Panigrahi G B, Walker I G
Biochem Biophys Res Commun. 1986 Nov 14;140(3):775-81. doi: 10.1016/0006-291x(86)90701-1.
A substrate of DNA containing 4HAQO adducts, suitable for studies of excision repair, was prepared by reacting calf thymus DNA with [3H]monoacetyl-4HAQO. A crude HeLa cell extract was prepared by the method of Mortelmans et al (Proc. Natl. Acad. Sci. U.S.A. 73, 2757, 1976). The cell extract would specifically excise pyrimidine dimers from UV-irradiated DNA but would not release 4HAQO adducts in an acid soluble form. This result points to different initial steps in the excision repair process for these two forms of damage even though much of the repair mechanism is common to both.
通过使小牛胸腺DNA与[3H]单乙酰-4HAQO反应,制备了一种含有4HAQO加合物的DNA底物,适用于切除修复研究。按照莫特尔曼斯等人的方法(《美国国家科学院院刊》73卷,2757页,1976年)制备了粗制的HeLa细胞提取物。该细胞提取物能特异性地从紫外线照射的DNA中切除嘧啶二聚体,但不会以酸溶性形式释放4HAQO加合物。这一结果表明,尽管这两种形式的损伤在很大程度上具有共同的修复机制,但在切除修复过程的初始步骤有所不同。