Bianco Piero
Department of Microbiology and Immunology, Center for Single Molecule Biophysics, University at Buffalo, Buffalo, NY 14214, USA.
Methods. 2016 Oct 1;108:40-7. doi: 10.1016/j.ymeth.2016.06.002. Epub 2016 Jun 6.
During DNA replication, forks often stall and require restart. One mechanism for restart requires that the fork be moved in a direction opposite to that of replication. This reaction is known as fork regression. For this reaction to occur, the enzyme must couple unwinding of the nascent heteroduplex fork arms to the rewinding of nascent strands ahead of itself and to the parental duplex in its wake. As the arms of the fork are complementary, this reaction is isoenergetic making it challenging to study. To overcome this, a novel adaptation of magnetic tweezers was developed by the Croquette group. Here, a 1200bp hairpin was attached at opposite ends to a flow cell surface and a magnetic bead. By manipulating the bead with the magnets, force can be applied to unwind the hairpin or alternatively, released to allow the hairpin to rewind. This adaptation was used to study fork regression by RecG. The results show that this is an efficient regression enzyme, able to work against a large opposing force. Critically, it couples DNA unwinding to duplex rewinding and in the process, can displace bound proteins from fork arms.
在DNA复制过程中,复制叉常常会停滞并需要重新启动。一种重新启动的机制要求复制叉朝着与复制相反的方向移动。这种反应被称为复制叉回归。为了使这种反应发生,该酶必须将新生异源双链复制叉臂的解旋与自身前方新生链的重新缠绕以及其后方亲本双链的重新缠绕相耦合。由于复制叉的臂是互补的,这种反应是等能的,这使得研究具有挑战性。为了克服这一点,克罗凯特团队开发了一种新型的磁镊技术。在这里,一个1200bp的发夹在相对两端分别连接到流动池表面和一个磁珠上。通过用磁铁操纵磁珠,可以施加力来解开发夹,或者相反,释放力以使发夹重新缠绕。这种改进被用于研究RecG介导的复制叉回归。结果表明,这是一种高效的回归酶,能够抵抗较大的反向力。至关重要的是,它将DNA解旋与双链重新缠绕相耦合,并且在此过程中,可以从复制叉臂上置换结合的蛋白质。