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DNA中辐射诱导链断裂的体外修复

In vitro repair of radiation-induced strand breaks in DNA.

作者信息

Mitzel-Landbeck L, Schutz G, Hagen U

出版信息

Biochim Biophys Acta. 1976 May 3;432(2):145-53. doi: 10.1016/0005-2787(76)90156-8.

Abstract

DNA, gamma-irradiated in vitro or in isolated thymocytes was treated with several enzymes to achieve repair of the radiation-induced single strand braks. Whereas an incubation with polynucleotide ligase can join only 25% of the single strand breaks, a combined treatemnt with exonuclease III (EC 3.1.4.1), DNA polymerase I (EC 2.7.7.7), and polynucleotide ligase leads to repair of 80% of the breaks. For this in vitro repair the exonuclease III has to remove several, probably damaged, nucleotides from the 3'-terminal producing a single-stranded gap, which will be filled in by DNA polymerase I and joined by ligase. Tests for successful rejoining of the strand breaks were performed by showing the loss of primer 3'-OH sites for DNA polymerase I, by the resistance of incorporated nucleotides in the gap to removal by a second exonuclease III treatment, and by strand break determination in the analytical ultracentrifuge. 20% of the radiation-induced strand breaks will not be repaired by this combined treatment possibly due to an incomplete binding of the ligase on the 5'-terminals and/or an incomplete removal of the damaged 3'-terminals by exonuclease III.

摘要

体外或在分离的胸腺细胞中经γ射线照射的DNA,用几种酶处理以修复辐射诱导的单链断裂。虽然用多核苷酸连接酶温育只能连接25%的单链断裂,但用核酸外切酶III(EC 3.1.4.1)、DNA聚合酶I(EC 2.7.7.7)和多核苷酸连接酶联合处理可使80%的断裂得到修复。对于这种体外修复,核酸外切酶III必须从3'-末端去除几个可能受损的核苷酸,产生一个单链缺口,该缺口将由DNA聚合酶I填充并由连接酶连接。通过显示DNA聚合酶I的引物3'-OH位点的丧失、通过缺口处掺入的核苷酸对第二次核酸外切酶III处理去除的抗性以及通过分析超速离心中的链断裂测定,对链断裂的成功重新连接进行了测试。20%的辐射诱导的链断裂不能通过这种联合处理修复,这可能是由于连接酶在5'-末端的结合不完全和/或核酸外切酶III对受损3'-末端的去除不完全。

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