Blake D J, Love D R, Tinsley J, Morris G E, Turley H, Gatter K, Dickson G, Edwards Y H, Davies K E
Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
Hum Mol Genet. 1992 May;1(2):103-9. doi: 10.1093/hmg/1.2.103.
The 14kb dystrophin transcript from the Duchenne muscular dystrophy (DMD) locus, which encodes a 427kDa protein, is differentially spliced at the amino terminal end giving rise to alternative transcripts expressed in muscle and brain. Here we present evidence for a 4.8kb transcript from the DMD locus which is ubiquitously expressed but is particularly abundant in Schwannoma cells where dystrophin could not be detected. The hybridisation of Western blots with dystrophin antibodies also identifies a protein of approximately 80kDa of variable abundance in different human and mdx tissues. Immunocytochemistry studies confirm the expression of this protein in nerve cells, a tissue in which full length dystrophin is not detected. Sequencing of the 5' end of a clone isolated from a rat Schwannoma cDNA library, shows that the 4.8kb transcript shares exons with the carboxy terminal end of dystrophin but the 5' untranslated region is not contained within the dystrophin transcript. We propose that the 4.8kb gene product be called apodystrophin-1 as its expression is distinct from the dystrophin 14kb mRNA but it is transcribed from the same locus.
来自杜兴氏肌营养不良症(DMD)基因座的14kb抗肌萎缩蛋白转录本,编码一种427kDa的蛋白质,在氨基末端进行差异剪接,产生在肌肉和大脑中表达的可变转录本。在此,我们提供证据表明,来自DMD基因座的一个4.8kb转录本在各处均有表达,但在未检测到抗肌萎缩蛋白的神经鞘瘤细胞中尤为丰富。用抗肌萎缩蛋白抗体进行的蛋白质印迹杂交还鉴定出一种约80kDa的蛋白质,其在不同的人类和mdx组织中的丰度各异。免疫细胞化学研究证实了这种蛋白质在神经细胞中的表达,而在该组织中未检测到全长抗肌萎缩蛋白。对从大鼠神经鞘瘤cDNA文库中分离出的一个克隆的5'端进行测序,结果显示,该4.8kb转录本与抗肌萎缩蛋白的羧基末端共有外显子,但5'非翻译区并不包含在抗肌萎缩蛋白转录本内。我们建议将该4.8kb基因产物命名为载脂蛋白抗肌萎缩蛋白-1,因为它的表达不同于14kb的抗肌萎缩蛋白mRNA,但它是从同一基因座转录而来的。