Beyond Fixation: Persistent Genetic Variation Under Intense Selection
Arnold, K. R.; Greenspan, Z. S.; Robinson, R. D.; Pupo, A.; Chavarin, V. V.; Chang, K. S.; Cannell, C. O.; Qi, M.; Mueller, L. D.; Rose, M. R.; Phillips, M. A.
Show abstract
Understanding how and why genetic variation is maintained under sustained selection remains a central question in evolutionary genetics. Experimental evolution shows that adaptation in sexually reproducing populations is often highly polygenic, proceeding through coordinated, genome-wide allele frequency shifts from standing variation rather than classic hard sweeps. Recent explanations emphasize highly polygenic architectures, optimizing-selection, and genetic redundancy, which can slow fixation by distributing selection across many loci during adaptation. However, observations from long-term selection experiments reveal a pattern these frameworks do not fully explain: substantial genetic variation persists after hundreds of generations of intense directional selection in constant environments. Here, we use long-term experimental evolution in Drosophila melanogaster to test whether balancing-selection actively maintains genetic variation under strong life-history selection and preserves evolutionary reversibility. Longstanding populations selected for accelerated or delayed reproduction were shifted to the opposing regime, imposing age-structured fitness trade-offs. Notably, selection for early reproduction is associated with substantial loss of genetic variation, providing a stringent test of whether standing variation is truly depleted. Following reciprocal shifts, populations showed rapid phenotypic convergence toward the target regime. At the genomic level, allele-frequency trajectories were strongly antiparallel and highly repeatable across replicates, revealing coordinated polygenic responses. Relaxing long-standing early-life selection produced a pronounced rebound in genome-wide heterozygosity. Deep sequencing uncovered ultra-rare alleles at sites appearing fixed under standard coverage, indicating low-frequency functional variation persists below detection thresholds. These results suggest that substantial genetic variation can persist under intense directional selection and be rapidly redeployed when selection reverses, consistent with widespread balancing-selection.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- The genomic architecture of adaptation to larval malnutrition points to a trade-off with adult starvation resistance in Drosophila 97%
- Maintenance of adaptive dynamics and no detectable load in a range-edge out-crossing plant population 97%
- Evolutionary Insights from a Large-scale Survey of Population-genomic Variation 96%
Similar papers in this journal
Similar papers in this journal
- Distinct patterns of genetic variation at low-recombining genomic regions represent haplotype structure 97%
- Clinal and seasonal change are correlated in Drosophila melanogaster natural populations 96%
- Sexually discordant selection is associated with trait specific morphological changes and a complex genomic response 96%
Similar papers in this journal
Similar papers in this journal
- Genomic time-series data show that gene flow maintains high genetic diversity despite substantial genetic drift in a butterfly species 96%
- Low concordance of short-term and long-term selection responses in experimental Drosophila populations 96%
- Faster-haplodiploid evolution under divergence-with-gene-flow: simulations and empirical data from pine-feeding hymenopterans 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.