Aneuploidy Causes Non-genetic Individuality
Open accessAbstract
Phenotypic variability is a hallmark of diseases involving chromosome gains and losses, such as Down syndrome and cancer. Allelic variances have been thought to be the sole cause of this heterogeneity. Here, we systematically examine the consequences of gaining and losing single or multiple chromosomes to show that the aneuploid state causes non-genetic phenotypic variability. Yeast cell populations harboring the same defined aneuploidy exhibit heterogeneity in cell-cycle progression and response to environmental perturbations. Variability increases with degree of aneuploidy and is partly due to gene copy number imbalances, suggesting that subtle changes in gene expression impact the robustness of biological networks and cause alternate behaviors when they occur across many genes. As inbred trisomic mice also exhibit variable phenotypes, we further propose that non-genetic individuality is a universal characteristic of the aneuploid state that may contribute to variability in presentation and treatment responses of diseases caused by aneuploidy.
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The reversibility of aneuploidy offers a dynamic mechanism for fungi to balance adaptation and stability, in the population and for individuals.
“Importantly, its reversibility offers a dynamic mechanism for fungi to balance adaptation and stability, in the population and for individuals [151,155].”
From Insight into the Mechanisms and Clinical Relevance of Antifungal Heteroresistance (2025) · cites this paper as [155]
The Discussion section ‘Aneuploidy decreases robustness of biological networks’ (page not provided) reports variation among individual aneuploid yeast cells and notes that variation in fungal populations can benefit adaptation under stress. The cited paper does not establish that aneuploidy’s reversibility lets fungi balance adaptation with stability, either in populations or in individuals. (LLM, conf=0.83)
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References 61 · Cited by 109
- Authors
- Beach, R. R., Ricci-Tam, C., Brennan, C. M., Moomau, C. A., Hsu, P.-H., Hua, B., Silberman, R. E., Springer, M., & Amon, A.
- Affiliations
- Howard Hughes Medical Institute (US)
- Harvard University (US)
- Corresponding author
- Amon, Angelika
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2017-04
- Volume
- 169
- Issue
- 2
- Pages
- 229-242.e21
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5441241
- OpenAlex
- W2604944651
- Cited by
- 109
- References
- 61
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 11 · 2023: 16 · 2022: 8 · 2021: 9 · 2020: 12 · 2019: 14 · 2018: 16 · 2017: 6
- FWCI
- 7.01
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 370 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (CA206157, GM118066)
- Koch Institute (P30-CA14051)
- National Science Foundation Graduate Research Fellowships
- National Science Foundation (1349248)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- aneuploidy, phenotypic heterogeneity, copy number variation, cell cycle progression, trisomy, Down syndrome, cancer, yeast, treatment response variability
- MeSH terms
- Aneuploidy, Animals, Cell Cycle, Cell Division, DNA Damage, Gene Expression Regulation, Kinetics, Phenotype, Saccharomyces cerevisiae, Genetic Heterogeneity, Mice
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