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<title>bioRxiv Subject Collection: Evolutionary Biology</title>
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This feed contains articles for bioRxiv Subject Collection "Evolutionary Biology"
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<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.26.734751v1?rss=1">
<title>
<![CDATA[
Comparison of directional random walk and weighted least squares modeling of sparse fossil data 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.26.734751v1?rss=1
</link>
<description><![CDATA[
The general random walk model (GRW) of Hunt (2006) is used to infer directional evolution in mean trait values from sparse fossil data by modeling phenotypic change as the accumulated result of small steps with mean step sizes and step variances. Using simulations and real data cases, Ergon (2026) showed that the step variances can be estimated reasonably well only when the mean trait values have small measurement errors, while for fossil data with realistic measurement errors they appear to be extremely difficult to find, and they are often found to be negative. In the simulations Ergon (2026) assumed that the true phenotypic mean values were known. Here, I essentially repeat these simulations under the assumption that only mean trait values with large measurement errors are known, and based on weighted mean squared error (WMSE) comparisons the conclusion is that weighted least squares (WLS) is a better method than GRW. A second conclusion is that WLS is a better method also in the possibly rare cases with large measurement errors where the GRW parameters are estimated well. The GRW method is simply not flexible enough to handle such cases. A third conclusion is that Akaike Information Criterion (AIC) results for GRW models with large measurement errors relative to the step variance may be overly optimistic.
]]></description>
<dc:creator><![CDATA[ Ergon, R. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.26.734751</dc:identifier>
<dc:title><![CDATA[Comparison of directional random walk and weighted least squares modeling of sparse fossil data]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.26.734870v1?rss=1">
<title>
<![CDATA[
From migrants to residents: Genomic insights into adaptive strategies in European robins (Erithacus rubecula) 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.26.734870v1?rss=1
</link>
<description><![CDATA[
Bird migration evolved as an adaptation to seasonally changing habitats. Migratory behaviour can vary within the same species in case of partial migratory behaviour, i.e. one population (or individual) is migratory and another one is resident. Species that exhibit a wide variety of migratory phenotypes provide valuable systems to understand the evolutionary drivers behind different phenotypes and how populations adapt to habitats with distinct seasonality. The European robin (Erithacus rubecula) expresses migratory behaviour in central and northern areas of the species distribution range, whereas populations in the South and on the Macaronesian islands are predominantly resident, providing a suitable system to investigate these questions. We use high coverage whole genome re-sequencing data of 125 European robins to investigate how migration behaviour affects population structure and demography, and how it affects the selection landscape in the genome. Genetic structure in European robins coincides with migratory phenotype and geography and populations are characterised by distinct demographic histories. Our results suggest that both the continental resident population as well as the Macaronesian island populations have derived independently from an ancestral migratory population. Unexpectedly, tests for differential selection revealed extensive positive selection pressure acting across all chromosomes in the resident populations, while selective sweeps are largely absent from migrants. We speculate that this might be an analytical artifact due to mismatching timescales between what population genomics methods can detect and the scale on which migration behaviour likely evolved in the robin. We suggest that future studies on the genomics of migration should more focally account for different time scales on which these processes happen, such as including the wider phylogenomic background of the target species, to capture the full evolutionary history of migratory traits.
]]></description>
<dc:creator><![CDATA[ Langebrake, C., Langebrake, G., Perez-Tris, J., Illera, J. C., Liedvogel, M. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.26.734870</dc:identifier>
<dc:title><![CDATA[From migrants to residents: Genomic insights into adaptive strategies in European robins (Erithacus rubecula)]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.25.734679v1?rss=1">
<title>
<![CDATA[
Nuclear phylogenomics clarifies the family-level backbone and gene-tree conflict in Zingiberales 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.25.734679v1?rss=1
</link>
<description><![CDATA[
Zingiberales includes eight morphologically distinctive families, but its family-level backbone has remained unstable, especially around Musaceae, Heliconiaceae, Lowiaceae, and Strelitziaceae. We analysed 1566 low-copy nuclear genes from 52 samples, representing all eight families and Pontederia crassipes as outgroup. Concatenated maximum likelihood and multispecies coalescent analyses recovered the same backbone: ((Zingiberaceae, Costaceae), (Cannaceae, Marantaceae)) is sister to (Musaceae, (Heliconiaceae, (Lowiaceae, Strelitziaceae))). Penalized-likelihood dating placed the sampled crown group in the Late Cretaceous, with several deep family-level divergences occurring on short internodes. Analysis of 1248 rerooted gene trees showed that conflict is concentrated on these deep branches and in several shallow clades. HyDe tests of empirical and simulated matrices, each including 62,475 triples, did not support widespread ancient hybridization among the major family-level lineages after filtering against the simulated null model. The nuclear data recover a stable Zingiberales backbone, and the long-standing instability of several deep nodes is best explained by rapid early divergence and extensive incomplete lineage sorting.
