Howard Hughes Medical Institute, Cornell University, Ithaca, NY, 14853, USA.
Physics Department & LASSP, Cornell University, Ithaca, NY, 14853, USA.
Nat Commun. 2018 Jun 13;9(1):2306. doi: 10.1038/s41467-018-04702-x.
To ensure accurate DNA replication, a replisome must effectively overcome numerous obstacles on its DNA substrate. After encountering an obstacle, a progressing replisome often aborts DNA synthesis but continues to unwind. However, little is known about how DNA synthesis is resumed downstream of an obstacle. Here, we examine the consequences of a non-replicating replisome collision with a co-directional RNA polymerase (RNAP). Using single-molecule and ensemble methods, we find that T7 helicase interacts strongly with a non-replicating T7 DNA polymerase (DNAP) at a replication fork. As the helicase advances, the associated DNAP also moves forward. The presence of the DNAP increases both helicase's processivity and unwinding rate. We show that such a DNAP, together with its helicase, is indeed able to actively disrupt a stalled transcription elongation complex, and then initiates replication using the RNA transcript as a primer. These observations exhibit T7 helicase's novel role in replication re-initiation.
为了确保准确的 DNA 复制,复制体必须有效地克服其 DNA 底物上的许多障碍。遇到障碍后,前进的复制体通常会中止 DNA 合成,但会继续解旋。然而,对于如何在障碍物下游恢复 DNA 合成知之甚少。在这里,我们研究了与共向 RNA 聚合酶 (RNAP) 碰撞的非复制复制体的后果。使用单分子和整体方法,我们发现 T7 解旋酶在复制叉处与非复制 T7 DNA 聚合酶 (DNAP) 强烈相互作用。随着解旋酶的前进,相关的 DNAP 也向前移动。DNAP 的存在增加了解旋酶的连续性和解旋速度。我们表明,这样的 DNAP 及其解旋酶确实能够主动破坏停滞的转录延伸复合物,然后使用 RNA 转录本作为引物启动复制。这些观察结果展示了 T7 解旋酶在复制重新起始中的新作用。