Mivechi N F, Dewey W C
Radiat Res. 1985 Sep;103(3):337-50.
The levels of DNA polymerase alpha and beta activities were measured during the cell cycle using a total cell homogenate technique. The results indicate a decrease in the levels of both enzyme activities during the G1 phase and a gradual increase as cells enter the S phase. The recovery of DNA polymerase activities was measured after heating for 10 min at 45.5 degrees C during the G1 phase (1.5 hr after mitotic release) or S phase (8-9 hr after mitotic release). This treatment reduced the levels of DNA polymerase beta activity to 20-30% and DNA polymerase alpha activity to 40-50% of their control activity for both G1 and S phase. The activity of DNA polymerase beta recovered fully during 20-25 hr after heating for both G1 phase or S phase cells. There was no recovery of the activity of DNA polymerase alpha during this time. Survival was measured when cells were irradiated (4 Gy) at various times after hyperthermia (10 min at 45.5 degrees C), and for both G1 and S phase the interaction between heat and X rays disappeared by 20-25 hr after heating and the same increase was observed for the recovery of DNA polymerase beta activity. Furthermore, treatment with cycloheximide inhibited protein synthesis and prevented recovery from heat damage assayed in terms of both cell survival and beta polymerase activity. These results, in addition to experiments with heat protection by glycerol or thermotolerance induced with sodium arsenite or fractionated heat doses, suggest that beta polymerase may be an important enzyme involved in repairing X-ray-induced damage that can result in cell lethality.
采用全细胞匀浆技术在细胞周期中测量DNA聚合酶α和β的活性水平。结果表明,在G1期两种酶活性水平均下降,随着细胞进入S期则逐渐升高。在G1期(有丝分裂释放后1.5小时)或S期(有丝分裂释放后8 - 9小时)于45.5℃加热10分钟后,测量DNA聚合酶活性的恢复情况。这种处理使G1期和S期的DNA聚合酶β活性水平降至对照活性的20 - 30%,DNA聚合酶α活性降至对照活性的40 - 50%。对于G1期或S期细胞,加热后20 - 25小时内DNA聚合酶β的活性完全恢复。在此期间DNA聚合酶α的活性未恢复。在热疗(45.5℃10分钟)后的不同时间对细胞进行照射(4 Gy)并测量存活率,对于G1期和S期,加热后20 - 25小时热与X射线之间的相互作用消失,并且观察到DNA聚合酶β活性的恢复有相同程度的增加。此外,用环己酰亚胺处理可抑制蛋白质合成,并阻止从热损伤中恢复,这在细胞存活率和β聚合酶活性方面均有检测。这些结果,除了用甘油进行热保护或用亚砷酸钠或分次热剂量诱导耐热性的实验外,表明β聚合酶可能是参与修复可导致细胞致死的X射线诱导损伤的一种重要酶。