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A frameshifting 7 bp deletion (ε553del7) in exon 7 of  CHRNE  encoding the acetylcholine receptor ε subunit, observed in seven congenital myasthenic syndrome patients, enhances expression of an aberrantly spliced transcript that skips the preceding 101 bp exon 6. To recapitulate the aberrant splicing, we cloned the entire  CHRNE  spanning 12 exons and 11 introns and expressed it in COS cells. Scanning mutagenesis revealed that ε553del7 does not disrupt an exonic splicing enhancer. Inhibition of protein synthesis and of nonsense-mediated mRNA decay (NMD) by anisomycin shows that even wild-type  CHRNE  produces an exon 6-skipped transcript, and that even ε553del7- CHRNE  yields a normally spliced transcript. Both transcripts, however, are degraded by NMD due to a premature stop codon. In contrast, the normally spliced transcript from wild-type  CHRNE  and the exon 6-skipped transcript from ε553del7- CHRNE  carry no premature stop codon and hence are immune to NMD. Optimization of splicing signals for exon 6 prevents it being skipped even in the presence of anisomycin and/or ε553del7, indicating that inherently weak splicing signals for exon 6 account for its skipping. We suggest that a similar mechanism probably operates in other genes in skipping of remote exons. The presence of weak splicing signals for exon 6 also prompted us to search for mutations in exon 6 that disrupt an exonic splicing enhancer. Indeed, we found that εEF157V and εE154X in exon 6, observed in two other patients, caused aberrant splicing of exon 6.

A frameshifting mutation in CHRNE unmasks skipping of the preceding exon