AI Article Synopsis

  • - Sequence-specific pausing by RNA polymerase (RNAP) is vital for gene expression, with RNA structures causing significant pauses during transcription in bacteria.
  • - Researchers used single-particle cryo-electron microscopy (cryo-EM) to analyze paused RNAP complexes, revealing structures that illustrate how RNA folding influences these pauses in E. coli.
  • - The study found that a unique half-translocated pause state of RNAP impacts both transcription pausing and the folding of the trigger loop, showing how RNAP helps form RNA structures as the transcript is produced.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903582PMC
http://dx.doi.org/10.1016/j.molcel.2018.01.018DOI Listing

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