Department of Integrated Structural Biology, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), 67404, Illkirch, France.
Université de Strasbourg, 67404, Illkirch, France.
Nat Commun. 2022 Mar 22;13(1):1546. doi: 10.1038/s41467-022-29148-0.
RNA polymerase (RNAP) frequently pauses during the transcription of DNA to RNA to regulate gene expression. Transcription factors NusA and NusG modulate pausing, have opposing roles, but can bind RNAP simultaneously. Here we report cryo-EM reconstructions of Escherichia coli RNAP bound to NusG, or NusA, or both. RNAP conformational changes, referred to as swivelling, correlate with transcriptional pausing. NusA facilitates RNAP swivelling to further increase pausing, while NusG counteracts this role. Their structural effects are consistent with biochemical results on two categories of transcriptional pauses. In addition, the structures suggest a cooperative mechanism of NusA and NusG during Rho-mediated transcription termination. Our results provide a structural rationale for the stochastic nature of pausing and termination and how NusA and NusG can modulate it.
RNA 聚合酶(RNAP)在将 DNA 转录为 RNA 以调节基因表达的过程中经常暂停。转录因子 NusA 和 NusG 调节暂停,具有相反的作用,但可以同时结合 RNAP。在这里,我们报告了与 NusG 或 NusA 或两者结合的大肠杆菌 RNAP 的冷冻电镜重建。称为旋转的 RNAP 构象变化与转录暂停相关。NusA 促进 RNAP 旋转以进一步增加暂停,而 NusG 则抵消了这种作用。它们的结构效应与关于两种转录暂停类别的生化结果一致。此外,这些结构表明了 Rho 介导的转录终止过程中 NusA 和 NusG 之间的合作机制。我们的结果为暂停和终止的随机性以及 NusA 和 NusG 如何调节它们提供了结构基础。