Sack G H, Morrell J C
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Biochem Biophys Res Commun. 1993 Mar 31;191(3):955-60. doi: 10.1006/bbrc.1993.1310.
Adrenoleukodystrophy is a lethal X-linked neurodegenerative disorder which maps close to the red/green color pigment gene cluster in Xq28. We have reported a broad spectrum of color pigment gene changes in adrenoleukodystrophy patients, indicating that the genes may be quite close together. We now have used anonymous DNA probes centromeric to the color pigment gene cluster to analyze patients from 59 adrenoleukodystrophy kindreds. All patients showed normal hybridization using probe Fr9, 30 kb centromeric to the color pigment genes. However, using probe Fr11, 100 kb further centromeric, we found overlapping deletions in 2 patients. We isolated conventional and cosmid genomic clones encompassing 24 kb surrounding Fr11; the clones and map derived from this region localize the telomeric ends of the two deletions to distinct positions 8 kb apart. These overlapping deletions implicate this specific region as a likely site for the ALD gene.
肾上腺脑白质营养不良是一种致命的X连锁神经退行性疾病,其基因定位靠近Xq28的红/绿颜色色素基因簇。我们已报道了肾上腺脑白质营养不良患者中广泛的颜色色素基因变化,表明这些基因可能彼此非常接近。我们现在使用位于颜色色素基因簇着丝粒侧的匿名DNA探针,对来自59个肾上腺脑白质营养不良家族的患者进行分析。所有患者使用位于颜色色素基因着丝粒侧30 kb处的探针Fr9进行杂交时均显示正常。然而,使用位于着丝粒侧再远100 kb处的探针Fr11时,我们在2例患者中发现了重叠缺失。我们分离出了包含围绕Fr11的24 kb的常规基因组克隆和黏粒基因组克隆;从该区域获得的克隆和图谱将两个缺失的端粒末端定位到相距8 kb的不同位置。这些重叠缺失表明该特定区域可能是肾上腺脑白质营养不良(ALD)基因的所在位点。