Copy number variation of LINGO1 in familial dystonic tremor

Author:

Alakbarzade Vafa,Iype Thomas,Chioza Barry A.,Singh Royana,Harlalka Gaurav V.,Hardy Holly,Sreekantan-Nair Ajith,Proukakis Christos,Peall Kathryn,Clark Lorraine N.,Caswell Richard,Lango Allen Hana,Wakeling Matthew,Chilton John K.,Baple Emma L.,Louis Elan D.,Warner Thomas T.,Crosby Andrew H.

Abstract

ObjectiveTo elucidate the genetic cause of a large 5 generation South Indian family with multiple individuals with predominantly an upper limb postural tremor and posturing in keeping with another form of tremor, namely, dystonic tremor.MethodsWhole-genome single nucleotide polymorphism (SNP) microarray analysis was undertaken to look for copy number variants in the affected individuals.ResultsWhole-genome SNP microarray studies identified a tandem duplicated genomic segment of chromosome 15q24 present in all affected family members. Whole-genome sequencing demonstrated that it comprised a ∼550-kb tandem duplication encompassing the entire LINGO1 gene.ConclusionsThe identification of a genomic duplication as the likely molecular cause of this condition, resulting in an additional LINGO1 gene copy in affected cases, adds further support for a causal role of this gene in tremor disorders and implicates increased expression levels of LINGO1 as a potential pathogenic mechanism.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Essential Tremor;Movement Disorders Phenomenology;2024

2. Diagnostic Uncertainties in Tremor;Seminars in Neurology;2023-02

3. Dystonia and tremor: Do they have a shared biology?;International Review of Neurobiology;2023

4. Uncovering Essential Tremor Genetics: The Promise of Long-Read Sequencing;Frontiers in Neurology;2022-03-23

5. Is essential tremor a family of diseases or a syndrome? A family of diseases;International Review of Neurobiology;2022

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