Cargando…

Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli

Large-scale rearrangements may be important in evolution because they can alter chromosome organization and gene expression in ways not possible through point mutations. In a long-term evolution experiment, twelve Escherichia coli populations have been propagated in a glucose-limited environment for...

Descripción completa

Detalles Bibliográficos
Autores principales: Raeside, Colin, Gaffé, Joël, Deatherage, Daniel E., Tenaillon, Olivier, Briska, Adam M., Ptashkin, Ryan N., Cruveiller, Stéphane, Médigue, Claudine, Lenski, Richard E., Barrick, Jeffrey E., Schneider, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173774/
https://www.ncbi.nlm.nih.gov/pubmed/25205090
http://dx.doi.org/10.1128/mBio.01377-14
_version_ 1782336258169634816
author Raeside, Colin
Gaffé, Joël
Deatherage, Daniel E.
Tenaillon, Olivier
Briska, Adam M.
Ptashkin, Ryan N.
Cruveiller, Stéphane
Médigue, Claudine
Lenski, Richard E.
Barrick, Jeffrey E.
Schneider, Dominique
author_facet Raeside, Colin
Gaffé, Joël
Deatherage, Daniel E.
Tenaillon, Olivier
Briska, Adam M.
Ptashkin, Ryan N.
Cruveiller, Stéphane
Médigue, Claudine
Lenski, Richard E.
Barrick, Jeffrey E.
Schneider, Dominique
author_sort Raeside, Colin
collection PubMed
description Large-scale rearrangements may be important in evolution because they can alter chromosome organization and gene expression in ways not possible through point mutations. In a long-term evolution experiment, twelve Escherichia coli populations have been propagated in a glucose-limited environment for over 25 years. We used whole-genome mapping (optical mapping) combined with genome sequencing and PCR analysis to identify the large-scale chromosomal rearrangements in clones from each population after 40,000 generations. A total of 110 rearrangement events were detected, including 82 deletions, 19 inversions, and 9 duplications, with lineages having between 5 and 20 events. In three populations, successive rearrangements impacted particular regions. In five populations, rearrangements affected over a third of the chromosome. Most rearrangements involved recombination between insertion sequence (IS) elements, illustrating their importance in mediating genome plasticity. Two lines of evidence suggest that at least some of these rearrangements conferred higher fitness. First, parallel changes were observed across the independent populations, with ~65% of the rearrangements affecting the same loci in at least two populations. For example, the ribose-utilization operon and the manB-cpsG region were deleted in 12 and 10 populations, respectively, suggesting positive selection, and this inference was previously confirmed for the former case. Second, optical maps from clones sampled over time from one population showed that most rearrangements occurred early in the experiment, when fitness was increasing most rapidly. However, some rearrangements likely occur at high frequency and may have simply hitchhiked to fixation. In any case, large-scale rearrangements clearly influenced genomic evolution in these populations.
format Online
Article
Text
id pubmed-4173774
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher American Society of Microbiology
record_format MEDLINE/PubMed
spelling pubmed-41737742014-10-06 Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli Raeside, Colin Gaffé, Joël Deatherage, Daniel E. Tenaillon, Olivier Briska, Adam M. Ptashkin, Ryan N. Cruveiller, Stéphane Médigue, Claudine Lenski, Richard E. Barrick, Jeffrey E. Schneider, Dominique mBio Research Article Large-scale rearrangements may be important in evolution because they can alter chromosome organization and gene expression in ways not possible through point mutations. In a long-term evolution experiment, twelve Escherichia coli populations have been propagated in a glucose-limited environment for over 25 years. We used whole-genome mapping (optical mapping) combined with genome sequencing and PCR analysis to identify the large-scale chromosomal rearrangements in clones from each population after 40,000 generations. A total of 110 rearrangement events were detected, including 82 deletions, 19 inversions, and 9 duplications, with lineages having between 5 and 20 events. In three populations, successive rearrangements impacted particular regions. In five populations, rearrangements affected over a third of the chromosome. Most rearrangements involved recombination between insertion sequence (IS) elements, illustrating their importance in mediating genome plasticity. Two lines of evidence suggest that at least some of these rearrangements conferred higher fitness. First, parallel changes were observed across the independent populations, with ~65% of the rearrangements affecting the same loci in at least two populations. For example, the ribose-utilization operon and the manB-cpsG region were deleted in 12 and 10 populations, respectively, suggesting positive selection, and this inference was previously confirmed for the former case. Second, optical maps from clones sampled over time from one population showed that most rearrangements occurred early in the experiment, when fitness was increasing most rapidly. However, some rearrangements likely occur at high frequency and may have simply hitchhiked to fixation. In any case, large-scale rearrangements clearly influenced genomic evolution in these populations. American Society of Microbiology 2014-09-09 /pmc/articles/PMC4173774/ /pubmed/25205090 http://dx.doi.org/10.1128/mBio.01377-14 Text en Copyright © 2014 Raeside et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Raeside, Colin
Gaffé, Joël
Deatherage, Daniel E.
Tenaillon, Olivier
Briska, Adam M.
Ptashkin, Ryan N.
Cruveiller, Stéphane
Médigue, Claudine
Lenski, Richard E.
Barrick, Jeffrey E.
Schneider, Dominique
Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title_full Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title_fullStr Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title_full_unstemmed Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title_short Large Chromosomal Rearrangements during a Long-Term Evolution Experiment with Escherichia coli
title_sort large chromosomal rearrangements during a long-term evolution experiment with escherichia coli
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173774/
https://www.ncbi.nlm.nih.gov/pubmed/25205090
http://dx.doi.org/10.1128/mBio.01377-14
work_keys_str_mv AT raesidecolin largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT gaffejoel largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT deatheragedaniele largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT tenaillonolivier largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT briskaadamm largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT ptashkinryann largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT cruveillerstephane largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT medigueclaudine largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT lenskiricharde largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT barrickjeffreye largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli
AT schneiderdominique largechromosomalrearrangementsduringalongtermevolutionexperimentwithescherichiacoli