| Literature DB >> 25264167 |
Yoshiteru Azuma1, Tomohiko Nakata1, Motoki Tanaka2, Xin-Ming Shen3, Mikako Ito4, Satoshi Iwata4, Tatsuya Okuno4, Yoshiko Nomura5, Naoki Ando6, Keiko Ishigaki7, Bisei Ohkawara4, Akio Masuda4, Jun Natsume8, Seiji Kojima8, Masahiro Sokabe2, Kinji Ohno9.
Abstract
Congenital myasthenic syndromes (CMS) are caused by mutations in genes expressed at the neuromuscular junction. Most CMS patients have been reported in Western and Middle Eastern countries, and only four patients with COLQ mutations have been reported in Japan. We here report six mutations in acetylcholine receptor (AChR) subunit genes in five Japanese patients. Five mutations are novel, and one mutation is shared with a European American patient but with a different haplotype. Among the observed mutations, p.Thr284Pro (p.Thr264Pro according to the legacy annotation) in the epsilon subunit causes a slow-channel CMS. Five other mutations in the delta and epsilon subunits are splice site, frameshift, null, or missense mutations causing endplate AChR deficiency. We also found a heteroallelic p.Met465Thr in the beta subunit in another patient. p.Met465Thr, however, was likely to be polymorphism, because single channel recordings showed mild shortening of channel openings without affecting cell surface expression of AChR, and the minor allelic frequency of p.Met465Thr was 5.1% in the Japanese population. Lack of shared mutant alleles between the Japanese and the other patients suggests that most mutations described here are ethnically unique or de novo in each family.Entities:
Keywords: Acetylcholine receptor; Congenital myasthenic syndromes; Endplate acetylcholine receptor deficiency; Fast channel syndrome; Slow channel syndrome
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Year: 2014 PMID: 25264167 DOI: 10.1016/j.nmd.2014.09.002
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296