Akasaka T, Miura I, Takahashi N, Akasaka H, Yonetani N, Ohno H, Fukuhara S, Okuma M
Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
Cancer Res. 1997 Jan 1;57(1):7-12.
3q27 translocations affecting the BCL6 gene can involve not only immunoglobulin genes (IG) but also other as yet uncharacterized chromosomal loci as partners. Here, we describe cloning of the junctional area of a recurring translocation, t(3;6)(q27;p21), in non-Hodgkin's lymphoma of B-cell type and isolation of clones from 6p21; high resolution fluorescence in situ hybridization mapped the clones to sub-band 6p21.3. Nucleotide sequence analysis of a fragment from the junctional area of 6p21 revealed the presence of a novel H4 histone gene that was included in the histone gene cluster on this particular region, and the same fragment detected approximately 380-bp transcripts in hematological tumor cells. Breakpoints on 3q27 of two cases carrying t(3;6) were immediately 3' of the BCL6 exon 1, and the H4 histone gene was substituted for the 5' regulatory elements of BCL6. Because H4 gene expression is tightly coupled to DNA replication, this study suggested an immediate mechanism for deregulated expression of BCL6, leading to the development of non-Hodgkin's lymphoma.
影响BCL6基因的3q27易位不仅可累及免疫球蛋白基因(IG),还可累及其他尚未明确特征的染色体位点作为伙伴。在此,我们描述了在B细胞型非霍奇金淋巴瘤中一种复发性易位t(3;6)(q27;p21)连接区的克隆以及从6p21分离出的克隆;高分辨率荧光原位杂交将这些克隆定位到6p21.3亚带。对6p21连接区一个片段的核苷酸序列分析显示存在一个新的H4组蛋白基因,该基因包含在该特定区域的组蛋白基因簇中,并且同一片段在血液肿瘤细胞中检测到约380 bp的转录本。两例携带t(3;6)的病例在3q27上的断点紧邻BCL6外显子1的3'端,H4组蛋白基因取代了BCL6的5'调控元件。由于H4基因表达与DNA复制紧密相关,本研究提示了一种BCL6表达失调的直接机制,导致非霍奇金淋巴瘤的发生。