Chen W, Butler M, Rao P H, Chaganti S R, Louie D C, Dalla-Favera R, Chaganti R S
Department of Human Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Oncogene. 1998 Oct 1;17(13):1717-22. doi: 10.1038/sj.onc.1202098.
The BCL6 gene, mapped at the chromosomal band 3q27, encodes a POZ/Zinc finger transcription repressor protein. It is frequently activated in Non-Hodgkin's lymphomas (NHL) by translocations with breakpoints clustering in the 5' major breakpoint region (MBR) as well as by mutations in the same region. The translocations lead to BCL6 activation by substitution of promoters of rearranging genes derived from the reciprocal chromosomal partners such as IG. We report the molecular genetic analysis of a novel t(2;3)(q21;q27) translocation subset in NHL comprising three cases without apparent BCL6 involvement in the translocation. Southern blot analysis of tumor DNAs utilizing BCL6 MBR probes revealed no rearrangement in two cases. Two rearranged bands in the third case resulted from a deletion in one allele and a mutation in the other allele. Southern blot analysis of DNA from one of the two tumors without BCL6 rearrangement, using a probe derived from the recently identified alternative breakpoint region (ABR), showed a rearrangement. The ABR is located 200-270 kb telomeric to MBR. Mutations were identified in the previously reported hypermutable region of BCL6 in all three tumors. In one, the mutant allele alone was found to be expressed by RT-PCR analysis of RNA. These results demonstrate the presence of 3q27 translocation breakpoints at a distance from BCL6 suggesting distant breaks that deregulate the gene or involvement of other genes that may be subject to rearrangement.
BCL6基因定位于染色体3q27带,编码一种POZ/锌指转录抑制蛋白。在非霍奇金淋巴瘤(NHL)中,它常通过与5'主要断裂点区域(MBR)聚集的断裂点发生易位以及同一区域的突变而被激活。这些易位通过替换来自相互染色体伙伴(如IG)的重排基因的启动子导致BCL6激活。我们报告了NHL中一个新的t(2;3)(q21;q27)易位子集的分子遗传学分析,该子集包含3例在易位中无明显BCL6参与的病例。利用BCL6 MBR探针对肿瘤DNA进行Southern印迹分析,发现2例无重排。第三例中的两条重排带是由一个等位基因的缺失和另一个等位基因的突变导致的。使用来自最近鉴定的替代断裂点区域(ABR)的探针,对两个无BCL6重排的肿瘤之一的DNA进行Southern印迹分析,显示有重排。ABR位于MBR端粒200 - 270 kb处。在所有三个肿瘤中,均在先前报道的BCL6高变区发现了突变。在其中一个肿瘤中,通过对RNA进行RT-PCR分析发现仅突变等位基因有表达。这些结果表明在距离BCL6一定距离处存在3q27易位断裂点,提示存在远距离断裂从而使该基因失调或其他可能发生重排的基因参与其中。