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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |