Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Laboratory of Molecular Electron Microscopy, The Rockefeller University, New York, NY 10065, USA.
Mol Cell. 2021 Jan 21;81(2):281-292.e8. doi: 10.1016/j.molcel.2020.11.013. Epub 2020 Dec 8.
Rho is a general transcription termination factor playing essential roles in RNA polymerase (RNAP) recycling, gene regulation, and genomic stability in most bacteria. Traditional models of transcription termination postulate that hexameric Rho loads onto RNA prior to contacting RNAP and then translocates along the transcript in pursuit of the moving RNAP to pull RNA from it. Here, we report the cryoelectron microscopy (cryo-EM) structures of two termination process intermediates. Prior to interacting with RNA, Rho forms a specific "pre-termination complex" (PTC) with RNAP and elongation factors NusA and NusG, which stabilize the PTC. RNA exiting RNAP interacts with NusA before entering the central channel of Rho from the distal C-terminal side of the ring. We map the principal interactions in the PTC and demonstrate their critical role in termination. Our results support a mechanism in which the formation of a persistent PTC is a prerequisite for termination.
Rho 是一种普遍转录终止因子,在大多数细菌的 RNA 聚合酶 (RNAP) 回收、基因调控和基因组稳定性中发挥着重要作用。传统的转录终止模型假定六聚体 Rho 在与 RNAP 接触之前加载到 RNA 上,然后沿着转录本移动,追赶移动的 RNAP,从而从 RNA 中拉出来。在这里,我们报告了两个终止过程中间产物的冷冻电镜 (cryo-EM) 结构。在与 RNA 相互作用之前,Rho 与 RNAP 和延伸因子 NusA 和 NusG 形成特定的“预终止复合物”(PTC),从而稳定 PTC。从环的远端 C 端进入 Rho 的中央通道之前,从 RNAP 中出来的 RNA 与 NusA 相互作用。我们绘制了 PTC 中的主要相互作用图,并证明了它们在终止中的关键作用。我们的结果支持这样一种机制,即形成持久的 PTC 是终止的先决条件。