The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Mol Cell. 2018 Mar 1;69(5):802-815.e5. doi: 10.1016/j.molcel.2018.01.018.
Sequence-specific pausing by RNA polymerase (RNAP) during transcription plays crucial and diverse roles in gene expression. In bacteria, RNA structures are thought to fold within the RNA exit channel of the RNAP and can increase pause lifetimes significantly. The biophysical mechanism of pausing is uncertain. We used single-particle cryo-EM to determine structures of paused complexes, including a 3.8-Å structure of an RNA hairpin-stabilized, paused RNAP that coordinates RNA folding in the his operon attenuation control region of E. coli. The structures revealed a half-translocated pause state (RNA post-translocated, DNA pre-translocated) that can explain transcriptional pausing and a global conformational change of RNAP that allosterically inhibits trigger loop folding and can explain pause hairpin action. Pause hairpin interactions with the RNAP RNA exit channel suggest how RNAP guides the formation of nascent RNA structures.
RNA 聚合酶(RNAP)在转录过程中对 RNA 进行序列特异性暂停,在基因表达中发挥着关键且多样化的作用。在细菌中,RNA 结构被认为在 RNAP 的 RNA 出口通道内折叠,并能显著增加暂停寿命。暂停的生物物理机制尚不确定。我们使用单颗粒冷冻电镜确定了暂停复合物的结构,包括一个由 3.8 Å 分辨率的 RNA 发夹稳定的暂停 RNAP 结构,该结构协调了 E. coli 组氨酸操纵子衰减控制区中 RNA 的折叠。这些结构揭示了一个半移位暂停状态(RNA 后移位,DNA 前移位),可以解释转录暂停,以及 RNAP 的全局构象变化,这种变化别构抑制了触发环折叠,并可以解释暂停发夹的作用。暂停发夹与 RNAP RNA 出口通道的相互作用表明了 RNAP 如何引导新生 RNA 结构的形成。