Evidence map›Paper›PMID 39584496›Full record

ArticleGenetics2025

On the rate of aneuploidy reversion in a wild yeast model.

James Hose, Qi Zheng, Nathaniel P Sharp, Audrey P Gasch

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

James HoseCenter for Genomic Science Innovation, University of Wisconsin-Madison, Madison, WI 53706, USA.
Qi ZhengSchool of Public Health, Texas A&M University, College Station, TX 77843, USA.
Nathaniel P SharpLaboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0001-6016-083X
Audrey P GaschCenter for Genomic Science Innovation, University of Wisconsin-Madison, Madison, WI 53706, USA.ORCID 0000-0002-8182-257X

Funding

Dissecting the influence of genetic background on aneuploidy tolerance in the model eukaryote Saccharomyces cerevisiaeR01GM147271 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI GASCH, AUDREY · 2022 to 2025
$1.2M
Understanding how aneuploidy disrupts quiescence in the model eukaryote Saccharomyces cerevisiaeR01GM148975 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Audrey Gasch · 2023 to 2026
$1.2M
The evolutionary and genomic drivers of mutation spectraR35GM154954 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Nathaniel Sharp · 2024 to 2026
$1.1M
APGNIGMS NIH HHS R01 GM147271NIGMS NIH HHS R01 GM148975NIGMS NIH HHS R35 GM154954NIHR01GM147271
6 · The paper itself

Abstract

Aneuploidy, arising from the gain or loss of chromosomes due to nondisjunction, is a special class of mutation. It can create significant phenotypic changes by altering the abundance of hundreds of genes in a single event, providing material for adaptive evolution. But it can also incur large fitness costs relative to other types of mutations. Understanding the mutational dynamics of aneuploidy is important for modeling its impact in nature, but aneuploidy rates are difficult to measure accurately. One challenge is that aneuploid karyotypes may revert back to euploidy, biasing forward mutation rate estimates-yet the rate of aneuploidy reversion is largely uncharacterized. Furthermore, current rate estimates are confounded because fitness differences between euploids and aneuploids are typically not accounted for in rate calculations. We developed a unique fluctuation assay in a wild-yeast model to measure the rate of extra-chromosome loss across 3 aneuploid chromosomes while accounting for fitness differences between aneuploid and euploid cells. We show that incorporating fitness effects is essential to obtain accurate estimates of aneuploidy rates. Furthermore, the rate of extra-chromosome loss, separate from karyotype fitness differences, varies across chromosomes. We also measured rates in a strain lacking RNA-binding protein Ssd1, important for aneuploidy tolerance and implicated in chromosome segregation. We found no role for Ssd1 in the loss of native aneuploid chromosomes, although it did impact an engineered chromosome XV with a perturbed centromeric sequence. We discuss the impacts and challenges of modeling aneuploidy dynamics in real-world situations.

Indexed as

AneuploidyModels, GeneticSaccharomyces cerevisiaeChromosome SegregationChromosomes, FungalGenetic FitnessSaccharomyces cerevisiae ProteinsSaccharomyces cerevisiae Proteinsaneuploidychromosome nondisjunction ratemutation accumulation

Identifiers

PMID39584496
PMCPMC13031112

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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.