Opalka B, Wandl U, Kloke O, Oberle C, Koppe J, Niederle N, Schmidt C G
Department of Internal Medicine, University Essen, FRG.
Blood. 1989 Feb 15;73(3):814-7.
The BCR gene on chromosome 22 has received increasing attention because of its involvement in the Philadelphia (Ph') translocation. For most restriction enzymes, this locus has been found to be nonpolymorphic. Two alleles have only been found when Taql-digested DNA is hybridized to a 5' bcr-specific probe. We describe another two-allele polymorphism detected by the same probe in PvuII-digested DNA. The polymorphism is characterized by an additional PvuII site in the bcr region: this causes the appearance of an additional band of about 2.3 kb or 2.5 kb besides a 4.8-kb fragment in hybridizations with the 5' bcr or a 3' bcr probe. The incidence of the second allele is very low. It has only been found in some patients with hematopoietic malignancies and in a group of volunteers having a leukemia patient in their families.
由于22号染色体上的BCR基因参与了费城(Ph')易位,它受到了越来越多的关注。对于大多数限制酶而言,该基因座已被发现是非多态性的。仅在将经TaqI消化的DNA与5' bcr特异性探针杂交时才发现了两个等位基因。我们描述了在经PvuII消化的DNA中由同一探针检测到的另一种双等位基因多态性。该多态性的特征是bcr区域中存在一个额外的PvuII位点:这导致在与5' bcr或3' bcr探针杂交时,除了4.8 kb的片段外,还出现了一条约2.3 kb或2.5 kb的额外条带。第二个等位基因的发生率非常低。仅在一些造血系统恶性肿瘤患者以及一组家中有白血病患者的志愿者中发现过。