bioRxiv ScienceSearch

bioRxiv · 10.1101/2021.02.11.430833

The genetic basis of adaptation through the evolution of mating systems

Abstract

Although adaptation can be realized through the fixation of beneficial alleles that increase viability, many plant populations may adapt through the evolution of self-fertilization, especially when pollination becomes inefficient. However, the genetic basis of adaptation through the evolution of selfing remains unclear. Using population genetic models, I study adaptation through the fixation of alleles that increase the selfing rate (selfing modifiers) from new mutations or/and standing variation. For adaptive alleles unrelated to selfing, it is known that selfing promotes adaptation from a new mutation only when the beneficial alleles are recessive, and the probability of adaptation from standing variation is nearly independent of dominance, and always decreases with the selfing rate. In contrast, for adaptation through the evolution of selfing, when it occurs by fixation of a newly arisen mutation, a population that already has a high selfing rate may be more (less) likely to adapt than outcrossers even when the modifier is dominant (recessive) if the modifier is weakly (strongly) selected. Also, adaptation from standing variation is more likely through recessive modifier alleles, with the highest fixation probability found in partially selfing populations, but fixation is fastest when dominance is intermediate. When there are multiple modifiers, adaptation through new mutations is more likely when selfing is controlled by few large-effect rather than many slight-effect modifiers. This study suggests that to understand the genetic basis of adaptation, it is necessary to determine the ecological and genetic advantages of adaptive alleles. Significance statementThis study, by deriving the selective coefficient and effective population size, investigated the genetic basis of adaptation through fixation of modifier alleles that increase the selfing rate, which is shown to differ in several aspects from that through evolution of mating-unrelated alleles. Specifically, when adaptation is from new mutations, the dominance of a selfing modifier allele below which selfing increases the fixation probability depends on the strength of pollen limitation and pollen discounting. Adaptation from standing variation is more likely through recessive modifier alleles and in populations with an intermediate selfing rate. This work suggests it is important to have a mechanistic understanding of how adaptive alleles increase individual fitness in environment that is unfavorable to the population.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Xu, K.. 2021-02-12. The genetic basis of adaptation through the evolution of mating systems. https://doi.org/10.1101/2021.02.11.430833

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Geometry of antigenic evolution improves influenza vaccine selection

Anticipating antigenic evolution is essential for selecting effective seasonal influenza A/H3N2 vaccine strains. To this end, we integrated hemagglutination-inhibition and neutralization titers spanning 2002 to 2025 into a unified Bayesian antigenic map. The map resolves twelve antigenic clusters advancing in discrete steps, with several clusters co-circulating in most seasons. In 15 of 21 seasons, the WHO-recommended vaccine belonged to an earlier cluster than the dominant circulating cluster. The direction of each vaccine update relative to recent viral drift predicted vaccine effectiveness one season ahead in out-of-sample forecasts. Antigenic distance, the conventional measure of vaccine-virus match, was weakly associated with effectiveness until update direction was accounted for. Retrospectively ranking candidate strains by predicted effectiveness would have selected a strain predicted to outperform the WHO recommendation in every season, raising mean predicted effectiveness by 10 percentage points.

evolutionary biology

Evolutionary replay of duplicate-gene retention across independent whole-genome duplications

Whole-genome duplications repeatedly expose ancestral gene lineages to the same broad evolutionary outcome-retention or loss of duplicated copies-but it remains unclear whether this history replays similarly across evolutionary scales. We placed duplicate retention in shared hierarchical orthologous-group coordinates and compared percentile ranks defined within each event-wide mapped universe. Three independent angiosperm whole-genome duplications showed reproducible replay (global rank effect T-replay = 0.210, bootstrap 95% confidence interval 0.172-0.248; permutation P = 1/100,001). A plant reference-panel score specified before target outcomes were examined predicted retention after the Apple/Pear duplication ({rho} = 0.169, n = 373). Deep transfer was heterogeneous: the teleost-genome-duplication estimate was positive but unresolved ({rho} = 0.107, n = 151, 95% confidence interval -0.050 to 0.260), whereas transfer to the ancient budding-yeast whole-genome duplication (yeast WGD) was supported ({rho} = 0.280, n = 186). Independently reconstructed animal outcomes also replayed between teleost and Stylommatophora duplications (r = 0.226, n = 146, P = 0.00326), although the effect remained below a prespecified strong-effect threshold. A strict plant-animal comparison was limited to 25 deeply one-to-one lineages and was unresolved (r = 0.033, 95% confidence interval -0.303 to 0.340). Thus, ancestral gene-lineage identity contributes reproducibly to duplicate retention after independent whole-genome duplications, but replay is structured by evolutionary lineage and modified by event-specific history rather than governed by one universal gene-fate ranking.

evolutionary biology

A Hymenoptera-restricted gene mediating ant castes co-opts deeply conserved machinery to control organ size

Lineage-specific genes are widespread and have been implicated as phenotypic innovation inducers, but how they acquire complex developmental functions remains poorly understood. Ant queens and workers develop dramatically different organ sizes from identical genomes under juvenile hormone (JH) control, yet the molecular effectors translating JH signalling into caste-specific organ growth remain unknown. Here we identify torch, a Hymenoptera-restricted gene, as the most consistently gyne-biased and JH-responsive gene across 68 ant species. Knockdown of torch in virgin queens of Monomorium pharaonis produces a worker-like, multi-organ growth-restricted phenotype. Mechanistically, torch harbours an E-box-like motif activated by the JH receptor Gce-Tai and acts as a GA-repeat-binding transcription factor that regulates Hippo signalling, the deeply conserved organ-size control pathway in animals. Expressing torch heterologously in mice and a growth-restricted Drosophila background shows that the gene retained its general growth-promoting activity across more than 700 million years of animal evolution in lineages that lack the gene, establishing that its function is mediated through conserved rather than ant-specific machinery. A lineage-specific gene can therefore acquire complex morphogenetic function by co-opting ancient organ-size circuitry, providing a general route by which novel genes can drive phenotypic innovation.

evolutionary biology