Wu Colin G, Lohman Timothy M
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, 660 South Euclid Avenue, Box 8231, St. Louis, MO 63110, USA.
J Mol Biol. 2008 Oct 3;382(2):312-26. doi: 10.1016/j.jmb.2008.07.012. Epub 2008 Jul 16.
Escherichia coli RecBCD is a bipolar DNA helicase possessing two motor subunits (RecB, a 3'-to-5' translocase, and RecD, a 5'-to-3' translocase) that is involved in the major pathway of recombinational repair. Previous studies indicated that the minimal kinetic mechanism needed to describe the ATP-dependent unwinding of blunt-ended DNA by RecBCD in vitro is a sequential n-step mechanism with two to three additional kinetic steps prior to initiating DNA unwinding. Since RecBCD can "melt out" approximately 6 bp upon binding to the end of a blunt-ended DNA duplex in a Mg(2+)-dependent but ATP-independent reaction, we investigated the effects of noncomplementary single-stranded (ss) DNA tails [3'-(dT)(6) and 5'-(dT)(6) or 5'-(dT)(10)] on the mechanism of RecBCD and RecBC unwinding of duplex DNA using rapid kinetic methods. As with blunt-ended DNA, RecBCD unwinding of DNA possessing 3'-(dT)(6) and 5'-(dT)(6) noncomplementary ssDNA tails is well described by a sequential n-step mechanism with the same unwinding rate (mk(U)=774+/-16 bp s(-1)) and kinetic step size (m=3.3+/-1.3 bp), yet two to three additional kinetic steps are still required prior to initiation of DNA unwinding (k(C)=45+/-2 s(-1)). However, when the noncomplementary 5' ssDNA tail is extended to 10 nt [5'-(dT)(10) and 3'-(dT)(6)], the DNA end structure for which RecBCD displays optimal binding affinity, the additional kinetic steps are no longer needed, although a slightly slower unwinding rate (mk(U)=538+/-24 bp s(-1)) is observed with a similar kinetic step size (m=3.9+/-0.5 bp). The RecBC DNA helicase (without the RecD subunit) does not initiate unwinding efficiently from a blunt DNA end. However, RecBC does initiate well from a DNA end possessing noncomplementary twin 5'-(dT)(6) and 3'-(dT)(6) tails, and unwinding can be described by a simple uniform n-step sequential scheme, without the need for the additional k(C) initiation steps, with a similar kinetic step size (m=4.4+/-1.7 bp) and unwinding rate (mk(obs)=396+/-15 bp s(-1)). These results suggest that the additional kinetic steps with rate constant k(C) required for RecBCD to initiate unwinding of blunt-ended and twin (dT)(6)-tailed DNA reflect processes needed to engage the RecD motor with the 5' ssDNA.
大肠杆菌RecBCD是一种双极DNA解旋酶,拥有两个运动亚基(RecB,一种3'至5'转位酶,和RecD,一种5'至3'转位酶),参与重组修复的主要途径。先前的研究表明,描述RecBCD在体外对平端DNA进行ATP依赖性解旋所需的最小动力学机制是一种连续的n步机制,在开始DNA解旋之前还有两到三个额外的动力学步骤。由于RecBCD在与平端DNA双链体末端结合时,能在依赖Mg(2+)但不依赖ATP的反应中“熔解出”约6个碱基对,我们使用快速动力学方法研究了非互补单链(ss)DNA尾巴[3'-(dT)(6)和5'-(dT)(6)或5'-(dT)(10)]对RecBCD和RecBC解开双链DNA机制的影响。与平端DNA一样,RecBCD解开具有3'-(dT)(6)和5'-(dT)(6)非互补ssDNA尾巴的DNA,可以用一种连续的n步机制很好地描述,其解旋速率相同(mk(U)=774±16碱基对/秒),动力学步长相同(m=3.3±1.3碱基对),但在开始DNA解旋之前仍需要两到三个额外的动力学步骤(k(C)=45±2秒(-1))。然而,当非互补的5' ssDNA尾巴延长到10个核苷酸[5'-(dT)(10)和3'-(dT)(6)]时,RecBCD对其显示出最佳结合亲和力的DNA末端结构,此时不再需要额外的动力学步骤,尽管观察到解旋速率略慢(mk(U)=538±24碱基对/秒),但动力学步长相似(m=3.9±0.5碱基对)。RecBC DNA解旋酶(没有RecD亚基)不能从平端DNA有效地启动解旋。然而,RecBC能从具有非互补的双5'-(dT)(6)和3'-(dT)(6)尾巴的DNA末端很好地启动解旋,解旋可以用一个简单的均匀n步连续方案来描述,不需要额外的k(C)启动步骤,动力学步长相似(m=4.4±1.7碱基对),解旋速率(mk(obs)=396±15碱基对/秒)。这些结果表明,RecBCD启动平端和双(dT)(6)尾巴DNA解旋所需的具有速率常数k(C)的额外动力学步骤,反映了使RecD马达与5' ssDNA结合所需的过程。