Boye E, Vetrie D, Flinter F, Buckle B, Pihlajaniemi T, Hamalainen E R, Myers J C, Bobrow M, Harris A
Division of Medical and Molecular Genetics, United Medical School, Guy's Hospital, London, United Kingdom.
Genomics. 1991 Dec;11(4):1125-32. doi: 10.1016/0888-7543(91)90040-l.
The gene coding for the alpha 5 chian of type IV collagen (alpha 5(IV) collagen), which maps to Xq22, is a candidate gene for the X-linked dominant disease Alport syndrome (AS). Using three cDNA clones, covering the 3' end of the alpha 5(IV) collagen gene, 3 of 38 patients have been identified with mutations in this gene. Each of these patients shows a gross rearrangement of DNA: a deletion of at least 35 kb, an insertion/deletion event involving approximately 25 kb, and a duplication of at least 35 kb of DNA.
编码IV型胶原α5链(α5(IV)胶原)的基因定位于Xq22,是X连锁显性疾病阿尔波特综合征(AS)的候选基因。利用三个覆盖α5(IV)胶原基因3'端的cDNA克隆,在38例患者中发现3例该基因存在突变。这些患者均出现DNA的大片段重排:至少35kb的缺失、涉及约25kb的插入/缺失事件以及至少35kb的DNA重复。