Barry J, Alberts B
Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0448.
J Biol Chem. 1994 Dec 30;269(52):33049-62.
The T4 bacteriophage gene 59 protein is required for normal T4 DNA replication. We have purified this protein to homogeneity in two steps and show that it binds both to single-stranded DNA and to the T4 gene 32 protein, a DNA single strand binding protein. In in vitro assays, covering DNA with 32 protein makes this DNA inaccessible to the 41 protein, the highly processive DNA helicase, that associates with the T4 DNA primase (gene 61 protein) to form an active primosome. However, the 59 protein brings about the rapid assembly of 41 protein onto single-stranded DNA, even if this DNA is covered with 32 protein. The 59 protein is therefore a DNA helicase assembly protein. The observed requirements for the 59 protein in the vivo T4 DNA replication are explained by there being two alternative pathways for loading the 41 protein onto a replication fork at early times of T4 DNA synthesis, with only a 59 protein-mediated pathway remaining operative for the recombination-mediated replication that dominates later in infection (Barry, J., and Alberts, B. M. (1994) J. Biol. Chem. 269, 33063-33068).
T4噬菌体基因59蛋白是正常T4 DNA复制所必需的。我们通过两步法将该蛋白纯化至同质,并表明它既能与单链DNA结合,也能与T4基因32蛋白(一种DNA单链结合蛋白)结合。在体外实验中,用32蛋白覆盖DNA会使这种DNA无法被41蛋白(高度持续合成的DNA解旋酶)接近,41蛋白与T4 DNA引发酶(基因61蛋白)结合形成活性引发体。然而,59蛋白能使41蛋白迅速组装到单链DNA上,即使该DNA被32蛋白覆盖。因此,59蛋白是一种DNA解旋酶组装蛋白。体内T4 DNA复制中对59蛋白的观察到的需求可以通过以下方式解释:在T4 DNA合成早期,将41蛋白加载到复制叉上有两条替代途径,而在感染后期占主导的重组介导的复制中,只有59蛋白介导的途径仍然有效(巴里,J.,和阿尔伯茨,B.M.(1994年)《生物化学杂志》269,33063 - 33068)。