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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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 |
work_keys_str_mv |
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