Laboratory of Molecular Biophysics, The Rockefeller University, New York, NY 10065.
Department of Biochemistry and Molecular Biology, Penn State University, University Park, PA 16802.
Proc Natl Acad Sci U S A. 2023 Apr 4;120(14):e2220874120. doi: 10.1073/pnas.2220874120. Epub 2023 Mar 27.
Bacterial transcription initiation requires σ factors for nucleation of the transcription bubble. The canonical housekeeping σ factor, σ, nucleates DNA melting via recognition of conserved bases of the promoter -10 motif, which are unstacked and captured in pockets of σ. By contrast, the mechanism of transcription bubble nucleation and formation during the unrelated σ-mediated transcription initiation is poorly understood. Herein, we combine structural and biochemical approaches to establish that σ, like σ, captures a flipped, unstacked base in a pocket formed between its N-terminal region I (RI) and extra-long helix features. Strikingly, RI inserts into the nascent bubble to stabilize the nucleated bubble prior to engagement of the obligate ATPase activator. Our data suggest a general paradigm of transcription initiation that requires σ factors to nucleate an early melted intermediate prior to productive RNA synthesis.
细菌转录起始需要 σ 因子来引发转录泡的形成。典型的管家 σ 因子 σ 通过识别启动子-10 基序的保守碱基来引发 DNA 熔解,这些碱基被解链并被 σ 因子的口袋捕获。相比之下,在不相关的 σ 介导的转录起始过程中,转录泡的形成机制还知之甚少。在此,我们结合结构和生化方法来确定 σ 就像 σ 一样,在其 N 端区域 I(RI)和超长螺旋特征之间形成的口袋中捕获一个翻转的、未堆叠的碱基。引人注目的是,RI 插入到新生的泡中,在必需的 ATP 酶激活剂结合之前稳定起始的泡。我们的数据表明,转录起始需要 σ 因子来引发早期的熔解中间产物,然后才能进行有效的 RNA 合成。