Burmeister M, Lehrach H
Nature. 1986;324(6097):582-5. doi: 10.1038/324582a0.
Duchenne muscular dystrophy is an X-linked recessive disease affecting about 1 in 4,000 newborn boys. As in many other inherited diseases, the biochemical basis of the condition is unknown, and as yet there is no effective treatment. Translocations, deletions and other mutations leading to the DMD phenotype are distributed over a chromosomal area of large, but unknown size. Using pulsed-field gradient gel electrophoresis, we have now determined restriction maps of a major fraction of this area, covering two regions of three million basepairs in total, and used it to determine the position of several probes linked to DMD. The maps establish physical distances between structural changes associated with the DMD phenotype and provide evidence for a CpG-rich island proximal to the area containing translocations and deletions associated with the DMD phenotype.
杜氏肌营养不良症是一种X连锁隐性疾病,每4000名新生男婴中约有1人患病。与许多其他遗传性疾病一样,该病的生化基础尚不清楚,目前也没有有效的治疗方法。导致杜氏肌营养不良症(DMD)表型的易位、缺失和其他突变分布在一个大小未知但很大的染色体区域。我们现在利用脉冲场梯度凝胶电泳确定了该区域大部分区域的限制性图谱,总共覆盖了两个三百万碱基对的区域,并利用它来确定几个与DMD相关的探针的位置。这些图谱确定了与DMD表型相关的结构变化之间的物理距离,并为靠近包含与DMD表型相关的易位和缺失区域的富含CpG的岛提供了证据。