Thompson B J, Camien M N, Warner R C
Proc Natl Acad Sci U S A. 1976 Jul;73(7):2299-303. doi: 10.1073/pnas.73.7.2299.
The rate of branch migration in double stranded DNA has been measured by the use of a unique substrate formed by the action of the EcoRI restriction endonuclease on the dimeric figure-8 configuration of the replicative form DNA of phage G4. The figure-8 and the X-form derived from it contain a junction of the kind postulated to occur in the Holliday structure and to be an essential feature of a number of models of recombination. In the X-form this junction can branch migrate to an irreversible terminal configuration consisting of two linear monomers. The disappearance of X-forms was measured by electron microscopy. A treatment of branch migration as a random walk process was developed to permit the determination of the rate of the intrinsic process, a step movement of the junction by a distance of one base pair. A value of about 6 kilobase pairs per sec at 37 degrees was obtained.
通过使用由EcoRI限制性内切核酸酶作用于噬菌体G4复制型DNA的二聚体8字形结构而形成的独特底物,已测量了双链DNA中的分支迁移速率。8字形及其衍生的X形包含一种假定发生在霍利迪结构中的连接,并且是许多重组模型的一个基本特征。在X形中,这种连接可以分支迁移到由两个线性单体组成的不可逆末端构型。通过电子显微镜测量X形的消失。开发了一种将分支迁移视为随机游走过程的方法,以确定内在过程的速率,即连接点以一个碱基对的距离进行的一步移动。在37摄氏度时获得的值约为每秒6千碱基对。