首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues.
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A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues.

机译:71千达尔顿蛋白是大脑和其他非肌肉组织中Duchenne肌肉营养不良基因的主要产物。

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摘要

The known Duchenne muscular dystrophy (DMD) gene products, the muscle- and brain-type dystrophin isoforms, are 427-kDa proteins translated from 14-kilobase (kb) mRNAs. Recently we described a 6.5-kb mRNA that also is transcribed from the DMD gene. Cloning and in vitro transcription and translation of the entire coding region show that the 6.5-kb mRNA encodes a 70.8-kDa protein that is a major product of the DMD gene. It contains the C-terminal and the cysteine-rich domains of dystrophin, seven additional amino acids at the N terminus, and some modifications formed by alternative splicing in the C-terminal domain. It lacks the entire large domain of spectrin-like repeats and the actin-binding N-terminal domain of dystrophin. This protein is the major DMD gene product in brain and other nonmuscle tissues but is undetectable in skeletal muscle extracts.
机译:已知的Duchenne肌肉营养不良(DMD)基因产物,即肌肉和脑型肌营养不良蛋白亚型,是从14碱基(kb)mRNA翻译而来的427 kDa蛋白。最近,我们描述了也从DMD基因转录的6.5-kb mRNA。整个编码区的克隆以及体外转录和翻译显示,6.5-kb mRNA编码70.8-kDa蛋白,该蛋白是DMD基因的主要产物。它包含肌营养不良蛋白的C末端和富含半胱氨酸的结构域,N末端的七个额外氨基酸以及在C末端结构域中通过可变剪接形成的一些修饰。它缺乏血影蛋白样重复序列的整个大结构域和肌营养不良蛋白的肌动蛋白结合N末端结构域。该蛋白是大脑和其他非肌肉组织中主要的DMD基因产物,但在骨骼肌提取物中却无法检测到。

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