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T细胞淋巴瘤/白血病细胞系中6q21 - 22断点区域的分子细胞遗传学分析

Molecular cytogenetic analysis of the breakpoint region at 6q21-22 in T-cell lymphoma/leukemia cell lines.

作者信息

Tagawa Hiroyuki, Miura Ikuo, Suzuki Ritsuro, Suzuki Hiroko, Hosokawa Yoshitaka, Seto Masao

机构信息

Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

Genes Chromosomes Cancer. 2002 Jun;34(2):175-85. doi: 10.1002/gcc.10057.

Abstract

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.

摘要

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。

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