Ganesan A K, Seawell P C, Lewis R J, Hanawalt P C
Biochemistry. 1986 Sep 23;25(19):5751-5. doi: 10.1021/bi00367a060.
We previously reported that endonuclease V of bacteriophage T4 reacts processively with pyrimidine dimers in UV-irradiated DNA, tending to react with all of the dimers on one DNA molecule before reacting with any dimers on another DNA molecule [Lloyd, R. S., Hanawalt, P. C., & Dodson, M. L. (1980) Nucleic Acids Res. 8, 5113-5127]. In this paper we show that this processivity depends upon salt concentration: it can be detected in 10 mM NaCl but not, by our methods, in 100 mM NaCl. In addition, we show that endonuclease V binds to unirradiated DNA in 10 mM NaCl but not in 100 mM NaCl. We conclude that T4 endonuclease V binds to pyrimidine dimers in a two-step process in 10 mM NaCl. It first binds electrostatically to undamaged sections of DNA, and it remains bound during the second step in which it "searches" for pyrimidine dimers. Our conclusion is analogous to the expanded target theory developed for Lac repressor [Berg, O. G., Winter, R. B., & von Hippel, P. H. (1981) Biochemistry 20, 6929-6948].
我们之前报道过,噬菌体T4的核酸内切酶V能与紫外线照射过的DNA中的嘧啶二聚体进行持续性反应,倾向于在与另一个DNA分子上的任何二聚体反应之前,先与一个DNA分子上的所有二聚体反应[劳埃德,R.S.,哈纳瓦尔特,P.C.,&多德森,M.L.(1980年)《核酸研究》8,5113 - 5127]。在本文中我们表明,这种持续性取决于盐浓度:在10 mM氯化钠中可以检测到,但按照我们的方法,在100 mM氯化钠中检测不到。此外,我们表明核酸内切酶V在10 mM氯化钠中能与未照射的DNA结合,但在100 mM氯化钠中不能。我们得出结论,在10 mM氯化钠中,T4核酸内切酶V以两步过程与嘧啶二聚体结合。它首先通过静电作用与DNA的未损伤部分结合,并且在第二步“搜索”嘧啶二聚体的过程中一直保持结合状态。我们的结论类似于为乳糖阻遏物所提出的扩展靶标理论[伯格,O.G.,温特,R.B.,&冯·希佩尔,P.H.(1981年)《生物化学》20,6929 - 6948]。