Vetrie D, Boye E, Flinter F, Bobrow M, Harris A
Paediatric Research Unit, United Medical School, Guy's Hospital, London, United Kingdom.
Genomics. 1992 Nov;14(3):624-33. doi: 10.1016/s0888-7543(05)80161-2.
Alport syndrome (AS), an X-linked kidney disorder, has been shown to be caused by mutations in the gene for the alpha 5-chain of type IV collagen (COL4A5), which maps to Xq22. On the basis of the results of conventional Southern blot analysis of AS patient DNAs, we employed pulsed-field gel electrophoresis to characterize further three gene rearrangements at the 3'-end of alpha 5(IV). We were able to construct long-range restriction maps for all three of these patients and deduce the extent and nature of each rearrangement. One of these mutations is a 450-kb simple deletion that includes 12 kb of the alpha 5(IV) gene. A second mutation has been shown to be a direct duplication of 35 kb of alpha 5(IV) genomic DNA, and a third mutation involves a complex insertion/deletion event resulting in an overall loss of 25 kb.
奥尔波特综合征(AS)是一种X连锁的肾脏疾病,已被证明是由IV型胶原α5链(COL4A5)基因的突变引起的,该基因定位于Xq22。基于对AS患者DNA进行常规Southern印迹分析的结果,我们采用脉冲场凝胶电泳进一步鉴定α5(IV)3'端的三种基因重排。我们能够构建这三位患者的长距离限制性图谱,并推断出每种重排的范围和性质。其中一种突变是450kb的简单缺失,包括12kb的α5(IV)基因。第二种突变已被证明是35kb的α5(IV)基因组DNA的直接重复,第三种突变涉及复杂的插入/缺失事件,导致总共丢失25kb。