Giannoni P, Fronza G, Scarabelli L, Fugassa E, Orunesu M, Cesarone C F
Institute of General Physiology, University of Genoa, Italy.
Boll Soc Ital Biol Sper. 1991 May;67(5):509-16.
Previous studies have demonstrated that DNA topoisomerase I activity can be closely related to DNA replication and active transcription in different experimental models. This relationship was further investigated by studying the time course of DNA topoisomerase I activity in cultured rat hepatocytes stimulated by epidermal growth factor. This mitogen has been shown to stimulate DNA synthesis in liver cells both in vivo and in vitro. DNA topoisomerase I activity was assayed quantifying ATP-independent relaxation of a negatively supercoiled plasmid, substrate for the enzyme. Incubation of cellular extracts was carried out at 30 degrees C for 15'. Products were electrophoresed and analyzed by densitometry. DNA synthesis was measured as [3H]thymidine incorporation in the hepatocytes, after a 2 hrs pulse labelling. An increase in DNA topoisomerase I activity was observed early after epidermal growth factor addition, before the onset of DNA synthesis. Concomitant administration of orotic acid, which has recently shown mitoinhibitory effect, abolished the EGF-induced activity as well as DNA synthesis. Taken together these data indicate that, in cultured hepatocytes, the induction of DNA synthesis is supported by DNA topoisomerase I with a precise time schedule. Orotic acid administration abolishes this response and causes an overall loss in DNA topoisomerase I activity.
先前的研究表明,在不同的实验模型中,DNA拓扑异构酶I的活性可能与DNA复制和活跃转录密切相关。通过研究表皮生长因子刺激的培养大鼠肝细胞中DNA拓扑异构酶I活性的时间进程,对这种关系进行了进一步研究。这种有丝分裂原已被证明在体内和体外均可刺激肝细胞中的DNA合成。通过定量测定该酶的底物——负超螺旋质粒的ATP非依赖性松弛来检测DNA拓扑异构酶I的活性。细胞提取物在30℃孵育15分钟。产物进行电泳并通过密度测定法进行分析。在2小时的脉冲标记后,通过测量肝细胞中[3H]胸苷的掺入量来测定DNA合成。在添加表皮生长因子后早期,在DNA合成开始之前,观察到DNA拓扑异构酶I活性增加。同时给予最近显示出有丝分裂抑制作用的乳清酸,可消除表皮生长因子诱导的活性以及DNA合成。综合这些数据表明,在培养的肝细胞中,DNA拓扑异构酶I以精确的时间安排支持DNA合成的诱导。给予乳清酸可消除这种反应,并导致DNA拓扑异构酶I活性全面丧失。