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Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting

BACKGROUND: Gene duplication is believed to be the classical way to form novel genes, but overprinting may be an important alternative. Overprinting allows entirely novel proteins to evolve de novo, i.e., formerly non-coding open reading frames within functional genes become expressed. Only three ca...

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Autores principales: Fellner, Lea, Simon, Svenja, Scherling, Christian, Witting, Michael, Schober, Steffen, Polte, Christine, Schmitt-Kopplin, Philippe, Keim, Daniel A., Scherer, Siegfried, Neuhaus, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683798/
https://www.ncbi.nlm.nih.gov/pubmed/26677845
http://dx.doi.org/10.1186/s12862-015-0558-z
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author Fellner, Lea
Simon, Svenja
Scherling, Christian
Witting, Michael
Schober, Steffen
Polte, Christine
Schmitt-Kopplin, Philippe
Keim, Daniel A.
Scherer, Siegfried
Neuhaus, Klaus
author_facet Fellner, Lea
Simon, Svenja
Scherling, Christian
Witting, Michael
Schober, Steffen
Polte, Christine
Schmitt-Kopplin, Philippe
Keim, Daniel A.
Scherer, Siegfried
Neuhaus, Klaus
author_sort Fellner, Lea
collection PubMed
description BACKGROUND: Gene duplication is believed to be the classical way to form novel genes, but overprinting may be an important alternative. Overprinting allows entirely novel proteins to evolve de novo, i.e., formerly non-coding open reading frames within functional genes become expressed. Only three cases have been described for Escherichia coli. Here, a fourth example is presented. RESULTS: RNA sequencing revealed an open reading frame weakly transcribed in cow dung, coding for 101 residues and embedded completely in the −2 reading frame of citC in enterohemorrhagic E. coli. This gene is designated novel overlapping gene, nog1. The promoter region fused to gfp exhibits specific activities and 5’ rapid amplification of cDNA ends indicated the transcriptional start 40-bp upstream of the start codon. nog1 was strand-specifically arrested in translation by a nonsense mutation silent in citC. This Nog1-mutant showed a phenotype in competitive growth against wild type in the presence of MgCl(2). Small differences in metabolite concentrations were also found. Bioinformatic analyses propose Nog1 to be inner membrane-bound and to possess at least one membrane-spanning domain. A phylogenetic analysis suggests that the orphan gene nog1 arose by overprinting after Escherichia/Shigella separated from the other γ-proteobacteria. CONCLUSIONS: Since nog1 is of recent origin, non-essential, short, weakly expressed and only marginally involved in E. coli’s central metabolism, we propose that this gene is in an initial stage of evolution. While we present specific experimental evidence for the existence of a fourth overlapping gene in enterohemorrhagic E. coli, we believe that this may be an initial finding only and overlapping genes in bacteria may be more common than is currently assumed by microbiologists. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0558-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-46837982015-12-19 Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting Fellner, Lea Simon, Svenja Scherling, Christian Witting, Michael Schober, Steffen Polte, Christine Schmitt-Kopplin, Philippe Keim, Daniel A. Scherer, Siegfried Neuhaus, Klaus BMC Evol Biol Research Article BACKGROUND: Gene duplication is believed to be the classical way to form novel genes, but overprinting may be an important alternative. Overprinting allows entirely novel proteins to evolve de novo, i.e., formerly non-coding open reading frames within functional genes become expressed. Only three cases have been described for Escherichia coli. Here, a fourth example is presented. RESULTS: RNA sequencing revealed an open reading frame weakly transcribed in cow dung, coding for 101 residues and embedded completely in the −2 reading frame of citC in enterohemorrhagic E. coli. This gene is designated novel overlapping gene, nog1. The promoter region fused to gfp exhibits specific activities and 5’ rapid amplification of cDNA ends indicated the transcriptional start 40-bp upstream of the start codon. nog1 was strand-specifically arrested in translation by a nonsense mutation silent in citC. This Nog1-mutant showed a phenotype in competitive growth against wild type in the presence of MgCl(2). Small differences in metabolite concentrations were also found. Bioinformatic analyses propose Nog1 to be inner membrane-bound and to possess at least one membrane-spanning domain. A phylogenetic analysis suggests that the orphan gene nog1 arose by overprinting after Escherichia/Shigella separated from the other γ-proteobacteria. CONCLUSIONS: Since nog1 is of recent origin, non-essential, short, weakly expressed and only marginally involved in E. coli’s central metabolism, we propose that this gene is in an initial stage of evolution. While we present specific experimental evidence for the existence of a fourth overlapping gene in enterohemorrhagic E. coli, we believe that this may be an initial finding only and overlapping genes in bacteria may be more common than is currently assumed by microbiologists. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0558-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-18 /pmc/articles/PMC4683798/ /pubmed/26677845 http://dx.doi.org/10.1186/s12862-015-0558-z Text en © Fellner et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fellner, Lea
Simon, Svenja
Scherling, Christian
Witting, Michael
Schober, Steffen
Polte, Christine
Schmitt-Kopplin, Philippe
Keim, Daniel A.
Scherer, Siegfried
Neuhaus, Klaus
Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title_full Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title_fullStr Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title_full_unstemmed Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title_short Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
title_sort evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683798/
https://www.ncbi.nlm.nih.gov/pubmed/26677845
http://dx.doi.org/10.1186/s12862-015-0558-z
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