]]></description>
<dc:creator><![CDATA[ Wang, J., Zhu, Q., Chen, C., Luo, Y., He, J. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.25.734679</dc:identifier>
<dc:title><![CDATA[Nuclear phylogenomics clarifies the family-level backbone and gene-tree conflict in Zingiberales]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.29.735061v1?rss=1">
<title>
<![CDATA[
Evolutionary Origins of Molecular Programs Underlying Brain Circuitry 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.29.735061v1?rss=1
</link>
<description><![CDATA[
The vertebrate pallium harbors independently evolved structures that, nevertheless, support strikingly similar sensory and cognitive circuit architectures. The mechanisms and evolutionary timing driving the emergence of these parallel pallial circuits remain unelucidated. Here, we integrated spatial transcriptomic and single-nucleus RNA-seq datasets from eight representative vertebrate species spanning approximately 500 million years of evolution to reconstruct the evolutionary assembly of the primary sensory-allocortical (Pr-Al) molecular axis, a conserved cortical hierarchical axis defined in our prior work. We uncovered that Pr- and Al-like neuronal identities are deeply conserved across sarcopterygians, encompassing all tetrapods and lobe-finned fishes. Intriguingly, this ancestral neuronal homology is uncoupled from spatially partitioned patterning: only tetrapods further compartmentalized these Pr- and Al- neurons into distinct pallium regions. Functional enrichment of Pr- and Al- gene programs uncovered a conserved tetrapod genetic core suite including MAPK signaling and axon guidance pathways. This core toolkit underwent sequential functional refinement from amphibians through mammals. Notably, mammals and birds convergently evolved association-cortical molecular profiles enriched for synaptic regulatory genes to support advanced cognitive functions. Collectively, this work delineates a stepwise vertebrate pallium evolutionary paradigm that explains how conserved molecular modules shape spatially organized brain circuitry across deep evolutionary time.
]]></description>
<dc:creator><![CDATA[ Huang, Z., Li, S., Zhuang, Z., Chen, D., DU, X., Liu, Q., Du, H., Liu, S., Fan, G., Liu, L., Hao, S., Liu, C., Sun, Y., Ma, S. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.29.735061</dc:identifier>
<dc:title><![CDATA[Evolutionary Origins of Molecular Programs Underlying Brain Circuitry]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.27.734982v1?rss=1">
<title>
<![CDATA[
An adhesion GPCR regulates cell adhesion and mating in the closest living relatives of metazoans 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.27.734982v1?rss=1
</link>
<description><![CDATA[
The transition to metazoan multicellularity required the evolution of cell-surface receptors that coordinate adhesion and signaling under changing environmental conditions. We investigated potential regulators of cell interactions in the choanoflagellate Salpingoeca rosetta, one of the closest living relatives of metazoans. Here, we identify Cupidon, an adhesion G protein-coupled receptor that acts as a dual-function regulator of cell adhesion and mating. Under well-fed (i.e., nutrient-replete) conditions, Cupidon suppresses cell aggregation by inhibiting N-acetylglucosamine-dependent collar-mediated adhesion. Starvation of S. rosetta triggers gametogenesis, resulting in anisogametes: female gametes with an elongated collar and male gametes that form a basal protrusion, the "fertilopod." Cupidon undergoes concurrent changes in proteolytic processing and localization, ultimately concentrating at the gamete contact interface, where it promotes gamete fusion. Together, our findings reveal that aGPCR-mediated regulation of cell adhesion predates the origin of metazoans.
