Ortiz T, Edreira A, Piñero J
Department of Cell Biology, Faculty of Biology, University of Seville, Avd. Reina Mercedes s/n, 41012 Seville, Spain.
Radiat Environ Biophys. 2002 Jun;41(2):149-53. doi: 10.1007/s00411-001-0129-0.
We have tested the ability of T4 DNA ligase to rejoin radiation-induced DNA strand breaks in living hamster cells (CHO-K1, EM9, xrs-5). T4 DNA ligase was introduced into cells by electroporation prior to x-irradiation. Single- and double-strand breaks were measured by the alkaline comet assay technique, and double-strand breaks (DSBs) were evaluated by the pulsed-field gel electrophoresis method. In the comet assay, the three cell lines showed reduced tail moments following pretreatment with T4 DNA ligase, both directly after irradiation and after repair incubation for 4 h. Similarly, the results obtained from pulsed-field gel electrophoresis showed reduced DSB frequencies after pretreatment with T4 DNA ligase. We conclude that exogeneous T4 ligase contributes to rejoining of radiation-induced strand breaks.
我们测试了T4 DNA连接酶修复活体仓鼠细胞(CHO-K1、EM9、xrs-5)中辐射诱导的DNA链断裂的能力。在X射线照射之前,通过电穿孔将T4 DNA连接酶导入细胞。采用碱性彗星试验技术测量单链和双链断裂,并通过脉冲场凝胶电泳法评估双链断裂(DSB)。在彗星试验中,这三种细胞系在照射后立即以及修复培养4小时后,经T4 DNA连接酶预处理后尾部矩均降低。同样,脉冲场凝胶电泳的结果表明,经T4 DNA连接酶预处理后DSB频率降低。我们得出结论,外源性T4连接酶有助于辐射诱导的链断裂的重新连接。