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. 2017 May 17;83(11):e03206-16. doi: 10.1128/AEM.03206-16

TABLE 1.

Examples of whole-chromosome copy number variations acquired during laboratory evolution experiments with Saccharomyces cerevisiae strainsa

Selected phenotype Aneuploid chromosome(s) Confirmed causality Contributing gene(s) Reference
Biomass sedimentation Whole-genome duplication Yes ACE2 105
Glucose-limited growth Whole-genome duplication Yes 107
High temp tolerance III (+1) Yes 17 individual genes 103
High pH tolerance V (+1) Yes 103
Glucose-limited growth I (+1), III (+1), V (+1) No 108
Phosphate-limited growth IV (+1), VI (+1), X (+1), XIII (+2), XVI (+1) No 108
Lactate utilization by jen1Δ strain III (+1) Yes ADY2 112
Xylose utilization I (−1) No 160
p-Coumaric and ferulic acid tolerance XIV (+1) No 160
Copper tolerance II (+1), VIII (+1) No CUP1, SCO1, and SCO2 104
Galactose tolerance VIII (+1) Yes GAL80 161
Ethanol tolerance III (+1), VIII (+1) No 106
Radicicol resistance XV (+1) Yes STI1 and PDR5 113
Fluconazole resistance VIII (+1) No ERG11 113
Tunicamycin resistance XVI (−1) Yes 113
Benomyl resistance XII (−1) No 113
Suppressors of MEC1 deficiency IV (+1) Yes RNR1 162
Suppressors of MYO1 deletion XIII (+1), XVI (+1) Yes HSP82, HSC82, RLM1, and MKK2 94
Suppressors of RPS24A and RNR1 deletion IX (+1) No RPS24B and RNR3 163
Suppressors of telomerase insufficiency VIII (−1) No PRP8, UTP9, KOG1, and SCH9 164
a

In the examples listed, the acquired CCNV was hypothesized to contribute to the selected phenotype. “Confirmed causality” indicates that a causal link between CCNV and the phenotype acquired during laboratory evolution was experimentally confirmed. In cases where the impact of a CCNV on phenotype was linked to specific genes, this is also indicated. Segmental aneuploidies observed in the cited studies are not included in the table.