Nakamura Y, Miki T, Miura I, Hashimoto K, Miura A, Akimoto K, Hirosawa S, Saito K, Enokihara H, Furusawa S, Shishido H
Third Department of Internal Medicine, Dokkyo University School of Medicine, Tochigi, Japan.
Leukemia. 1996 Apr;10(4):658-61.
Chromosomal translocations involving the band 3q27 are recognized as common specific cytogenetic abnormalities in B cell non-Hodgkin's lymphoma (NHL), and the BCL-6 gene, identified on 3q27 was shown to be disrupted by these translocations. Previously, we have reported biallelic BCL-6 rearrangements occurring in some patients with B cell NHL. In the present study, we describe a NHL patient with t(3;22)(q27;q11) translocation. In this patient, biallelic BCL-6 abnormalities were indicated by Southern blot analysis. Further studies revealed that one of the two independent abnormalities was a juxtaposition to the immunoglobulin (Ig) lambda gene associated with chromosomal translocation, whereas the other was an internal DNA deletion of 1.5 kb area on untranslocated chromosome 3. Deletion junctions were located within the first exon and the 5' region of the first intron. The result provides the evidence that, besides chromosomal translocation, submicroscopic local DNA recombination can cause structural alteration of the BCL-6 gene.
涉及3q27带的染色体易位被认为是B细胞非霍奇金淋巴瘤(NHL)常见的特异性细胞遗传学异常,并且在3q27上鉴定出的BCL-6基因被证明会因这些易位而中断。此前,我们报道了一些B细胞NHL患者中发生的双等位基因BCL-6重排。在本研究中,我们描述了一名患有t(3;22)(q27;q11)易位的NHL患者。在该患者中,Southern印迹分析表明存在双等位基因BCL-6异常。进一步研究显示,两个独立异常中的一个是与染色体易位相关的免疫球蛋白(Ig)λ基因并列,而另一个是未易位的3号染色体上1.5 kb区域的内部DNA缺失。缺失连接点位于第一个外显子和第一个内含子的5'区域内。该结果提供了证据,表明除染色体易位外,亚显微局部DNA重组可导致BCL-6基因的结构改变。