Large genomic deletions in CACNA1A cause episodic ataxia type 2

Jijun Wan, Hafsa Mamsa, Janine L. Johnston, Elizabeth L. Spriggs, Harvey Singer, David Samuel Zee, Alhamza R. Al-Bayati, Robert W. Baloh, Joanna C. Jen

Research output: Contribution to journalArticle

Abstract

Episodic ataxia (EA) syndromes are heritable diseases characterized by dramatic episodes of imbalance and incoordination. EA type 2 (EA2), the most common and the best characterized subtype, is caused by mostly nonsense, splice site, small indel, and sometimes missense mutations in CACNA1A. Direct sequencing of CACNA1A fails to identify mutations in some patients with EA2-like features, possibly due to incomplete interrogation of CACNA1A or defects in other EA genes not yet defined. Previous reports described genomic deletions between 4 and 40 kb in EA2. In 47 subjects with EA (26 with EA2-like features) who tested negative for mutations in the known EA genes, we used multiplex ligation-dependent probe amplification to analyze CACNA1A for exonic copy number variations. Breakpoints were further defined by long-range PCR.We identified distinct multiexonic deletions in three probands with classic EA2-like features: episodes of prolonged vertigo and ataxia triggered by stress and fatigue, interictal nystagmus, with onset during infancy or early childhood. The breakpoints in all three probands are located in Alu sequences, indicating errors in homologous recombination of Alu sequences as the underlying mechanism.The smallest deletion spanned exons 39 and 40, while the largest deletion spanned 200 kb, missing all but the first three exons. One deletion involving exons 39 through 47 arose spontaneously. The search for mutations in CACNA1A appears most fruitful in EA patients with interictal nystagmus and onset early in life. The finding of large heterozygous deletions suggests haploinsufficiency as a possible pathomechanism of EA2.

Original languageEnglish (US)
Article numberArticle 51
JournalFrontiers in Neurology
VolumeSEP
DOIs
StatePublished - 2011

Fingerprint

Exons
Ataxia
Mutation
Haploinsufficiency
Homologous Recombination
Multiplex Polymerase Chain Reaction
Vertigo
Missense Mutation
Genes
Fatigue
Type 2 Episodic Ataxia
Episodic Ataxia
Polymerase Chain Reaction

Keywords

  • CACNA1A
  • EA2
  • Episodic ataxia
  • Genomic rearrangement
  • Mutation

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Large genomic deletions in CACNA1A cause episodic ataxia type 2. / Wan, Jijun; Mamsa, Hafsa; Johnston, Janine L.; Spriggs, Elizabeth L.; Singer, Harvey; Zee, David Samuel; Al-Bayati, Alhamza R.; Baloh, Robert W.; Jen, Joanna C.

In: Frontiers in Neurology, Vol. SEP, Article 51, 2011.

Research output: Contribution to journalArticle

Wan, J, Mamsa, H, Johnston, JL, Spriggs, EL, Singer, H, Zee, DS, Al-Bayati, AR, Baloh, RW & Jen, JC 2011, 'Large genomic deletions in CACNA1A cause episodic ataxia type 2', Frontiers in Neurology, vol. SEP, Article 51. https://doi.org/10.3389/fneur.2011.00051
Wan, Jijun ; Mamsa, Hafsa ; Johnston, Janine L. ; Spriggs, Elizabeth L. ; Singer, Harvey ; Zee, David Samuel ; Al-Bayati, Alhamza R. ; Baloh, Robert W. ; Jen, Joanna C. / Large genomic deletions in CACNA1A cause episodic ataxia type 2. In: Frontiers in Neurology. 2011 ; Vol. SEP.
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