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A multivariate prediction model for Rho-dependent termination of transcription
Bacterial transcription termination proceeds via two main mechanisms triggered either by simple, well-conserved (intrinsic) nucleic acid motifs or by the motor protein Rho. Although bacterial genomes can harbor hundreds of termination signals of either type, only intrinsic terminators are reliably p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144790/ https://www.ncbi.nlm.nih.gov/pubmed/29931073 http://dx.doi.org/10.1093/nar/gky563 |
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author | Nadiras, Cédric Eveno, Eric Schwartz, Annie Figueroa-Bossi, Nara Boudvillain, Marc |
author_facet | Nadiras, Cédric Eveno, Eric Schwartz, Annie Figueroa-Bossi, Nara Boudvillain, Marc |
author_sort | Nadiras, Cédric |
collection | PubMed |
description | Bacterial transcription termination proceeds via two main mechanisms triggered either by simple, well-conserved (intrinsic) nucleic acid motifs or by the motor protein Rho. Although bacterial genomes can harbor hundreds of termination signals of either type, only intrinsic terminators are reliably predicted. Computational tools to detect the more complex and diversiform Rho-dependent terminators are lacking. To tackle this issue, we devised a prediction method based on Orthogonal Projections to Latent Structures Discriminant Analysis [OPLS-DA] of a large set of in vitro termination data. Using previously uncharacterized genomic sequences for biochemical evaluation and OPLS-DA, we identified new Rho-dependent signals and quantitative sequence descriptors with significant predictive value. Most relevant descriptors specify features of transcript C>G skewness, secondary structure, and richness in regularly-spaced 5′CC/UC dinucleotides that are consistent with known principles for Rho-RNA interaction. Descriptors collectively warrant OPLS-DA predictions of Rho-dependent termination with a ∼85% success rate. Scanning of the Escherichia coli genome with the OPLS-DA model identifies significantly more termination-competent regions than anticipated from transcriptomics and predicts that regions intrinsically refractory to Rho are primarily located in open reading frames. Altogether, this work delineates features important for Rho activity and describes the first method able to predict Rho-dependent terminators in bacterial genomes. |
format | Online Article Text |
id | pubmed-6144790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61447902018-09-25 A multivariate prediction model for Rho-dependent termination of transcription Nadiras, Cédric Eveno, Eric Schwartz, Annie Figueroa-Bossi, Nara Boudvillain, Marc Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Bacterial transcription termination proceeds via two main mechanisms triggered either by simple, well-conserved (intrinsic) nucleic acid motifs or by the motor protein Rho. Although bacterial genomes can harbor hundreds of termination signals of either type, only intrinsic terminators are reliably predicted. Computational tools to detect the more complex and diversiform Rho-dependent terminators are lacking. To tackle this issue, we devised a prediction method based on Orthogonal Projections to Latent Structures Discriminant Analysis [OPLS-DA] of a large set of in vitro termination data. Using previously uncharacterized genomic sequences for biochemical evaluation and OPLS-DA, we identified new Rho-dependent signals and quantitative sequence descriptors with significant predictive value. Most relevant descriptors specify features of transcript C>G skewness, secondary structure, and richness in regularly-spaced 5′CC/UC dinucleotides that are consistent with known principles for Rho-RNA interaction. Descriptors collectively warrant OPLS-DA predictions of Rho-dependent termination with a ∼85% success rate. Scanning of the Escherichia coli genome with the OPLS-DA model identifies significantly more termination-competent regions than anticipated from transcriptomics and predicts that regions intrinsically refractory to Rho are primarily located in open reading frames. Altogether, this work delineates features important for Rho activity and describes the first method able to predict Rho-dependent terminators in bacterial genomes. Oxford University Press 2018-09-19 2018-06-21 /pmc/articles/PMC6144790/ /pubmed/29931073 http://dx.doi.org/10.1093/nar/gky563 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Nadiras, Cédric Eveno, Eric Schwartz, Annie Figueroa-Bossi, Nara Boudvillain, Marc A multivariate prediction model for Rho-dependent termination of transcription |
title | A multivariate prediction model for Rho-dependent termination of transcription |
title_full | A multivariate prediction model for Rho-dependent termination of transcription |
title_fullStr | A multivariate prediction model for Rho-dependent termination of transcription |
title_full_unstemmed | A multivariate prediction model for Rho-dependent termination of transcription |
title_short | A multivariate prediction model for Rho-dependent termination of transcription |
title_sort | multivariate prediction model for rho-dependent termination of transcription |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144790/ https://www.ncbi.nlm.nih.gov/pubmed/29931073 http://dx.doi.org/10.1093/nar/gky563 |
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