End-plate acetylcholine receptor deficiency due to nonsense mutations in the ε subunit

Andrew G Engel, Kinji Ohno, Cecilia Bouzat, Steven M Sine, Robert C. Griggs

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120 Citations (Scopus)

Abstract

We describe a congenital myasthenic syndrome associated with severe end- plate (EP) acetylcholine receptor (AChR) deficiency not associated with an EP myopathy, and with evidence of immature AChR, containing the γ instead of the ε subunit (γ-AChR) at the EPs. Molecular genetic analysis of AChR- subunit genes revealed two mutations in the ε-subunit gene: insertion of a thymine after ε nucleotide 1101 (ε1101insT) that generates a nonsense codon directly, and insertion of a guanine after ε nucleotide 1293 (ε1293insG) that generates three missense codons followed by a nonsense codon. Each mutation predicts truncation of the ε subunit at the level of the long cytoplasmic loop, between the third (M3) and fourth (M4) membrane spanning domains. The propositus' asymptomatic son carries ε1293G, indicating that the two mutations are heteroallelic. Expression of AChR harboring either mutation in human embryonic kidney (HEK) fibroblasts was markedly reduced. Single-channel activity recorded from HEK cells expressing ε1101insT-AChR was infrequent but resembled activity of wild-type AChR channels in amplitude and open duration. No channel activity could be recorded from HEK cells expressing ε1293insG-AChR. Expression of γ-AChR at the EPs may serve as the means of phenotypic rescue from potentially fatal nonsense mutations in the ε-subunit gene.

Original languageEnglish (US)
Pages (from-to)810-817
Number of pages8
JournalAnnals of Neurology
Volume40
Issue number5
StatePublished - Nov 1996

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Nonsense Codon
Cholinergic Receptors
Mutation
Kidney
Thymine Nucleotides
Congenital Myasthenic Syndromes
Guanine Nucleotides
Insertional Mutagenesis
Muscular Diseases
Human Activities
Codon
Genes
Molecular Biology
Fibroblasts
Membranes

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

End-plate acetylcholine receptor deficiency due to nonsense mutations in the ε subunit. / Engel, Andrew G; Ohno, Kinji; Bouzat, Cecilia; Sine, Steven M; Griggs, Robert C.

In: Annals of Neurology, Vol. 40, No. 5, 11.1996, p. 810-817.

Research output: Contribution to journalArticle

Engel, Andrew G ; Ohno, Kinji ; Bouzat, Cecilia ; Sine, Steven M ; Griggs, Robert C. / End-plate acetylcholine receptor deficiency due to nonsense mutations in the ε subunit. In: Annals of Neurology. 1996 ; Vol. 40, No. 5. pp. 810-817.
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