van Deutekom J C, Wijmenga C, van Tienhoven E A, Gruter A M, Hewitt J E, Padberg G W, van Ommen G J, Hofker M H, Frants R R
MGC-Department of Human Genetics, Leiden University, The Netherlands.
Hum Mol Genet. 1993 Dec;2(12):2037-42. doi: 10.1093/hmg/2.12.2037.
Facioscapulohumeral muscular dystrophy (FSHD) is a neuromuscular disorder characterized by progressive weakness of the facial, shoulder and upper arm muscles. The disease is associated with DNA rearrangements which are detectable using probe p13E-11 (D4F104S1) in DNA digested with EcoRI or other restriction enzymes. We have cloned and characterized the rearranged EcoRI fragment of four unrelated FSHD patients. Restriction fragment mapping and DNA sequence analysis showed that the proximal and distal parts of the EcoRI fragment, which flank a region of tandemly repeated 3.2 kb units, are identical in normal and rearranged EcoRI fragments. These results strongly support the hypothesis that the FSHD associated rearrangements are due to deletions of integral copies of the 3.2 kb repeated unit. Since these repeated units are likely to form part of the FSHD transcription unit, the variation in repeat unit number might affect the function of the gene product. Hence, our data confine the FSHD gene region and thus provide a starting point for cloning the FSHD gene.
面肩肱型肌营养不良症(FSHD)是一种神经肌肉疾病,其特征为面部、肩部和上臂肌肉进行性无力。该疾病与DNA重排有关,在用EcoRI或其他限制性酶消化的DNA中,使用探针p13E - 11(D4F104S1)可检测到这种重排。我们克隆并鉴定了4名无亲缘关系的FSHD患者的重排EcoRI片段。限制性片段图谱分析和DNA序列分析表明,EcoRI片段的近端和远端部分位于串联重复的3.2 kb单位区域两侧,在正常和重排的EcoRI片段中是相同的。这些结果有力地支持了以下假说:FSHD相关的重排是由于3.2 kb重复单位的完整拷贝缺失所致。由于这些重复单位可能构成FSHD转录单位的一部分,重复单位数量的变化可能会影响基因产物的功能。因此,我们的数据确定了FSHD基因区域,从而为克隆FSHD基因提供了一个起点。