Larson R C, Lavenir I, Larson T A, Baer R, Warren A J, Wadman I, Nottage K, Rabbitts T H
MRC Laboratory of Molecular Biology, Cambridge, UK.
EMBO J. 1996 Mar 1;15(5):1021-7.
The LMO2 and TAL1 genes were first identified via chromosomal translocations and later found to encode proteins that interact during normal erythroid development. Some T cell leukaemia patients have chromosomal abnormalities involving both genes, implying that LMO2 and TAL1 act synergistically to promote tumorigenesis after their inappropriate co-expression. To test this hypothesis, transgenic mice were made which co-express Lmo2 and Tal1 genes in T cells. Dimers of Lmo2 and Tal1 proteins were formed in thymocytes of double but not single transgenic mice. Furthermore, thymuses of double transgenic mice were almost completely populated by immature T cells from birth, and these mice develop T cell tumours approximately 3 months earlier than those with only the Lmo2 transgene. Thus interaction between these two proteins can alter T cell development and potentiate tumorigenesis. The data also provide formal proof that TAL1 is an oncogene, apparently acting as a tumour promoter in this system.
LMO2和TAL1基因最初是通过染色体易位被鉴定出来的,后来发现它们编码的蛋白质在正常红细胞发育过程中相互作用。一些T细胞白血病患者存在涉及这两个基因的染色体异常,这意味着LMO2和TAL1在不适当的共表达后协同作用促进肿瘤发生。为了验证这一假设,制作了在T细胞中共表达Lmo2和Tal1基因的转基因小鼠。Lmo2和Tal1蛋白的二聚体在双转基因小鼠而非单转基因小鼠的胸腺细胞中形成。此外,双转基因小鼠的胸腺从出生起几乎完全被未成熟T细胞占据,并且这些小鼠比仅携带Lmo2转基因的小鼠早约3个月发生T细胞肿瘤。因此,这两种蛋白质之间的相互作用可以改变T细胞发育并增强肿瘤发生。这些数据还提供了正式证据,证明TAL1是一种癌基因,在该系统中显然作为肿瘤促进因子起作用。