Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>

<p>Abstract</p> <p>Background</p> <p>Twelve populations of <it>E. coli </it>were serially propagated for 20,000 generations in a glucose-supplemented minimal medium in order to study the dynamics of evolution. We sought to find and characterize one of the be...

Full description

Bibliographic Details
Main Authors: Lenski Richard E, Cooper Tim F, Stanek Mark T
Format: Article
Language:English
Published: BMC 2009-12-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/9/302
id doaj-f128b0773b7648268d00564f36d5213f
record_format Article
spelling doaj-f128b0773b7648268d00564f36d5213f2021-09-02T08:16:43ZengBMCBMC Evolutionary Biology1471-21482009-12-019130210.1186/1471-2148-9-302Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>Lenski Richard ECooper Tim FStanek Mark T<p>Abstract</p> <p>Background</p> <p>Twelve populations of <it>E. coli </it>were serially propagated for 20,000 generations in a glucose-supplemented minimal medium in order to study the dynamics of evolution. We sought to find and characterize one of the beneficial mutations responsible for the adaptation and other phenotypic changes, including increased cell size, in one of these populations.</p> <p>Results</p> <p>We used transposon-tagging followed by P1-transduction into the ancestor, screening for increased cell size and fitness, co-transduction analysis, and DNA sequencing. We identified a 1-bp insertion in the BoxG1 region located upstream of <it>glmUS</it>, an operon involved in cell-wall biosynthesis. When transduced into the ancestor, this mutation increased competitive fitness by about 5%. This mutation spread through its population of origin between 500 and 1500 generations. Mutations in this region were not found in the other 11 evolving populations, even after 20,000 generations.</p> <p>Conclusion</p> <p>The 1-bp insertion in the BoxG1 region near <it>glmUS </it>was demonstrably beneficial in the environment in which it arose. The absence of similar mutations in the other evolved populations suggests that they substituted other mutations that rendered this particular mutation unimportant. These results show the unpredictability of adaptive evolution, whereas parallel substitutions at other loci in these same populations reveal the predictability.</p> http://www.biomedcentral.com/1471-2148/9/302
collection DOAJ
language English
format Article
sources DOAJ
author Lenski Richard E
Cooper Tim F
Stanek Mark T
spellingShingle Lenski Richard E
Cooper Tim F
Stanek Mark T
Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
BMC Evolutionary Biology
author_facet Lenski Richard E
Cooper Tim F
Stanek Mark T
author_sort Lenski Richard E
title Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
title_short Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
title_full Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
title_fullStr Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
title_full_unstemmed Identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>Escherichia coli</it>
title_sort identification and dynamics of a beneficial mutation in a long-term evolution experiment with <it>escherichia coli</it>
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2009-12-01
description <p>Abstract</p> <p>Background</p> <p>Twelve populations of <it>E. coli </it>were serially propagated for 20,000 generations in a glucose-supplemented minimal medium in order to study the dynamics of evolution. We sought to find and characterize one of the beneficial mutations responsible for the adaptation and other phenotypic changes, including increased cell size, in one of these populations.</p> <p>Results</p> <p>We used transposon-tagging followed by P1-transduction into the ancestor, screening for increased cell size and fitness, co-transduction analysis, and DNA sequencing. We identified a 1-bp insertion in the BoxG1 region located upstream of <it>glmUS</it>, an operon involved in cell-wall biosynthesis. When transduced into the ancestor, this mutation increased competitive fitness by about 5%. This mutation spread through its population of origin between 500 and 1500 generations. Mutations in this region were not found in the other 11 evolving populations, even after 20,000 generations.</p> <p>Conclusion</p> <p>The 1-bp insertion in the BoxG1 region near <it>glmUS </it>was demonstrably beneficial in the environment in which it arose. The absence of similar mutations in the other evolved populations suggests that they substituted other mutations that rendered this particular mutation unimportant. These results show the unpredictability of adaptive evolution, whereas parallel substitutions at other loci in these same populations reveal the predictability.</p>
url http://www.biomedcentral.com/1471-2148/9/302
work_keys_str_mv AT lenskiricharde identificationanddynamicsofabeneficialmutationinalongtermevolutionexperimentwithitescherichiacoliit
AT coopertimf identificationanddynamicsofabeneficialmutationinalongtermevolutionexperimentwithitescherichiacoliit
AT stanekmarkt identificationanddynamicsofabeneficialmutationinalongtermevolutionexperimentwithitescherichiacoliit
_version_ 1721177915657289728