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日本的先天性肌无力综合征:肌肉烟碱型乙酰胆碱受体亚基的种族特异性突变

Congenital myasthenic syndrome in Japan: ethnically unique mutations in muscle nicotinic acetylcholine receptor subunits.

作者信息

Azuma Yoshiteru, Nakata Tomohiko, Tanaka Motoki, Shen Xin-Ming, Ito Mikako, Iwata Satoshi, Okuno Tatsuya, Nomura Yoshiko, Ando Naoki, Ishigaki Keiko, Ohkawara Bisei, Masuda Akio, Natsume Jun, Kojima Seiji, Sokabe Masahiro, Ohno Kinji

机构信息

Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Department of Physiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Neuromuscul Disord. 2015 Jan;25(1):60-9. doi: 10.1016/j.nmd.2014.09.002. Epub 2014 Sep 10.

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.

摘要

先天性肌无力综合征(CMS)由神经肌肉接头处表达的基因突变引起。大多数CMS患者来自西方国家和中东地区,日本仅报告过4例COLQ基因突变患者。我们在此报告了5例日本患者乙酰胆碱受体(AChR)亚基基因中的6种突变。其中5种突变为新发现的突变,1种突变与一名欧美患者相同,但单倍型不同。在观察到的突变中,ε亚基中的p.Thr284Pro(根据旧注释为p.Thr264Pro)导致慢通道CMS。δ和ε亚基中的其他5种突变是剪接位点、移码、无效或错义突变,导致终板AChR缺乏。我们还在另一名患者的β亚基中发现了杂合的p.Met465Thr。然而,p.Met465Thr可能是一种多态性,因为单通道记录显示通道开放轻度缩短,但不影响AChR的细胞表面表达,并且p.Met465Thr在日本人群中的次要等位基因频率为5.1%。日本患者与其他患者之间缺乏共享的突变等位基因,这表明这里描述的大多数突变在种族上是独特的,或者在每个家族中是新发的。

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