Feil R, Aubourg P, Mosser J, Douar A M, Le Paslier D, Philippe C, Mandel J L
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Strasbourg, France.
Am J Hum Genet. 1991 Dec;49(6):1361-71.
We have characterized a complex chromosomal rearrangement in band Xq28, in an adrenoleukodystrophy patient who also has blue-cone monochromacy. A 130-kb region upstream from the color-vision pigment genes was isolated as yeast artificial chromosome or cosmid clones. Another Xq28 sequence, not included in the above region, was obtained by cloning a deletion breakpoint from the patient. Using probes derived from the cloned sequences, we have shown that the rearrangement affects the color-pigment genes and includes two deletions, most likely separated by a large (greater than 110-kb) inversion. One deletion encompasses part of the pigment gene cluster and 33 kb of upstream sequences and accounts for the patient's blue-cone monochromacy. If this rearrangement also caused ALD, the disease gene would be expected to lie within or close to one of the deletions. However, deletions were not detected in a 50-kb region upstream of the red-color-pigment gene in 81 other ALD patients. Two CpG islands were mapped, at 46 and 115 kb upstream from the pigment genes.
我们在一名同时患有蓝锥单色视的肾上腺脑白质营养不良患者中,对Xq28带的复杂染色体重排进行了特征分析。从色觉色素基因上游130 kb的区域分离出酵母人工染色体或黏粒克隆。通过克隆该患者的一个缺失断点,获得了上述区域未包含的另一个Xq28序列。利用从克隆序列衍生的探针,我们发现该重排影响色素基因,包括两个缺失,很可能由一个大的(大于110 kb)倒位隔开。一个缺失包含部分色素基因簇和33 kb的上游序列,这解释了患者的蓝锥单色视。如果这种重排也导致了肾上腺脑白质营养不良,那么疾病基因预计位于其中一个缺失内或附近。然而,在其他81名肾上腺脑白质营养不良患者的红色素基因上游50 kb区域未检测到缺失。在色素基因上游46 kb和115 kb处定位了两个CpG岛。