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抗肌萎缩蛋白在神经肌肉疾病中的蛋白表达

Telethonin protein expression in neuromuscular disorders.

作者信息

Vainzof Mariz, Moreira Eloisa S, Suzuki Oscar T, Faulkner Georgine, Valle Georgio, Beggs Alan H, Carpen Olli, Ribeiro Alberto F, Zanoteli Edmar, Gurgel-Gianneti Juliana, Tsanaclis Ana Maria, Silva Helga C A, Passos-Bueno Maria Rita, Zatz Mayana

机构信息

Center for the Study of the Human Genome, Department Biology, IBUSP, University of Sao Paulo, R. do Matão, 277, sala 220-Cidade Universitária, São Paulo, Brazil.

出版信息

Biochim Biophys Acta. 2002 Oct 9;1588(1):33-40. doi: 10.1016/s0925-4439(02)00113-8.

Abstract

Telethonin is a 19-kDa sarcomeric protein, localized to the Z-disc of skeletal and cardiac muscles. Mutations in the telethonin gene cause limb-girdle muscular dystrophy type 2G (LGMD2G). We investigated the sarcomeric integrity of muscle fibers in LGMD2G patients, through double immunofluorescence analysis for telethonin with three sarcomeric proteins: titin, alpha-actinin-2, and myotilin and observed the typical cross striation pattern, suggesting that the Z-line of the sarcomere is apparently preserved, despite the absence of telethonin. Ultrastructural analysis confirmed the integrity of the sarcomeric architecture. The possible interaction of telethonin with other proteins responsible for several forms of neuromuscular disorders was also analyzed. Telethonin was clearly present in the rods in nemaline myopathy (NM) muscle fibers, confirming its localization to the Z-line of the sarcomere. Muscle from patients with absent telethonin showed normal expression for the proteins dystrophin, sarcoglycans, dysferlin, and calpain-3. Additionally, telethonin showed normal localization in muscle biopsies from patients with LGMD2A, LGMD2B, sarcoglycanopathies, and Duchenne muscular dystrophy (DMD). Therefore, the primary deficiency of calpain-3, dysferlin, sarcoglycans, and dystrophin do not seem to alter telethonin expression.

摘要

肌联蛋白是一种19 kDa的肌节蛋白,定位于骨骼肌和心肌的Z线。肌联蛋白基因突变会导致2G型肢带型肌营养不良(LGMD2G)。我们通过对肌联蛋白与三种肌节蛋白(肌联蛋白、α-辅肌动蛋白-2和肌联蛋白)进行双重免疫荧光分析,研究了LGMD2G患者肌肉纤维的肌节完整性,并观察到典型的横纹模式,这表明尽管缺乏肌联蛋白,但肌节的Z线显然是保留的。超微结构分析证实了肌节结构的完整性。我们还分析了肌联蛋白与其他导致多种形式神经肌肉疾病的蛋白质之间可能的相互作用。在杆状肌病(NM)肌肉纤维的杆状体中明显存在肌联蛋白,这证实了它定位于肌节的Z线。缺乏肌联蛋白的患者的肌肉中,抗肌萎缩蛋白、肌聚糖、肌膜蛋白和钙蛋白酶-3的表达正常。此外,在LGMD2A、LGMD2B、肌聚糖病和杜兴氏肌营养不良(DMD)患者的肌肉活检中,肌联蛋白的定位正常。因此,钙蛋白酶-3、肌膜蛋白、肌聚糖和抗肌萎缩蛋白的原发性缺陷似乎不会改变肌联蛋白的表达。

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