Finger L R, Kagan J, Christopher G, Kurtzberg J, Hershfield M S, Nowell P C, Croce C M
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140.
Proc Natl Acad Sci U S A. 1989 Jul;86(13):5039-43. doi: 10.1073/pnas.86.13.5039.
We analyzed a t(1;14)(p32;q11) chromosomal translocation in a human lymphohemopoietic stem cell line derived from a patient with acute T-lymphoblastic leukemia. The chromosomal joining on the 1p+ chromosome occurred at the T-cell receptor delta diversity (D delta 2) segment, and the reciprocal chromosomal joining on the 14q- chromosome occurred at the T-cell delta diversity segment D delta 1. The involvement of delta diversity segments at the translocation junctions suggests that the translocation occurred during an attempt at D delta 1-D delta 2 joining in a stem cell. The segment of chromosome 1 at band p32, adjacent to the chromosomal breakpoint, encodes a transcriptional unit designated TCL5 (T-cell leukemia/lymphoma 5). The differential expression of the TCL5 RNA transcripts in this lymphohemopoietic stem cell line relative to several other T- and B-cell lines suggests that TCL5 gene expression is an integral event in the pathogenesis of the T-cell leukemia. Rearrangement of the TCL5 locus in a human melanoma cell line carrying a del(1p32) further implies that the TCL5 gene may play a role in malignant transformation.
我们分析了一名急性T淋巴细胞白血病患者来源的人淋巴造血干细胞系中的t(1;14)(p32;q11)染色体易位。1p+染色体上的染色体连接发生在T细胞受体δ多样性(Dδ2)区段,而14q-染色体上的相互染色体连接发生在T细胞δ多样性区段Dδ1。易位连接处δ多样性区段的参与表明,该易位发生在干细胞中Dδ1-Dδ2连接的尝试过程中。位于染色体1 p32带、与染色体断点相邻的区段编码一个名为TCL5(T细胞白血病/淋巴瘤5)的转录单位。相对于其他几种T细胞和B细胞系,该淋巴造血干细胞系中TCL5 RNA转录本的差异表达表明,TCL5基因表达是T细胞白血病发病机制中的一个不可或缺的事件。在携带del(1p32)的人黑色素瘤细胞系中TCL5基因座的重排进一步表明,TCL5基因可能在恶性转化中起作用。