4.8 Article

Basic mechanisms and kinetics of pause-interspersed transcript elongation

Journal

NUCLEIC ACIDS RESEARCH
Volume 49, Issue 1, Pages 15-24

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkaa1182

Keywords

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Funding

  1. National Institutes of Health (NIH) [R01 GM084070]
  2. NIGMS [R01GM084070]

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RNA polymerase pausing during elongation is an important mechanism in the regulation of gene expression. The signals inducing pausing are thought to be encoded in the nucleic acid sequence, causing elongation complexes to temporarily halt for co-transcriptional events. Recent advances in structural microbiology and single-molecule studies have enhanced our understanding of paused states, but the dynamics of these states are still unclear, with multiple proposed models to explain experimental observations.
RNA polymerase pausing during elongation is an important mechanism in the regulation of gene expression. Pausing along DNA templates is thought to be induced by distinct signals encoded in the nucleic acid sequence and halt elongation complexes to allow time for necessary co-transcriptional events. Pausing signals have been classified as those producing short-lived elemental, long-lived backtracked, or hairpin-stabilized pauses. In recent years, structural microbiology and single-molecule studies have significantly advanced our understanding of the paused states, but the dynamics of these states are still uncertain, although several models have been proposed to explain the experimentally observed pausing behaviors. This review summarizes present knowledge about the paused states, discusses key discrepancies among the kinetic models and their basic assumptions, and highlights the importance and challenges in constructing theoretical models that may further our biochemical understanding of transcriptional pausing.

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