Teng S C, Chang J, McCowan B, Zakian V A
Department of Molecular Biology, Princeton University, New Jersey 08544, USA.
Mol Cell. 2000 Oct;6(4):947-52. doi: 10.1016/s1097-2765(05)00094-8.
Type II survivors arise in Saccharomyces cells lacking telomerase by a recombinational pathway that results in very long and heterogeneous length telomeres. Here we show that type II telomeres appeared abruptly in a population of cells with very short telomeres. Once established, these long telomeres progressively shortened. Short telomeres were substrates for rare, one-step lengthening events. The generation of type II survivors was absolutely Rad50p dependent. In a telomerase-proficient cell, the telomere-binding Rif proteins inhibited telomerase lengthening of telomeres. In a telomerase-deficient strain, Rif proteins, especially Rif2p, inhibited type II recombination. These data argue that only short telomeres are substrates for type II recombination and suggest that the donor for this recombination is not a chromosomal telomere.
II型幸存者出现在缺乏端粒酶的酿酒酵母细胞中,通过一种重组途径产生非常长且长度异质的端粒。在这里,我们表明II型端粒在具有非常短端粒的细胞群体中突然出现。一旦形成,这些长端粒会逐渐缩短。短端粒是罕见的一步延长事件的底物。II型幸存者的产生绝对依赖于Rad50p。在端粒酶功能正常的细胞中,端粒结合蛋白Rif抑制端粒酶对端粒的延长。在端粒酶缺陷型菌株中,Rif蛋白,尤其是Rif2p,抑制II型重组。这些数据表明只有短端粒是II型重组的底物,并表明这种重组的供体不是染色体端粒。