Many organisms live in predictable environments with periodic variation in growth condition. Adaptation to these conditions can lead to loss of nonessential functions, which could be maladaptive in new environments. Alternatively, living in a predictable environment can allow populations to accumulate cryptic genetic variation that may have no fitness benefit in that condition, but can facilitate adaptation to new environments. However, how these processes together shape fitness of populations growing in predictable environments remains unclear. Through laboratory evolution experiments in yeast, we show that populations grown in a nutrient-rich environment for 1000 generations generally have reduced fitness and lower adaptability to novel stressful environments. These populations showed metabolic remodeling and increased lipid accumulation in rich medium which seemed to provide osmotic protection in salt stress. Subsequent adaptation to stressors was primarily driven by de novo mutations, with very little contribution from the mutations accumulated prior to the exposure. Thus, our work suggests that without exposure to new environments, populations might lose their ability to respond effectively to these environments. Further, our findings highlight a major role of exaptation and de novo mutations in adaptation to new environments, but do not reveal a significant contribution of cryptic variation in this process.
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Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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Site | Modification | Modifier | Source | Reference |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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