]]></description>
<dc:creator><![CDATA[ Garcia De Las Bayonas, A., Gonzalez, S., King, N. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.27.734982</dc:identifier>
<dc:title><![CDATA[An adhesion GPCR regulates cell adhesion and mating in the closest living relatives of metazoans]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.28.735027v1?rss=1">
<title>
<![CDATA[
In search of intralocus sexual conflict in the multivariate and local genetic architecture of metabolic traits in humans 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.28.735027v1?rss=1
</link>
<description><![CDATA[
Despite a common genome, males and females are remarkably different across species. Intralocus Sexual Conflict (IASC) arises when selection favours different trait values in the sexes but a shared genetic architecture constrains their evolutionary divergence. IASC is typically studied at the single-trait level, and genome-wide architectures can obscure conflict localized to specific genomic regions. We investigated IASC in the multivariate and local genetic architecture of 17 human metabolic traits and lifetime reproductive success by estimating the sex-stratified additive genetic (co)variance matrix (Gmf) and local cross-sex-cross-trait genetic correlations. Genome-wide, between-sex covariance matrix (B) showed only 1.15% asymmetry, and sexually concordant (SC) genetic variation exceeded sexually antagonistic (SA) variation by 18.5-fold. Indirect evolutionary response to SC selection was 1.6-fold stronger than direct responses to SA selection. In contrast, local analyses revealed a more heterogeneous structure - among the regions with significant local correlations, 12% were consistently SA, showing opposite fitness effects in the sexes, with functional enrichment in WNT signalling, while 20% exhibited both SA and SC effects . Our results demonstrate that in human metabolic traits, SC variation predominates genome-wide, whereas SA variation is concentrated in specific local regions, highlighting the importance of integrating multivariate and local frameworks in understanding conflict.
]]></description>
<dc:creator><![CDATA[ Chakraborty, S., Mitra, K., Chakrabarty, A. ]]></dc:creator>
<dc:date>2026-07-01</dc:date>
<dc:identifier>doi:10.64898/2026.06.28.735027</dc:identifier>
<dc:title><![CDATA[In search of intralocus sexual conflict in the multivariate and local genetic architecture of metabolic traits in humans]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-07-01</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.22.733698v1?rss=1">
<title>
<![CDATA[
Diversifications of both the three domains of life and SARS-CoV-2 possibly driven by biases between amino acid biosynthetic families 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.22.733698v1?rss=1
</link>
<description><![CDATA[
All cellular life forms fall under the three-domain classification of life, raising a fundamental evolutionary question: why does this classification feature three rather than two or four? To answer this question, a more general method, rather than the traditional one based on comparing small-subunit ribosomal RNAs, is required. The three-base periodicity in genomes is a common feature of both cellular life forms and viruses, which is species-specifically biased between amino acid biosynthetic families. Based on comparing such a common feature of all life forms, a global triangular diversification picture has been obtained, whose three angular regions correspond to the three domains, respectively. This mechanism of diversification of life attributes the evolutionary driving forces in diversification of the three domains of life to the biases between amino acid biosynthetic families. Notably, the same mechanism also applies to the contemporary diversification of SARS-CoV-2, whose reasonable results in turn corroborate the above explanation of primordial diversification of life and in addition shed light on the mechanism of speciation.
]]></description>
<dc:creator><![CDATA[ Li, D. J. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.22.733698</dc:identifier>
<dc:title><![CDATA[Diversifications of both the three domains of life and SARS-CoV-2 possibly driven by biases between amino acid biosynthetic families]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.25.734618v1?rss=1">
<title>
<![CDATA[
CoalMiner: a coalescent model generator for fastsimcoal2 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.25.734618v1?rss=1
</link>
<description><![CDATA[
Demographic inference using the Site Frequency Spectrum (SFS) is often constrained by the number and complexity of models tested. Here we present a coalescent model generator called CoalMiner for use with fastsimcoal2. CoalMiner utilizes a decision tree framework to generate biologically plausible models, with user input dictating the number and ranges of demographic parameters and histories, which can then be plugged into the fastsimcoal2 pipeline. Using extensive simulations and empirical data, we show that CoalMiner is an effective helper tool to explore demographic model space. CoalMiner is written in Python and is freely available on GitHub: https://github.com/raywray/coalminer with numerous vignettes and tutorials.
