Search bioRxivSearch

bioRxiv · 10.1101/2020.01.11.902759

Genome-Wide Search for Candidate Drivers of Adaptation Reveals Genes Enriched for Shifts in Purifying Selection (SPurS)

Abstract

An open question in comparative evolutionary genomics is whether or not certain loci are the primary drivers of divergence between taxonomic lineages or species groups. Alternatively, genetic drivers of species divergence may be evenly distributed across the genome. The increasing availability of genome sequences from diverse taxa has enabled the development of novel methods to address this question. Genomes of many highly diverged species may now be compared in order to tease apart genetic differences that drive adaptive or functional divergence, and genetic differences that are observed by chance and are not causally linked to traits that differ between species or lineages. In order to test the hypothesis that a particular subset of loci or genes is responsible for driving adaptive changes between mammals and non-mammals, we developed a novel comparative approach to identify sites that are highly conserved within lineages or species groups and diverge between them. Loci with a high concentration of these sites may be called Shifts in Purifying Selection (SPurS) because a change has occurred between two groups of species at some point in the past, and the shift is conserved (via purifying selection) over a long period of time. Evaluating 7484 orthologous gene copies from 76 vertebrate species, we developed an empirical distribution of SPurS across the genome between Synapsida (placental and non-placental mammals) and Sauropsida (birds, crocodilians, squamates, and turtles), and compared this distribution to the expected null distribution of SPurS using matched simulated data. We then identified a subset of genes that is enriched for SPurS, relative to the full set of genes and to their matched simulated alignments. These SPurS-enriched genes are thus likely candidate drivers of functional divergence or adaptation between the mammalian and non-mammalian species groups in our analysis. Investigators seeking to identify genetic drivers of inter-species evolution may find this method useful, and we provide a web-based software interface to facilitate its use.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Popejoy, A. B., Domanska, D., Thomas, J. H.. 2020-01-13. Genome-Wide Search for Candidate Drivers of Adaptation Reveals Genes Enriched for Shifts in Purifying Selection (SPurS). https://doi.org/10.1101/2020.01.11.902759

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