Evidence map›Paper›PMID 28196070›Full record

ArticlePLoS genetics2017

Differential paralog divergence modulates genome evolution across yeast species.

Monica R Sanchez, Aaron W Miller, Ivan Liachko, Anna B Sunshine, Bryony Lynch, Mei Huang, Erica Alcantara, Christopher G DeSevo, Dave A Pai, Cheryl M Tucker and 2 more

Abstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  14. Loss of Heterozygosity Drives Adaptation in Hybrid Yeast.Molecular biology and evolution · 2017
    Article
  15. Article
  16. Article
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

12 authors.

Monica R SanchezDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0003-4413-9058
Aaron W MillerDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-5037-9539
Ivan LiachkoDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-6972-6705
Anna B SunshineDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0003-2456-6626
Bryony LynchDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Mei HuangDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Erica AlcantaraDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Christopher G DeSevoLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey, United States of America.
Dave A PaiLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey, United States of America.
Cheryl M TuckerLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey, United States of America.ORCID 0000-0003-2967-7448
Margaret L HoangHoward Hughes Medical Institute and Department of Embryology, Carnegie Institution, Baltimore, Maryland, United States of America.
Maitreya J DunhamDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0001-9944-2666

Funding

Spatial Patterning During DevelopmentP50GM071508 · NIGMS · PRINCETON UNIVERSITY · PI GAMMIE, ALISON E · 2004 to 2013
$30.6M
University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
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
Howard Hughes Medical InstituteNIGMS NIH HHS P50 GM071508NIGMS NIH HHS R01 GM094306NIGMS NIH HHS T32 GM007266
6 · The paper itself

Abstract

Evolutionary outcomes depend not only on the selective forces acting upon a species, but also on the genetic background. However, large timescales and uncertain historical selection pressures can make it difficult to discern such important background differences between species. Experimental evolution is one tool to compare evolutionary potential of known genotypes in a controlled environment. Here we utilized a highly reproducible evolutionary adaptation in Saccharomyces cerevisiae to investigate whether experimental evolution of other yeast species would select for similar adaptive mutations. We evolved populations of S. cerevisiae, S. paradoxus, S. mikatae, S. uvarum, and interspecific hybrids between S. uvarum and S. cerevisiae for ~200-500 generations in sulfate-limited continuous culture. Wild-type S. cerevisiae cultures invariably amplify the high affinity sulfate transporter gene, SUL1. However, while amplification of the SUL1 locus was detected in S. paradoxus and S. mikatae populations, S. uvarum cultures instead selected for amplification of the paralog, SUL2. We measured the relative fitness of strains bearing deletions and amplifications of both SUL genes from different species, confirming that, converse to S. cerevisiae, S. uvarum SUL2 contributes more to fitness in sulfate limitation than S. uvarum SUL1. By measuring the fitness and gene expression of chimeric promoter-ORF constructs, we were able to delineate the cause of this differential fitness effect primarily to the promoter of S. uvarum SUL1. Our data show evidence of differential sub-functionalization among the sulfate transporters across Saccharomyces species through recent changes in noncoding sequence. Furthermore, these results show a clear example of how such background differences due to paralog divergence can drive changes in genome evolution.

Indexed as

Evolution, MolecularGenetic FitnessAdaptation, PhysiologicalAnion Transport ProteinsGenetic VariationGenome, FungalGenotypeMutationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSelection, GeneticSulfate TransportersAnion Transport ProteinsSaccharomyces cerevisiae ProteinsSUL1 protein, S cerevisiaeSUL2 protein, S cerevisiaeSulfate Transporters

Identifiers

PMID28196070
PMCPMC5308817

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Registered trials

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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.