TY - JOUR
T1 - Tempo and mode of genome evolution in a 50,000-generation experiment
AU - Tenaillon, Olivier
AU - Barrick, Jeffrey E.
AU - Ribeck, Noah
AU - Deatherage, Daniel E.
AU - Blanchard, Jeffrey L.
AU - Dasgupta, Aurko
AU - Wu, Gabriel C.
AU - Wielgoss, Sébastien
AU - Cruveiller, Stéphane
AU - Médigue, Claudine
AU - Schneider, Dominique
AU - Lenski, Richard E.
N1 - Publisher Copyright:
© 2016 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
PY - 2016/8/3
Y1 - 2016/8/3
N2 - Adaptation by natural selection depends on the rates, effects and interactions of many mutations, making it difficult to determine what proportion of mutations in an evolving lineage are beneficial. Here we analysed 264 complete genomes from 12 Escherichia coli populations to characterize their dynamics over 50,000 generations. The populations that retained the ancestral mutation rate support a model in which most fixed mutations are beneficial, the fraction of beneficial mutations declines as fitness rises, and neutral mutations accumulate at a constant rate. We also compared these populations to mutation-accumulation lines evolved under a bottlenecking regime that minimizes selection. Nonsynonymous mutations, intergenic mutations, insertions and deletions are overrepresented in the long-term populations, further supporting the inference that most mutations that reached high frequency were favoured by selection. These results illuminate the shifting balance of forces that govern genome evolution in populations adapting to a new environment.
AB - Adaptation by natural selection depends on the rates, effects and interactions of many mutations, making it difficult to determine what proportion of mutations in an evolving lineage are beneficial. Here we analysed 264 complete genomes from 12 Escherichia coli populations to characterize their dynamics over 50,000 generations. The populations that retained the ancestral mutation rate support a model in which most fixed mutations are beneficial, the fraction of beneficial mutations declines as fitness rises, and neutral mutations accumulate at a constant rate. We also compared these populations to mutation-accumulation lines evolved under a bottlenecking regime that minimizes selection. Nonsynonymous mutations, intergenic mutations, insertions and deletions are overrepresented in the long-term populations, further supporting the inference that most mutations that reached high frequency were favoured by selection. These results illuminate the shifting balance of forces that govern genome evolution in populations adapting to a new environment.
U2 - 10.1038/nature18959
DO - 10.1038/nature18959
M3 - Article
C2 - 27479321
AN - SCOPUS:84982085494
SN - 0028-0836
VL - 536
SP - 165
EP - 170
JO - Nature
JF - Nature
IS - 7615
ER -