Wong R S, Kapp L N, Dewey W C
Radiation Oncology Research Laboratory, University of California, San Francisco 94143.
Biochim Biophys Acta. 1989 Mar 1;1007(2):224-7. doi: 10.1016/0167-4781(89)90043-2.
DNA fork displacement rates (FDR) were measured in Chinese hamster ovary (CHO) cells heated at either 43.5 degrees C or 45.5 degrees C for various times. The inhibition of fork movement rate by heat was both time and temperature dependent, i.e., 10-20 min at 43.5 degrees C or 5 min at 45.5 degrees C was required to decrease the FDR to 20-30% of the control rate of 1 micron/min. Following heating, the reduced FDR was found to be constant for at least 75 min. The observed effects of heat on reduced rates of DNA replicon initiation and chain elongation and the increase in DNA with single-stranded regions could be explained by the heat sensitivity of the FDR. Any of these alterations in the DNA replication process may lead to many opportunities for abnormal DNA and/or protein interactions to occur which ultimately may lead to the observed formation of chromosomal aberrations.
在中国仓鼠卵巢(CHO)细胞中,测量了在43.5摄氏度或45.5摄氏度下加热不同时间后的DNA叉移位率(FDR)。热对叉移动速率的抑制作用既与时间有关,也与温度有关,即43.5摄氏度下10 - 20分钟或45.5摄氏度下5分钟可使FDR降至1微米/分钟的对照速率的20 - 30%。加热后,发现降低的FDR至少在75分钟内保持恒定。观察到的热对DNA复制子起始和链延伸速率降低的影响以及单链区域DNA的增加,可以通过FDR的热敏感性来解释。DNA复制过程中的任何这些改变都可能导致许多异常DNA和/或蛋白质相互作用发生的机会,最终可能导致观察到的染色体畸变的形成。