Sono A, Sakaguchi K
Mutat Res. 1981 Jan;80(1):121-31. doi: 10.1016/0027-5107(81)90182-2.
Cycloheximide (CH) and puromycin (PM)strongly antagonize induction of sister-chromatid exchanges (SCEs) by exogenous agents regardless of the mechanism for initiating damage. 5-Bromodeoxyuridine (BUdR) substitution was used to monitor SCEs, but the background level of BUdR-induced SCEs was unaffected by the presence of protein inhibitors. Antagonism between DNA-damaging agents and protein inhibitors was strongest in euchromatic regions. Possible relationships between SCE formation and the mechanism of antagonism by protein inhibitors are discussed.
放线菌酮(CH)和嘌呤霉素(PM)能强烈拮抗外源性试剂诱导的姐妹染色单体交换(SCEs),无论引发损伤的机制如何。采用5-溴脱氧尿苷(BUdR)替代法监测SCEs,但蛋白质抑制剂的存在并不影响BUdR诱导的SCEs的背景水平。在常染色质区域,DNA损伤剂与蛋白质抑制剂之间的拮抗作用最强。本文讨论了SCE形成与蛋白质抑制剂拮抗机制之间可能的关系。