Evidence map›Paper›PMID 27727276›Full record

ArticlePLoS genetics2016

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

Celia Payen, Anna B Sunshine, Giang T Ong, Jamie L Pogachar, Wei Zhao, Maitreya J Dunham

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Celia PayenDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Anna B SunshineDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID http://orcid.org/0000-0003-2456-6626
Giang T OngDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Jamie L PogacharDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Wei ZhaoDepartment of Biostatistics, University of Washington, Seattle, Washington, United States of America.
Maitreya J DunhamDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID http://orcid.org/0000-0001-9944-2666

Funding

University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
GENETIC APPROACHES TO AGING RESEARCHT32AG000057 · NIA · UNIVERSITY OF WASHINGTON · PI RABINOVITCH, PETER S · 1985 to 2019
$14.2M
Causes and consequences of gene copy number change in adapting yeast populationsR01GM094306 · NIGMS · UNIVERSITY OF WASHINGTON · PI DUNHAM, MAITREYA J · 2011 to 2015
$1.3M
Dissecting the genetic determinants of aneuploidy's effect on cellular proliferatF30CA165440 · NCI · UNIVERSITY OF WASHINGTON · PI SUNSHINE, ANNA BROSIUS · 2012 to 2013
$79k
NCI NIH HHS F30 CA165440NIA NIH HHS T32 AG000057NIGMS NIH HHS R01 GM094306NIGMS NIH HHS T32 GM007266
6 · The paper itself

Abstract

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.

Indexed as

Genetic FitnessSelection, GeneticAdaptation, PhysiologicalDirected Molecular EvolutionDNA Barcoding, TaxonomicGenotypeMutationSaccharomyces cerevisiae

Identifiers

PMID27727276
PMCPMC5065121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.