Timms K M, Huckett L E, Belmont J W, Shapira S K, Gibbs R A
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
Hum Mutat. 1998;11(2):121-6. doi: 10.1002/(SICI)1098-1004(1998)11:2<121::AID-HUMU4>3.0.CO;2-M.
Deficiency of the enzyme iduronate-2-sulfatase (IDS) results in Hunter syndrome, an X-linked recessive lysosomal storage disorder. In this study, analysis of a patient with features of moderate to severe Hunter syndrome identified a 178-bp deletion upstream of IDS exon 1 spanning a predicted promoter element. Sequencing of all nine IDS exons from this patient failed to identify any additional mutations within the coding regions or in intron-exon boundaries. The 178-bp deletion is flanked by two 13-bp direct repeats and potential DNA topoisomerase II recognition sites. These findings point toward nonhomologous recombination as a possible mechanism for this mutation. Expression studies on this patient do not detect any IDS transcripts, indicating that the deletion spans sequences essential for IDS expression. Complete lack of expression of IDS is consistent with the moderate to severe phenotype observed in this patient.
艾杜糖醛酸-2-硫酸酯酶(IDS)缺乏会导致亨特综合征,这是一种X连锁隐性溶酶体贮积症。在本研究中,对一名具有中度至重度亨特综合征特征的患者进行分析,发现在IDS外显子1上游有一个178 bp的缺失,该缺失跨越一个预测的启动子元件。对该患者所有9个IDS外显子进行测序,未能在编码区或内含子-外显子边界发现任何其他突变。178 bp的缺失两侧是两个13 bp的直接重复序列和潜在的DNA拓扑异构酶II识别位点。这些发现表明非同源重组可能是该突变的机制。对该患者的表达研究未检测到任何IDS转录本,表明该缺失跨越了IDS表达所必需的序列。IDS完全缺乏表达与该患者观察到的中度至重度表型一致。