Dyomin V G, Rao P H, Dalla-Favera R, Chaganti R S
Cell Biology Program and the Department of Human Genetics, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 1997 May 27;94(11):5728-32. doi: 10.1073/pnas.94.11.5728.
Translocations affecting the chromosomal region 15q11-13 and various other partners are recurrent in diffuse large-cell lymphomas (DLCL). To identify the putative gene, here named BCL8, involved in these translocations we have cloned the breakpoint region from a DLCL patient with t(14;15)(q32;q11-13) and the corresponding germ-line region from chromosome 15. The genomic locus on chromosome 15 is clonally rearranged in about 4% of DLCL in agreement with the frequency of 15q11-13 translocations. A probe derived from the BCL8 locus on chromosome 15 detected a transcript in human testis and prostate, whereas no expression was found in spleen, thymus, and blood leukocytes. Analysis of the BCL8 cDNA clones isolated from human testis cDNA library showed that the BCL8 gene generates a major transcript of 2.6 kb and a less prominent 4.5-kb species due to differential polyadenylylation. By reverse transcription-PCR analysis of RNA extracted from frozen DLCL samples and lymphoma cell lines, BCL8 expression was detected in all patients carrying 15q11-13 abnormalities and in a fraction of randomly selected DLCL patients. These results suggest that the BCL8 gene is not normally expressed in lymphoid tissues, but its expression can be activated by chromosomal translocation or by other mechanisms in DLCL. Ectopic expression of BCL8 in a significant proportion of DLCL suggests an important role for this gene in the molecular pathogenesis of B cell lymphoma.
影响染色体区域15q11 - 13及其他各种伙伴的易位在弥漫性大细胞淋巴瘤(DLCL)中很常见。为了鉴定参与这些易位的假定基因(此处命名为BCL8),我们从一名患有t(14;15)(q32;q11 - 13)的DLCL患者中克隆了断点区域,并从15号染色体克隆了相应的种系区域。15号染色体上的基因组位点在约4%的DLCL中发生克隆性重排,这与15q11 - 13易位的频率一致。来自15号染色体上BCL8位点的探针在人类睾丸和前列腺中检测到一种转录本,而在脾脏、胸腺和血液白细胞中未发现表达。对从人类睾丸cDNA文库中分离的BCL8 cDNA克隆的分析表明,由于多聚腺苷酸化的差异,BCL8基因产生了一个2.6 kb的主要转录本和一个不太明显的4.5 kb的转录本。通过对从冷冻的DLCL样本和淋巴瘤细胞系中提取的RNA进行逆转录 - PCR分析,在所有携带15q11 - 13异常的患者以及一部分随机选择的DLCL患者中检测到了BCL8表达。这些结果表明,BCL8基因在淋巴组织中通常不表达,但其表达可通过染色体易位或DLCL中的其他机制被激活。BCL8在相当一部分DLCL中的异位表达表明该基因在B细胞淋巴瘤的分子发病机制中起重要作用。