Cargando…

Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation

Recent studies strongly suggest that in bacteria, both the genomic pattern of DNA thermodynamic stability and the order of genes along the chromosomal origin-to-terminus axis are highly conserved and that this spatial organization plays a crucial role in coordinating genomic transcription. In this a...

Descripción completa

Detalles Bibliográficos
Autores principales: Muskhelishvili, Georgi, Forquet, Raphaël, Reverchon, Sylvie, Meyer, Sam, Nasser, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956064/
https://www.ncbi.nlm.nih.gov/pubmed/31847191
http://dx.doi.org/10.3390/microorganisms7120694
_version_ 1783487074183151616
author Muskhelishvili, Georgi
Forquet, Raphaël
Reverchon, Sylvie
Meyer, Sam
Nasser, William
author_facet Muskhelishvili, Georgi
Forquet, Raphaël
Reverchon, Sylvie
Meyer, Sam
Nasser, William
author_sort Muskhelishvili, Georgi
collection PubMed
description Recent studies strongly suggest that in bacteria, both the genomic pattern of DNA thermodynamic stability and the order of genes along the chromosomal origin-to-terminus axis are highly conserved and that this spatial organization plays a crucial role in coordinating genomic transcription. In this article, we explore the relationship between genomic sequence organization and transcription in the commensal bacterium Escherichia coli and the plant pathogen Dickeya. We argue that, while in E. coli the gradient of DNA thermodynamic stability and gene order along the origin-to-terminus axis represent major organizational features orchestrating temporal gene expression, the genomic sequence organization of Dickeya is more complex, demonstrating extended chromosomal domains of thermodynamically distinct DNA sequences eliciting specific transcriptional responses to various kinds of stress encountered during pathogenic growth. This feature of the Dickeya genome is likely an adaptation to the pathogenic lifestyle utilizing differences in genomic sequence organization for the selective expression of virulence traits. We propose that the coupling of DNA thermodynamic stability and genetic function provides a common organizational principle for the coordinated expression of genes during both normal and pathogenic bacterial growth.
format Online
Article
Text
id pubmed-6956064
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-69560642020-01-23 Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation Muskhelishvili, Georgi Forquet, Raphaël Reverchon, Sylvie Meyer, Sam Nasser, William Microorganisms Review Recent studies strongly suggest that in bacteria, both the genomic pattern of DNA thermodynamic stability and the order of genes along the chromosomal origin-to-terminus axis are highly conserved and that this spatial organization plays a crucial role in coordinating genomic transcription. In this article, we explore the relationship between genomic sequence organization and transcription in the commensal bacterium Escherichia coli and the plant pathogen Dickeya. We argue that, while in E. coli the gradient of DNA thermodynamic stability and gene order along the origin-to-terminus axis represent major organizational features orchestrating temporal gene expression, the genomic sequence organization of Dickeya is more complex, demonstrating extended chromosomal domains of thermodynamically distinct DNA sequences eliciting specific transcriptional responses to various kinds of stress encountered during pathogenic growth. This feature of the Dickeya genome is likely an adaptation to the pathogenic lifestyle utilizing differences in genomic sequence organization for the selective expression of virulence traits. We propose that the coupling of DNA thermodynamic stability and genetic function provides a common organizational principle for the coordinated expression of genes during both normal and pathogenic bacterial growth. MDPI 2019-12-13 /pmc/articles/PMC6956064/ /pubmed/31847191 http://dx.doi.org/10.3390/microorganisms7120694 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Muskhelishvili, Georgi
Forquet, Raphaël
Reverchon, Sylvie
Meyer, Sam
Nasser, William
Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title_full Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title_fullStr Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title_full_unstemmed Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title_short Coherent Domains of Transcription Coordinate Gene Expression During Bacterial Growth and Adaptation
title_sort coherent domains of transcription coordinate gene expression during bacterial growth and adaptation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956064/
https://www.ncbi.nlm.nih.gov/pubmed/31847191
http://dx.doi.org/10.3390/microorganisms7120694
work_keys_str_mv AT muskhelishviligeorgi coherentdomainsoftranscriptioncoordinategeneexpressionduringbacterialgrowthandadaptation
AT forquetraphael coherentdomainsoftranscriptioncoordinategeneexpressionduringbacterialgrowthandadaptation
AT reverchonsylvie coherentdomainsoftranscriptioncoordinategeneexpressionduringbacterialgrowthandadaptation
AT meyersam coherentdomainsoftranscriptioncoordinategeneexpressionduringbacterialgrowthandadaptation
AT nasserwilliam coherentdomainsoftranscriptioncoordinategeneexpressionduringbacterialgrowthandadaptation