Tagawa Hiroyuki, Miura Ikuo, Suzuki Ritsuro, Suzuki Hiroko, Hosokawa Yoshitaka, Seto Masao
Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.
Genes Chromosomes Cancer. 2002 Jun;34(2):175-85. doi: 10.1002/gcc.10057.
Chromosome band 6q21 is reported to be one of the most frequent target regions in T-cell lymphoma for both translocations and deletions. To explore whether the breakpoint clustering in T-cell malignancy indicates the presence of a common breakpoint region in 6q, we employed fluorescence in situ hybridization analysis using various YAC, BAC, and PAC clones aligned at 6q21-22. We identified two T-cell lymphoma/leukemia cell lines with different differentiation stages that had breakpoints within the same novel gene, TCBA1 (T-cell lymphoma breakpoint associated target 1). In a T-cell lymphoblastic lymphoma cell line, HT-1, the TCBA1 fused to SUSP1 (SUMO-1-specific protease), creating a SUSP1-TCBA1 chimeric gene. However, in an adult T-cell leukemia cell line, ATN-1, no chimeric gene was detected, although aberrant TCBA1 transcripts were produced. We conclude that TCBA1 is a possible target gene for T-cell lineage-specific chromosome aberrations at 6q21.
据报道,染色体6q21带是T细胞淋巴瘤中易位和缺失最常见的靶区域之一。为了探究T细胞恶性肿瘤中的断点聚集是否表明6q存在一个常见的断点区域,我们使用了荧光原位杂交分析,该分析采用了排列在6q21 - 22区域的各种酵母人工染色体(YAC)、细菌人工染色体(BAC)和噬菌体人工染色体(PAC)克隆。我们鉴定出两个处于不同分化阶段的T细胞淋巴瘤/白血病细胞系,它们在同一个新基因TCBA1(T细胞淋巴瘤断点相关靶标1)内存在断点。在一个T细胞淋巴母细胞淋巴瘤细胞系HT - 1中,TCBA1与SUSP1(SUMO - 1特异性蛋白酶)融合,产生了一个SUSP1 - TCBA1嵌合基因。然而,在一个成人T细胞白血病细胞系ATN - 1中,尽管产生了异常的TCBA1转录本,但未检测到嵌合基因。我们得出结论,TCBA1是6q21处T细胞谱系特异性染色体畸变的一个可能的靶基因。