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严重儿童常染色体隐性遗传性肌营养不良症肌肉中肌聚糖复合物的选择性缺陷

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.

作者信息

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi Y K, Arahata K, Nonaka I, Hirai S

机构信息

National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278.

Abstract

Dystrophin-associated glycoprotein complex is classified into two subcomplexes: the dystroglycan complex (156DAG and 43DAG) and the sarcoglycan complex (50DAG, A3b, and 35DAG). Severe childhood autosomal recessive muscular dystrophy (SCARMD) was first reported to result from a deficiency of 50DAG. We examined muscles from five SCARMD patients and found that dystrophin and 43DAG were present in almost normal levels while 35DAG and the newly-identified protein A3b in addition to 50DAG were absent or greatly reduced. Therefore, SCARMD is the disease with a selective defect of the sarcoglycan complex.

摘要

肌营养不良蛋白相关糖蛋白复合体分为两个亚复合体

肌营养不良聚糖复合体(156DAG和43DAG)和肌糖蛋白复合体(50DAG、A3b和35DAG)。重度儿童常染色体隐性遗传性肌营养不良症(SCARMD)首次报道是由于50DAG缺乏所致。我们检查了5例SCARMD患者的肌肉,发现肌营养不良蛋白和43DAG水平几乎正常,而35DAG以及新发现的蛋白A3b连同50DAG缺失或大幅减少。因此,SCARMD是一种肌糖蛋白复合体存在选择性缺陷的疾病。

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