Ishizaka Y, Chernov M V, Burns C M, Stark G R
Department of Molecular Biology, Cleveland Clinic Foundation, OH 44195, USA.
Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3224-8. doi: 10.1073/pnas.92.8.3224.
The rat cell line REF52 is not permissive for gene amplification. Simian virus 40 tumor (T) antigen converts these cells to a permissive state, as do dominant negative mutants of p53, suggesting that the effect of T antigen is due mainly to its ability to bind to p53. To manipulate permissivity, we introduced a temperature-sensitive mutant of T antigen (tsA58) into REF52 cells and selected for resistance to N-(phosphonacetyl)-L-aspartate (PALA). Most freshly isolated PALA-resistant colonies, each of approximately 200 cells, selected at a permissive temperature, arrested when shifted to a nonpermissive temperature. Growth arrest was stable, with no evidence of apoptosis, as long as T antigen was absent but was reversed when T antigen was restored. In contrast, PALA-resistant clones grown to approximately 10(7) cells at a permissive temperature did not arrest when shifted to a nonpermissive temperature. All PALA-resistant clones examined had amplified carbamoyl-phosphate synthetase-aspartate transcarbamoylase-dihydroorotase (CAD) genes, present in structures consistent with a mechanism involving bridge-breakage-fusion (BBF) cycles. We propose that p53-mediated growth arrest operates only early during the complex process of gene amplification, when newly formed PALA-resistant cells contain broken DNA, generated in BBF cycles. During propagation under permissive conditions, the broken DNA ends are healed, and, even though the p53-mediated pathway is still intact at a nonpermissive temperature and the cells contain amplified DNA, they are not arrested in the absence of broken DNA. The data support the hypothesis that BBF cycles are an important mechanism of amplification and that the broken DNA generated in each cycle is a key signal that regulates permissivity for gene amplification.
大鼠细胞系REF52不允许基因扩增。猿猴病毒40肿瘤(T)抗原可将这些细胞转变为允许状态,p53的显性负突变体也有此作用,这表明T抗原的作用主要归因于其与p53结合的能力。为了操控允许性,我们将T抗原的温度敏感突变体(tsA58)导入REF52细胞,并筛选对N-(膦酰乙酰基)-L-天冬氨酸(PALA)具有抗性的细胞。在允许温度下筛选出的大多数新鲜分离的对PALA具有抗性的菌落,每个菌落约200个细胞,转移到非允许温度时会停滞生长。只要没有T抗原,生长停滞就是稳定的,没有凋亡迹象,但当恢复T抗原时,生长停滞会被逆转。相比之下,在允许温度下生长到约10^7个细胞的对PALA具有抗性的克隆,转移到非允许温度时不会停滞生长。所有检测的对PALA具有抗性的克隆都扩增了氨甲酰磷酸合成酶-天冬氨酸转氨甲酰酶-二氢乳清酸酶(CAD)基因,其存在的结构与涉及桥断裂-融合(BBF)循环的机制一致。我们提出,p53介导的生长停滞仅在基因扩增的复杂过程早期起作用,此时新形成的对PALA具有抗性的细胞含有在BBF循环中产生的断裂DNA。在允许条件下繁殖期间,断裂的DNA末端会愈合,并且,即使在非允许温度下p53介导的途径仍然完整且细胞含有扩增的DNA,但在没有断裂DNA的情况下它们不会停滞生长。这些数据支持以下假说:BBF循环是扩增的重要机制,并且每个循环中产生的断裂DNA是调节基因扩增允许性的关键信号。