Liyanage M, Weaver Z, Barlow C, Coleman A, Pankratz D G, Anderson S, Wynshaw-Boris A, Ried T
Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Blood. 2000 Sep 1;96(5):1940-6.
Atm-deficient mice (Atm(-/-)) recapitulate many aspects of the ataxia telangiectasia (AT) syndrome, including the susceptibility to tumors of lymphoid origin. To investigate the mechanism of tumorigenesis, we have examined a panel of 8 thymic lymphomas from Atm(-/-) mice. All Atm(-/-) tumors are of thymic lymphoblastoid origin, display an immature CD3(-) and CD4(+)/CD8(+) phenotype, and arise coincident with V(D)J recombination. Cytogenetically, all tumors are diploid or near diploid but exhibit multiple chromosome aberrations with an average of 4 abnormal chromosomes per tumor. All the tumors revealed chromosome 14 rearrangements precisely at the T-cell receptoralpha/delta (Tcralpha/delta) locus, suggesting the involvement of V(D)J recombination in these translocations. In addition, 11.5% of Atm(-/-) peripheral T cells showed chromosome 14 translocations, suggesting that rearrangements at the Tcralpha/delta locus occur early during tumor development in the absence of ATM. However, additional genetic aberrations are required for tumorigenesis. For example, translocations involving chromosome 12, often with chromosome 14 (more than 60%), and partial or complete trisomy of chromosome 15, with copy number increases of the c-myc oncogene were frequently observed. These observations suggest that ATM is required for normal rearrangement of the Tcralpha/delta locus but not for V(D)J recombination at other loci. The mechanisms that lead to tumorigenesis may be due to the involvement of ATM in monitoring double-stranded DNA breaks. (Blood. 2000;96:1940-1946)
缺乏共济失调毛细血管扩张症突变基因(Atm)的小鼠(Atm(-/-))重现了共济失调毛细血管扩张症(AT)综合征的许多方面,包括对淋巴源性肿瘤的易感性。为了研究肿瘤发生的机制,我们检测了一组来自Atm(-/-)小鼠的8个胸腺淋巴瘤。所有Atm(-/-)肿瘤均起源于胸腺淋巴母细胞,表现出不成熟的CD3(-)和CD4(+)/CD8(+)表型,并且与V(D)J重排同时出现。细胞遗传学分析显示,所有肿瘤均为二倍体或接近二倍体,但表现出多个染色体畸变,每个肿瘤平均有4条异常染色体。所有肿瘤在T细胞受体α/δ(Tcralpha/delta)基因座处均精确显示出14号染色体重排,提示V(D)J重排在这些易位中起作用。此外,11.5%的Atm(-/-)外周T细胞显示出14号染色体易位,提示在缺乏ATM的情况下,Tcralpha/delta基因座处的重排在肿瘤发生早期就已出现。然而,肿瘤发生还需要其他遗传畸变。例如,经常观察到涉及12号染色体的易位,通常与14号染色体一起(超过60%),以及15号染色体的部分或完全三体性,同时c-myc癌基因的拷贝数增加。这些观察结果表明,ATM是Tcralpha/delta基因座正常重排所必需的,但不是其他基因座V(D)J重排所必需的。导致肿瘤发生的机制可能是由于ATM参与监测双链DNA断裂。(《血液》。2000年;96:1940 - 1946)