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Global repositioning of transcription start sites in a plant-fermenting bacterium

Magali Boutard, Laurence Ettwiller, Tristan Cerisy, Adriana Alberti, Karine Labadie, Marcel Salanoubat, Ira Schildkraut and Andrew C. Tolonen ()
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Magali Boutard: 1CEA, DRF, IG, Genoscope
Laurence Ettwiller: New England Biolabs, Inc.
Tristan Cerisy: 1CEA, DRF, IG, Genoscope
Adriana Alberti: 1CEA, DRF, IG, Genoscope
Karine Labadie: 1CEA, DRF, IG, Genoscope
Marcel Salanoubat: 1CEA, DRF, IG, Genoscope
Ira Schildkraut: New England Biolabs, Inc.
Andrew C. Tolonen: 1CEA, DRF, IG, Genoscope

Nature Communications, 2016, vol. 7, issue 1, 1-9

Abstract: Abstract Bacteria respond to their environment by regulating mRNA synthesis, often by altering the genomic sites at which RNA polymerase initiates transcription. Here, we investigate genome-wide changes in transcription start site (TSS) usage by Clostridium phytofermentans, a model bacterium for fermentation of lignocellulosic biomass. We quantify expression of nearly 10,000 TSS at single base resolution by Capp-Switch sequencing, which combines capture of synthetically capped 5′ mRNA fragments with template-switching reverse transcription. We find the locations and expression levels of TSS for hundreds of genes change during metabolism of different plant substrates. We show that TSS reveals riboswitches, non-coding RNA and novel transcription units. We identify sequence motifs associated with carbon source-specific TSS and use them for regulon discovery, implicating a LacI/GalR protein in control of pectin metabolism. We discuss how the high resolution and specificity of Capp-Switch enables study of condition-specific changes in transcription initiation in bacteria.

Date: 2016
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13783

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DOI: 10.1038/ncomms13783

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