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A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq

Transcription initiation that involves the use of a 2- to ~4-nt oligoribonucleotide primer, “primer-dependent initiation,” (PDI) has been shown to be widely prevalent at promoters of genes expressed during the stationary phase of growth in Escherichia coli. However, the extent to which PDI impacts E...

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Autores principales: Druzhinin, Sergey Y., Tran, Ngat T., Skalenko, Kyle S., Goldman, Seth R., Knoblauch, Jared G., Dove, Simon L., Nickels, Bryce E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488433/
https://www.ncbi.nlm.nih.gov/pubmed/26131907
http://dx.doi.org/10.1371/journal.pgen.1005348
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author Druzhinin, Sergey Y.
Tran, Ngat T.
Skalenko, Kyle S.
Goldman, Seth R.
Knoblauch, Jared G.
Dove, Simon L.
Nickels, Bryce E.
author_facet Druzhinin, Sergey Y.
Tran, Ngat T.
Skalenko, Kyle S.
Goldman, Seth R.
Knoblauch, Jared G.
Dove, Simon L.
Nickels, Bryce E.
author_sort Druzhinin, Sergey Y.
collection PubMed
description Transcription initiation that involves the use of a 2- to ~4-nt oligoribonucleotide primer, “primer-dependent initiation,” (PDI) has been shown to be widely prevalent at promoters of genes expressed during the stationary phase of growth in Escherichia coli. However, the extent to which PDI impacts E. coli physiology, and the extent to which PDI occurs in other bacteria is not known. Here we establish a physiological role for PDI in E. coli as a regulatory mechanism that modulates biofilm formation. We further demonstrate using high-throughput sequencing of RNA 5′ ends (5′ RNA-seq) that PDI occurs in the pathogenic bacterium Vibrio cholerae. A comparative global analysis of PDI in V. cholerae and E. coli reveals that the pattern of PDI is strikingly similar in the two organisms. In particular, PDI is detected in stationary phase, is not detected in exponential phase, and is preferentially apparent at promoters carrying the sequence T(−1)A(+1) or G(−1)G(+1) (where position +1 corresponds to the position of de novo initiation). Our findings demonstrate a physiological role for PDI and suggest PDI may be widespread among Gammaproteobacteria. We propose that PDI in both E. coli and V. cholerae occurs though a growth phase-dependent process that leads to the preferential generation of the linear dinucleotides 5´-UA-3´ and 5´-GG-3´.
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spelling pubmed-44884332015-07-14 A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq Druzhinin, Sergey Y. Tran, Ngat T. Skalenko, Kyle S. Goldman, Seth R. Knoblauch, Jared G. Dove, Simon L. Nickels, Bryce E. PLoS Genet Research Article Transcription initiation that involves the use of a 2- to ~4-nt oligoribonucleotide primer, “primer-dependent initiation,” (PDI) has been shown to be widely prevalent at promoters of genes expressed during the stationary phase of growth in Escherichia coli. However, the extent to which PDI impacts E. coli physiology, and the extent to which PDI occurs in other bacteria is not known. Here we establish a physiological role for PDI in E. coli as a regulatory mechanism that modulates biofilm formation. We further demonstrate using high-throughput sequencing of RNA 5′ ends (5′ RNA-seq) that PDI occurs in the pathogenic bacterium Vibrio cholerae. A comparative global analysis of PDI in V. cholerae and E. coli reveals that the pattern of PDI is strikingly similar in the two organisms. In particular, PDI is detected in stationary phase, is not detected in exponential phase, and is preferentially apparent at promoters carrying the sequence T(−1)A(+1) or G(−1)G(+1) (where position +1 corresponds to the position of de novo initiation). Our findings demonstrate a physiological role for PDI and suggest PDI may be widespread among Gammaproteobacteria. We propose that PDI in both E. coli and V. cholerae occurs though a growth phase-dependent process that leads to the preferential generation of the linear dinucleotides 5´-UA-3´ and 5´-GG-3´. Public Library of Science 2015-07-01 /pmc/articles/PMC4488433/ /pubmed/26131907 http://dx.doi.org/10.1371/journal.pgen.1005348 Text en © 2015 Druzhinin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Druzhinin, Sergey Y.
Tran, Ngat T.
Skalenko, Kyle S.
Goldman, Seth R.
Knoblauch, Jared G.
Dove, Simon L.
Nickels, Bryce E.
A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title_full A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title_fullStr A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title_full_unstemmed A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title_short A Conserved Pattern of Primer-Dependent Transcription Initiation in Escherichia coli and Vibrio cholerae Revealed by 5′ RNA-seq
title_sort conserved pattern of primer-dependent transcription initiation in escherichia coli and vibrio cholerae revealed by 5′ rna-seq
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488433/
https://www.ncbi.nlm.nih.gov/pubmed/26131907
http://dx.doi.org/10.1371/journal.pgen.1005348
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