Evidence map›Paper›PMID 26949252›Full record

ArticleeLife2016

Further support for aneuploidy tolerance in wild yeast and effects of dosage compensation on gene copy-number evolution.

Audrey P Gasch, James Hose, Michael A Newton, Maria Sardi, Mun Yong, Zhishi Wang

Abstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Article
  2. Article
  3. Exploring genome-transcriptome correlations in cancer.Biochemical Society transactions · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A survey of chromosomal instability measures across mechanistic models.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. The reckoning of chromosomal instability: past, present, future.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Practical Approaches for the YeastInternational journal of molecular sciences · 2023
    Review
  18. A survey of CIN measures across mechanistic models.bioRxiv : the preprint server for biology · 2023
    Article
  19. Article
  20. 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

6 authors.

Audrey P GaschLaboratory of Genetics, University of Wisconsin-Madison, Madison, United States.ORCID http://orcid.org/0000-0002-8182-257X
James HoseLaboratory of Genetics, University of Wisconsin-Madison, Madison, United States.
Michael A NewtonGenome Center of Wisconsin, University of Wisconsin-Madison, Madison, United States.
Maria SardiLaboratory of Genetics, University of Wisconsin-Madison, Madison, United States.
Mun YongLaboratory of Genetics, University of Wisconsin-Madison, Madison, United States.
Zhishi WangDepartment of Statistics, University of Wisconsin-Madison, Madison, United States.

Funding

TrainingU54AI117924 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI CRAVEN, MARK W. · 2014 to 2018
$11.3M
Functional Genomics of Stress Defense in YeastR01GM083989 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI GASCH, AUDREY · 2008 to 2016
$3.0M
NIAID NIH HHS U54 AI117924NIAID NIH HHS U54AI117924NIGMS NIH HHS R01 GM083989NIGMS NIH HHS R01GM083989
6 · The paper itself

Abstract

In our prior work by Hose et al., we performed a genome-sequencing survey and reported that aneuploidy was frequently observed in wild strains of S. cerevisiae. We also profiled transcriptome abundance in naturally aneuploid isolates compared to isogenic euploid controls and found that 10-30% of amplified genes, depending on the strain and affected chromosome, show lower-than-expected expression compared to gene copy number. In Hose et al., we argued that this gene group is enriched for genes subject to one or more modes of dosage compensation, where mRNA abundance is decreased in response to higher dosage of that gene. A recent manuscript by Torres et al. refutes our prior work. Here, we provide a response to Torres et al., along with additional analysis and controls to support our original conclusions. We maintain that aneuploidy is well tolerated in the wild strains of S. cerevisiae that we studied and that the group of genes enriched for those subject to dosage compensation show unique evolutionary signatures.

Indexed as

AneuploidyGene DosageGene Expression ProfilingGene Expression Regulation, FungalRNA, MessengerSaccharomyces cerevisiaeRNA, Messengeraneuploidycomputational biologycopy number variationdosage compensationevolutionevolutionary biologygenomics<i>s. cerevisiae</i>systems biology

Identifiers

PMID26949252
PMCPMC4798956

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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.