Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi Y K, Arahata K, Nonaka I, Hirai S
National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278.
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.
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。