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Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location

BACKGROUND: Replication of bacterial chromosomes increases copy numbers of genes located near origins of replication relative to genes located near termini. Such differential gene dosage depends on replication rate, doubling time and chromosome size. Although little explored, differential gene dosag...

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Autores principales: Dryselius, Rikard, Izutsu, Kaori, Honda, Takeshi, Iida, Tetsuya
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612033/
https://www.ncbi.nlm.nih.gov/pubmed/19032792
http://dx.doi.org/10.1186/1471-2164-9-559
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author Dryselius, Rikard
Izutsu, Kaori
Honda, Takeshi
Iida, Tetsuya
author_facet Dryselius, Rikard
Izutsu, Kaori
Honda, Takeshi
Iida, Tetsuya
author_sort Dryselius, Rikard
collection PubMed
description BACKGROUND: Replication of bacterial chromosomes increases copy numbers of genes located near origins of replication relative to genes located near termini. Such differential gene dosage depends on replication rate, doubling time and chromosome size. Although little explored, differential gene dosage may influence both gene expression and location. For vibrios, a diverse family of fast growing gammaproteobacteria, gene dosage may be particularly important as they harbor two chromosomes of different size. RESULTS: Here we examined replication dynamics and gene dosage effects for the separate chromosomes of three Vibrio species. We also investigated locations for specific gene types within the genome. The results showed consistently larger gene dosage differences for the large chromosome which also initiated replication long before the small. Accordingly, large chromosome gene expression levels were generally higher and showed an influence from gene dosage. This was reflected by a higher abundance of growth essential and growth contributing genes of which many locate near the origin of replication. In contrast, small chromosome gene expression levels were low and appeared independent of gene dosage. Also, species specific genes are highly abundant and an over-representation of genes involved in transcription could explain its gene dosage independent expression. CONCLUSION: Here we establish a link between replication dynamics and differential gene dosage on one hand and gene expression levels and the location of specific gene types on the other. For vibrios, this relationship appears connected to a polarisation of genetic content between its chromosomes, which may both contribute to and be enhanced by an improved adaptive capacity.
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spelling pubmed-26120332009-01-12 Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location Dryselius, Rikard Izutsu, Kaori Honda, Takeshi Iida, Tetsuya BMC Genomics Research Article BACKGROUND: Replication of bacterial chromosomes increases copy numbers of genes located near origins of replication relative to genes located near termini. Such differential gene dosage depends on replication rate, doubling time and chromosome size. Although little explored, differential gene dosage may influence both gene expression and location. For vibrios, a diverse family of fast growing gammaproteobacteria, gene dosage may be particularly important as they harbor two chromosomes of different size. RESULTS: Here we examined replication dynamics and gene dosage effects for the separate chromosomes of three Vibrio species. We also investigated locations for specific gene types within the genome. The results showed consistently larger gene dosage differences for the large chromosome which also initiated replication long before the small. Accordingly, large chromosome gene expression levels were generally higher and showed an influence from gene dosage. This was reflected by a higher abundance of growth essential and growth contributing genes of which many locate near the origin of replication. In contrast, small chromosome gene expression levels were low and appeared independent of gene dosage. Also, species specific genes are highly abundant and an over-representation of genes involved in transcription could explain its gene dosage independent expression. CONCLUSION: Here we establish a link between replication dynamics and differential gene dosage on one hand and gene expression levels and the location of specific gene types on the other. For vibrios, this relationship appears connected to a polarisation of genetic content between its chromosomes, which may both contribute to and be enhanced by an improved adaptive capacity. BioMed Central 2008-11-26 /pmc/articles/PMC2612033/ /pubmed/19032792 http://dx.doi.org/10.1186/1471-2164-9-559 Text en Copyright © 2008 Dryselius et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dryselius, Rikard
Izutsu, Kaori
Honda, Takeshi
Iida, Tetsuya
Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title_full Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title_fullStr Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title_full_unstemmed Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title_short Differential replication dynamics for large and small Vibrio chromosomes affect gene dosage, expression and location
title_sort differential replication dynamics for large and small vibrio chromosomes affect gene dosage, expression and location
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2612033/
https://www.ncbi.nlm.nih.gov/pubmed/19032792
http://dx.doi.org/10.1186/1471-2164-9-559
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