| Literature DB >> 28388408 |
Rebecca R Beach1, Chiara Ricci-Tam2, Christopher M Brennan1, Christine A Moomau1, Pei-Hsin Hsu1, Bo Hua2, Rebecca E Silberman1, Michael Springer2, Angelika Amon3.
Abstract
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.Entities:
Keywords: Down syndrome; aneuploidy; biological noise; cancer; cell-to-cell variability; gene dosage effects; non-genetic heterogeneity
Mesh:
Year: 2017 PMID: 28388408 PMCID: PMC5441241 DOI: 10.1016/j.cell.2017.03.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582