Bennett C B, Westmoreland T J, Snipe J R, Resnick M A
Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Mol Cell Biol. 1996 Aug;16(8):4414-25. doi: 10.1128/MCB.16.8.4414.
Human chromosomal DNA contains many repeats which might provide opportunities for DNA repair. We have examined the consequences of a single double-strand break (DSB) within a 360-kb dispensable yeast artificial chromosome (YAC) containing human DNA (YAC12). An Alu-URA3-YZ sequence was targeted to several Alu sites within the YAC in strains of the yeast Saccharomyces cerevisiae; the strains contained a galactose-inducible HO endonuclease that cut the YAC at the YZ site. The presence of a DSB in most YACs led to deletion of the URA3 cassette, with retention of the telomeric markers, through recombination between surrounding Alus. For two YACs, the DSBs were not repaired and there was a G2 delay associated with the persistent DSBs. The presence of persistent DSBs resulted in cell death even though the YACs were dispensable. Among the survivors of the persistent DSBs, most had lost the YAC. By a pullback procedure, cell death was observed to begin at least 6 h after induction of a break. For YACs in which the DSB was rapidly repaired, the breaks did not cause cell cycle delay or lead to cell death. These results are consistent with our previous conclusion that a persistent DSB in a plasmid (YZ-CEN) also caused lethality (C. B. Bennett, A. L. Lewis, K. K. Baldwin, and M. A. Resnick, Proc. Natl. Acad. Sci. USA 90:5613-5617, 1993). However, a break in the YZ-CEN plasmid did not induce lethality in the strain (CBY) background used in the present study. The differences in survival levels appear to be due to the rapid degradation of the plasmid in the CBY strain. We, therefore, propose that for a DSB to cause cell cycle delay and death by means other than the loss of essential genetic material, it must remain unrepaired and be long-lived.
人类染色体DNA包含许多重复序列,这可能为DNA修复提供机会。我们研究了在一个含有人类DNA的360 kb可丢弃酵母人工染色体(YAC)(YAC12)内单个双链断裂(DSB)的后果。在酿酒酵母菌株中,一个Alu - URA3 - YZ序列被靶向到YAC内的几个Alu位点;这些菌株含有半乳糖诱导型HO内切酶,该酶在YZ位点切割YAC。大多数YAC中DSB的存在导致URA3盒缺失,通过周围Alu之间的重组保留了端粒标记。对于两个YAC,DSB未被修复,并且存在与持续DSB相关的G2期延迟。即使YAC是可丢弃的,持续DSB的存在仍导致细胞死亡。在持续DSB的幸存者中,大多数失去了YAC。通过回拉程序,观察到细胞死亡至少在诱导断裂后6小时开始。对于DSB迅速修复的YAC,这些断裂不会导致细胞周期延迟或细胞死亡。这些结果与我们之前的结论一致,即质粒(YZ - CEN)中的持续DSB也会导致致死性(C. B. 贝内特、A. L. 刘易斯、K. K. 鲍德温和M. A. 雷斯尼克,《美国国家科学院院刊》90:5613 - 5617,1993)。然而,在本研究使用的菌株(CBY)背景下,YZ - CEN质粒中的断裂并未诱导致死性。存活水平的差异似乎是由于CBY菌株中质粒的快速降解。因此,我们提出,要使DSB通过除必需遗传物质丢失以外的方式导致细胞周期延迟和死亡,它必须保持未修复且寿命长。