Cargando…

High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations

High-throughput sequencing has enabled genetic screens that can rapidly identify mutations that occur during experimental evolution. The presence of a mutation in an evolved lineage does not, however, constitute proof that the mutation is adaptive, given the well-known and widespread phenomenon of g...

Descripción completa

Detalles Bibliográficos
Autores principales: Payen, Celia, Sunshine, Anna B., Ong, Giang T., Pogachar, Jamie L., Zhao, Wei, Dunham, Maitreya J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065121/
https://www.ncbi.nlm.nih.gov/pubmed/27727276
http://dx.doi.org/10.1371/journal.pgen.1006339
_version_ 1782460269964820480
author Payen, Celia
Sunshine, Anna B.
Ong, Giang T.
Pogachar, Jamie L.
Zhao, Wei
Dunham, Maitreya J.
author_facet Payen, Celia
Sunshine, Anna B.
Ong, Giang T.
Pogachar, Jamie L.
Zhao, Wei
Dunham, Maitreya J.
author_sort Payen, Celia
collection PubMed
description High-throughput sequencing has enabled genetic screens that can rapidly identify mutations that occur during experimental evolution. The presence of a mutation in an evolved lineage does not, however, constitute proof that the mutation is adaptive, given the well-known and widespread phenomenon of genetic hitchhiking, in which a non-adaptive or even detrimental mutation can co-occur in a genome with a beneficial mutation and the combined genotype is carried to high frequency by selection. We approximated the spectrum of possible beneficial mutations in Saccharomyces cerevisiae using sets of single-gene deletions and amplifications of almost all the genes in the S. cerevisiae genome. We determined the fitness effects of each mutation in three different nutrient-limited conditions using pooled competitions followed by barcode sequencing. Although most of the mutations were neutral or deleterious, ~500 of them increased fitness. We then compared those results to the mutations that actually occurred during experimental evolution in the same three nutrient-limited conditions. On average, ~35% of the mutations that occurred during experimental evolution were predicted by the systematic screen to be beneficial. We found that the distribution of fitness effects depended on the selective conditions. In the phosphate-limited and glucose-limited conditions, a large number of beneficial mutations of nearly equivalent, small effects drove the fitness increases. In the sulfate-limited condition, one type of mutation, the amplification of the high-affinity sulfate transporter, dominated. In the absence of that mutation, evolution in the sulfate-limited condition involved mutations in other genes that were not observed previously—but were predicted by the systematic screen. Thus, gross functional screens have the potential to predict and identify adaptive mutations that occur during experimental evolution.
format Online
Article
Text
id pubmed-5065121
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-50651212016-10-27 High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations Payen, Celia Sunshine, Anna B. Ong, Giang T. Pogachar, Jamie L. Zhao, Wei Dunham, Maitreya J. PLoS Genet Research Article High-throughput sequencing has enabled genetic screens that can rapidly identify mutations that occur during experimental evolution. The presence of a mutation in an evolved lineage does not, however, constitute proof that the mutation is adaptive, given the well-known and widespread phenomenon of genetic hitchhiking, in which a non-adaptive or even detrimental mutation can co-occur in a genome with a beneficial mutation and the combined genotype is carried to high frequency by selection. We approximated the spectrum of possible beneficial mutations in Saccharomyces cerevisiae using sets of single-gene deletions and amplifications of almost all the genes in the S. cerevisiae genome. We determined the fitness effects of each mutation in three different nutrient-limited conditions using pooled competitions followed by barcode sequencing. Although most of the mutations were neutral or deleterious, ~500 of them increased fitness. We then compared those results to the mutations that actually occurred during experimental evolution in the same three nutrient-limited conditions. On average, ~35% of the mutations that occurred during experimental evolution were predicted by the systematic screen to be beneficial. We found that the distribution of fitness effects depended on the selective conditions. In the phosphate-limited and glucose-limited conditions, a large number of beneficial mutations of nearly equivalent, small effects drove the fitness increases. In the sulfate-limited condition, one type of mutation, the amplification of the high-affinity sulfate transporter, dominated. In the absence of that mutation, evolution in the sulfate-limited condition involved mutations in other genes that were not observed previously—but were predicted by the systematic screen. Thus, gross functional screens have the potential to predict and identify adaptive mutations that occur during experimental evolution. Public Library of Science 2016-10-11 /pmc/articles/PMC5065121/ /pubmed/27727276 http://dx.doi.org/10.1371/journal.pgen.1006339 Text en © 2016 Payen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Payen, Celia
Sunshine, Anna B.
Ong, Giang T.
Pogachar, Jamie L.
Zhao, Wei
Dunham, Maitreya J.
High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title_full High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title_fullStr High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title_full_unstemmed High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title_short High-Throughput Identification of Adaptive Mutations in Experimentally Evolved Yeast Populations
title_sort high-throughput identification of adaptive mutations in experimentally evolved yeast populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065121/
https://www.ncbi.nlm.nih.gov/pubmed/27727276
http://dx.doi.org/10.1371/journal.pgen.1006339
work_keys_str_mv AT payencelia highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations
AT sunshineannab highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations
AT onggiangt highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations
AT pogacharjamiel highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations
AT zhaowei highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations
AT dunhammaitreyaj highthroughputidentificationofadaptivemutationsinexperimentallyevolvedyeastpopulations