Wapenaar M C, Petit C, Basler E, Ballabio A, Henke A, Rappold G A, van Paassen H M, Blonden L A, van Ommen G J
Department of Human Genetics, Sylvius Laboratory, Leiden University, The Netherlands.
Genomics. 1992 May;13(1):167-75. doi: 10.1016/0888-7543(92)90217-g.
We have isolated 14 new DNA markers from the human Xpter-Xp21 region distal to the Duchenne muscular dystrophy gene by targeted cloning, employing two somatic cell hybrids containing this region as their sole human material. High-resolution physical localization of these markers within this region was obtained by hybridization to two mapping panels consisting of DNA from patients carrying various translocations and deletions in distal Xp. Five markers were assigned to the pseudoautosomal region where their position on the long-range map of this region was further determined by pulsed-field gel electrophoresis. The other nine markers map to the X-specific region. Informative TaqI restriction fragment length polymorphisms were observed for four loci. One of these represents a region-specific low-copy repeated element. These 14 new markers represent useful tools for the understanding of distal Xp deletion and translocation mechanisms and for the positional cloning of disease genes in the region.
我们通过靶向克隆,从杜兴氏肌营养不良基因远端的人类Xpter-Xp21区域分离出了14个新的DNA标记,采用了两个体细胞杂种,它们仅含该区域作为其唯一的人类材料。通过与两个由携带远端Xp各种易位和缺失的患者DNA组成的定位板杂交,获得了这些标记在该区域内的高分辨率物理定位。五个标记被定位到假常染色体区域,通过脉冲场凝胶电泳进一步确定了它们在该区域长程图谱上的位置。其他九个标记定位于X特异性区域。在四个位点观察到了有信息的TaqI限制性片段长度多态性。其中一个代表区域特异性低拷贝重复元件。这14个新标记是理解远端Xp缺失和易位机制以及该区域疾病基因定位克隆的有用工具。