Buiting K, Dittrich B, Robinson W P, Guitart M, Abeliovich D, Lerer I, Horsthemke B
Institut für Humangenetik, Universitätsklinikum Essen, Germany.
Hum Mol Genet. 1994 Jun;3(6):893-5. doi: 10.1093/hmg/3.6.893.
Most patients with Prader-Willi syndrome have a deletion of 15q11-13 or maternal uniparental disomy for chromosome 15. The shortest region of deletion overlap is presently defined by the gene for the small nuclear ribonucleoprotein N (SNRPN). We have investigated the integrity of SNRPN as well as the methylation status of D15S63 (PW71) in two patients with apparently normal chromosomes 15 of biparental origin. SNRPN is normal in one patient and deleted in the other one. Both patients are intact at the D15S63 locus, but have an abnormal methylation pattern. These results suggest that a DNA sequence close to SNRPN determines the methylation status of D15S63 and that the methylation test does not only detect the common deletions and uniparental disomy, but other rare lesions as well.
大多数普拉德-威利综合征患者存在15q11 - 13缺失或15号染色体的母源单亲二体。目前,缺失重叠的最短区域由小核核糖核蛋白N(SNRPN)基因定义。我们研究了两名双亲来源的15号染色体看似正常的患者中SNRPN的完整性以及D15S63(PW71)的甲基化状态。一名患者的SNRPN正常,另一名患者的SNRPN缺失。两名患者在D15S63位点均完整,但甲基化模式异常。这些结果表明,靠近SNRPN的DNA序列决定了D15S63的甲基化状态,并且甲基化检测不仅能检测常见的缺失和单亲二体,还能检测其他罕见病变。