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Article: MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital Long QT Syndrome: insights in the mechanism of action of protective modifier genes

TitleMTMR4 SNVs modulate ion channel degradation and clinical severity in congenital Long QT Syndrome: insights in the mechanism of action of protective modifier genes
Authors
KeywordsLong QT syndrome
Induced pluripotent stem cells
Arrhythmias
Variants
Nedd4L
Issue Date2021
PublisherOxford University Press. The Journal's web site is located at http://cardiovascres.oxfordjournals.org
Citation
Cardiovascular Research, 2021, v. 117 n. 3, p. 767-779 How to Cite?
AbstractAims: In long QT syndrome (LQTS) patients, modifier genes modulate the arrhythmic risk associated with a disease-causing mutation. Their recognition can improve risk stratification and clinical management, but their discovery represents a challenge. We tested whether a cellular-driven approach could help to identify new modifier genes and especially their mechanism of action. Methods and results: We generated human-induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM) from two patients carrying the same KCNQ1-Y111C mutation, but presenting opposite clinical phenotypes. We showed that the phenotype of the iPSC-CMs derived from the symptomatic patient is due to impaired trafficking and increased degradation of the mutant KCNQ1 and wild-type human ether-a-go-go-related gene. In the iPSC-CMs of the asymptomatic (AS) patient, the activity of an E3 ubiquitin-protein ligase (Nedd4L) involved in channel protein degradation was reduced and resulted in a decreased arrhythmogenic substrate. Two single-nucleotide variants (SNVs) on the Myotubularin-related protein 4 (MTMR4) gene, an interactor of Nedd4L, were identified by whole-exome sequencing as potential contributors to decreased Nedd4L activity. Correction of these SNVs by CRISPR/Cas9 unmasked the LQTS phenotype in AS cells. Importantly, the same MTMR4 variants were present in 77% of AS Y111C mutation carriers of a separate cohort. Thus, genetically mediated interference with Nedd4L activation seems associated with protective effects. Conclusion: Our finding represents the first demonstration of the cellular mechanism of action of a protective modifier gene in LQTS. It provides new clues for advanced risk stratification and paves the way for the design of new therapies targeting this specific molecular pathway.
Persistent Identifierhttp://hdl.handle.net/10722/214376
ISSN
2023 Impact Factor: 10.2
2023 SCImago Journal Rankings: 2.809
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLee, Y-K-
dc.contributor.authorSala, L-
dc.contributor.authorMura, M-
dc.contributor.authorRocchetti, M-
dc.contributor.authorPedrazzini, M-
dc.contributor.authorRan, X-
dc.contributor.authorMak, TSH-
dc.contributor.authorCrotti, L-
dc.contributor.authorSham, PC-
dc.contributor.authorTorre, E-
dc.contributor.authorZaza, A-
dc.contributor.authorSchwartz, PJ-
dc.contributor.authorTse, H-F-
dc.contributor.authorGnecchi, M-
dc.date.accessioned2015-08-21T11:21:02Z-
dc.date.available2015-08-21T11:21:02Z-
dc.date.issued2021-
dc.identifier.citationCardiovascular Research, 2021, v. 117 n. 3, p. 767-779-
dc.identifier.issn0008-6363-
dc.identifier.urihttp://hdl.handle.net/10722/214376-
dc.description.abstractAims: In long QT syndrome (LQTS) patients, modifier genes modulate the arrhythmic risk associated with a disease-causing mutation. Their recognition can improve risk stratification and clinical management, but their discovery represents a challenge. We tested whether a cellular-driven approach could help to identify new modifier genes and especially their mechanism of action. Methods and results: We generated human-induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM) from two patients carrying the same KCNQ1-Y111C mutation, but presenting opposite clinical phenotypes. We showed that the phenotype of the iPSC-CMs derived from the symptomatic patient is due to impaired trafficking and increased degradation of the mutant KCNQ1 and wild-type human ether-a-go-go-related gene. In the iPSC-CMs of the asymptomatic (AS) patient, the activity of an E3 ubiquitin-protein ligase (Nedd4L) involved in channel protein degradation was reduced and resulted in a decreased arrhythmogenic substrate. Two single-nucleotide variants (SNVs) on the Myotubularin-related protein 4 (MTMR4) gene, an interactor of Nedd4L, were identified by whole-exome sequencing as potential contributors to decreased Nedd4L activity. Correction of these SNVs by CRISPR/Cas9 unmasked the LQTS phenotype in AS cells. Importantly, the same MTMR4 variants were present in 77% of AS Y111C mutation carriers of a separate cohort. Thus, genetically mediated interference with Nedd4L activation seems associated with protective effects. Conclusion: Our finding represents the first demonstration of the cellular mechanism of action of a protective modifier gene in LQTS. It provides new clues for advanced risk stratification and paves the way for the design of new therapies targeting this specific molecular pathway.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://cardiovascres.oxfordjournals.org-
dc.relation.ispartofCardiovascular Research-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectLong QT syndrome-
dc.subjectInduced pluripotent stem cells-
dc.subjectArrhythmias-
dc.subjectVariants-
dc.subjectNedd4L-
dc.titleMTMR4 SNVs modulate ion channel degradation and clinical severity in congenital Long QT Syndrome: insights in the mechanism of action of protective modifier genes-
dc.typeArticle-
dc.identifier.emailLee, Y-K: carol801@hku.hk-
dc.identifier.emailMak, TSH: Timothy.Mak@hku.hk-
dc.identifier.emailSham, PC: pcsham@hku.hk-
dc.identifier.emailTse, H-F: hftse@hkucc.hku.hk-
dc.identifier.authorityLee, Y-K=rp02636-
dc.identifier.authoritySham, PC=rp00459-
dc.identifier.authorityTse, H-F=rp00428-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1093/cvr/cvaa019-
dc.identifier.scopuseid_2-s2.0-85102221949-
dc.identifier.hkuros248948-
dc.identifier.hkuros314598-
dc.identifier.volume117-
dc.identifier.issue3-
dc.identifier.spage767-
dc.identifier.epage779-
dc.identifier.isiWOS:000637025500023-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0008-6363-

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