onset ataxia (CROA) and relapsing encephalopathy with rapid onset ataxia (RECA) extend the clinical spectrum of ATP1A3 related disorders. AHC and RDP demonstrate distinct clinical features, with AHC symptoms being generally more severe compared to RDP. Currently, it is largely unknown what determines the disease severity, and whether severity is linked to the degree of functional impairment of the α3 subunit.Here we compared the effect of twelve different RDP and AHC specific mutations on the expression and function of the α3 Na+/K+-ATPase in transfected HEK cells and oocytes. All studied mutations led to functional impairment of the pump, as reflected by lower survival rate and reduced pump current. No difference in the extent of impairment, nor in the expression level, was found between the two phenotypes, suggesting that these measures of pump dysfunction do not exclusively determine the disease severity.
topic Parkinsonism
Alternating hemiplegia of childhood
AHC
Rapid-onset dystonia-parkinsonism
RDP
ATP1A3
url http://www.sciencedirect.com/science/article/pii/S0969996120302874
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