Dynamic insights on transcription initiation and RNA processing during bacterial adaptation
- Caroline Lacoux1,7,
- Aymeric Fouquier d'Hérouël2,
- Françoise Wessner-Le Bohec1,
- Nicolas Innocenti1,3,8,
- Chantal Bohn4,
- Sean P. Kennedy5,
- Tatiana Rochat6,
- Rémy A. Bonnin4,9,
- Pascale Serror1,
- Erik Aurell3,
- Philippe Bouloc4 and
- Francis Repoila1
- 1Université Paris-Saclay, INRAE, AgroParisTech, MIcalis Institute, 78350, Jouy-en-Josas, France
- 2Luxembourg Center for Systems Biomedicine, University of Luxembourg, 4367, Belvaux, Luxembourg
- 3Department of Computational Biology, Royal Institute of Technology, AlbaNova University Center, SE-10691 Stockholm, Sweden
- 4Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France
- 5Department of Computational Biology, USR3756 CNRS, Institut Pasteur, 75 015 Paris, France
- 6VIM, INRA, Université Paris-Saclay, 78350 Jouy-en-Josas, France
- Corresponding author: francis.repoila{at}inra.fr
Abstract
Transcription initiation and RNA processing govern gene expression and enable bacterial adaptation by reshaping the RNA landscape. The aim of this study was to simultaneously observe these two fundamental processes in a transcriptome responding to an environmental signal. A controlled σE system in E. coli was coupled to our previously described tagRNA-seq method to yield process kinetics information. Changes in transcription initiation frequencies (TIF) and RNA processing frequencies (PF) were followed using 5′ RNA tags. Changes in TIF showed a binary increased/decreased pattern that alternated between transcriptionally activated and repressed promoters, providing the bacterial population with transcriptional oscillation. PF variation fell into three categories of cleavage activity: (i) constant and independent of RNA levels, (ii) increased once RNA has accumulated, and (iii) positively correlated to changes in TIF. This work provides a comprehensive and dynamic view of major events leading to transcriptomic reshaping during bacterial adaptation. It unveils an interplay between transcription initiation and the activity of specific RNA cleavage sites. This study utilized a well-known genetic system to analyze fundamental processes and can serve as a blueprint for comprehensive studies that exploit the RNA metabolism to decipher and understand bacterial gene expression control.
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Article is online at http://www.rnajournal.org/cgi/doi/10.1261/rna.073288.119.
- Received September 11, 2019.
- Accepted January 20, 2020.
This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.










