bioRxiv ScienceSearch

bioRxiv · 10.1101/115089

POUMM: An R-package for Bayesian Inference of Phylogenetic Heritability

Abstract

AO_SCPLOWBSTRACTC_SCPLOWPhylogenetic comparative methods have been used to model trait evolution, to test selection versus neutral hypotheses, to estimate optimal trait-values, and to quantify the rate of adaptation towards these optima. Several authors have proposed algorithms calculating the likelihood for trait evolution models, such as the Ornstein-Uhlenbeck (OU) process, in time proportional to the number of tips in the tree. Combined with gradient-based optimization, these algorithms enable maximum likelihood (ML) inference within seconds, even for trees exceeding 10,000 tips. Despite its useful statistical properties, ML has been criticised for being a point estimator prone to getting stuck in local optima. As an elegant alternative, Bayesian inference explores the entire information in the data and compares it to prior knowledge but, usually, runs in much longer time, even for small trees. Here, we propose an approach to use the full potential of ML and Bayesian inference, while keeping the runtime within minutes. Our approach combines (i) a new algorithm for parallel likelihood calculation; (ii) a previously published method for adaptive Metropolis sampling. In principle, the strategy of (i) and (ii) can be applied to any likelihood calculation on a tree which proceeds in a pruning-like fashion leading to enormous speed improvements. As a showcase, we implement the phylogenetic Ornstein-Uhlenbeck mixed model (POUMM) in the form of an easy-to-use and highly configurable R-package. In addition to the above-mentioned usage of comparative methods, the POUMM allows to estimate non-heritable variance and phylogenetic heritability. Using simulations and empirical data from 487 mammal species, we show that the POUMM is far more reliable in terms of unbiased estimates and false positive rate for stabilizing selection, compared to its alternative - the non-mixed Ornstein-Uhlenbeck model, which assumes a fully heritable and perfectly measurable trait. Further, our analysis reveals that the phylogenetic mixed model (PMM), which assumes neutral evolution (Brownian motion) can be a very unstable estimator of phylogenetic heritability, even if the Brownian motion assumption is only weakly violated. Our results prove the need for a simultaneous account for selection and non-heritable variance in phylogenetic evolutionary models and challenge stabilizing selection hypotheses stated in numerous macro-evolutionary studies.

Explore related subjects

Keep this discovery

BibTeXRIS

Mitov, V., Stadler, T.. 2017-03-08. POUMM: An R-package for Bayesian Inference of Phylogenetic Heritability. https://doi.org/10.1101/115089

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