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细菌转录泡形成的一般机制。

A general mechanism for transcription bubble nucleation in bacteria.

机构信息

Laboratory of Molecular Biophysics, The Rockefeller University, New York, NY 10065.

Department of Biochemistry and Molecular Biology, Penn State University, University Park, PA 16802.

出版信息

Proc Natl Acad Sci U S A. 2023 Apr 4;120(14):e2220874120. doi: 10.1073/pnas.2220874120. Epub 2023 Mar 27.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdf3/10083551/429444f59d0b/pnas.2220874120fig01.jpg

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