]]></description>
<dc:creator><![CDATA[ Esplin-Stout, R., Sethuraman, A. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.25.734618</dc:identifier>
<dc:title><![CDATA[CoalMiner: a coalescent model generator for fastsimcoal2]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.29.735167v1?rss=1">
<title>
<![CDATA[
Indirect genomic effects shape cancer risk across species 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.29.735167v1?rss=1
</link>
<description><![CDATA[
Tumour prevalence varies dramatically throughout the animal kingdom despite broadly conserved cellular and developmental processes, raising the question of how evolution has shaped susceptibility 1,2. Here, we link macroevolutionary variation in tumour prevalence to gene-level selection by integrating comparative genomics data from 109 species of birds and mammals using a Bayesian phylogenetic framework to estimate pangenome-wide rates of genetic evolution across >150 million years of evolutionary change. We identify 3,206 genes in which natural selection is associated with shifts in tumour prevalence, with more than 80% of which are linked to reduced prevalence, suggesting pervasive selection for cancer suppression. Using causal phylogenetic inference, we show that genes associated with reduced tumour prevalence act predominantly through indirect effects on body size, revealing growth as a key mediator of cancer risk across species. In contrast, genes associated with increased tumour prevalence exert direct effects independent of body size. Finally, at the species-level, we demonstrate that exceptionally low rates of benign tumours do not necessarily coincide with reduced malignancy, revealing that benign and malignant tumour processes are evolutionarily decoupled. Together, these results reveal how natural selection has fine-tuned the link between genotype, phenotype, and cancer risk across species.
]]></description>
<dc:creator><![CDATA[ Butler, G., Ramakrishnan, S., Collins, T., Baker, J., Amend, S. R., The Vertebrate Genomes Project Consortium Phase I,, Schatz, M. C., Venditti, C., Pienta, K. J. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.29.735167</dc:identifier>
<dc:title><![CDATA[Indirect genomic effects shape cancer risk across species]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734260v1?rss=1">
<title>
<![CDATA[
Phylogenetic Mosaic of an Arms Race with Asymmetrical Sexual Conflict and Its Macroevolutionary Consequences in a Lineage of Small Water Striders 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734260v1?rss=1
</link>
<description><![CDATA[
Sexual conflict has been hypothesized as a driver of speciation, though its effects are likely heterogeneous across phylogenies and between sexes. The semi-aquatic bug, which inhabits water surfaces across diverse aquatic environments, has long served as a model for studying sexual conflict. While previous studies have focused on rapid antagonistic coevolution and the genetic basis of sexually antagonistic traits, the macroevolutionary consequences of asymmetrical sexual conflict--particularly male-dominated grasping traits versus female resistance--remain largely unexplored. Within the subgenus Pseudovelia, males exhibit pronounced phenotypic diversification in grasping structures, whereas females show modest, clade-specific resistance traits, suggesting male-biased asymmetric conflict. This system presents a valuable opportunity to examine how sexual conflict influences diversification and asymmetrical trait evolution across lineages. Using 204 individuals, representing over half of the subgenus's species diversity, we reconstructed a time-calibrated phylogeny, quantified diversification rates, assessed sexual conflict intensity across clades, and analyzed correlations between sexual trait evolution and diversification. Our results reveal extensive phylogenetic conflict, particularly within the East Asian clade, driven by introgression and incomplete lineage sorting (ILS). Furthermore, we observe significant phylogenetic heterogeneity in both phenotypic evolution and diversification rates. Notably, a male "trait package" enhancing grasping ability likely drives rapid diversification in the recently radiated "South China" lineage. In contrast, grasping traits involving abdominal segment VIII are associated with lower conflict intensity, facilitating greater evolutionary flexibility in female resistance and resulting in lineage-specific counter-adaptations. These findings highlight the heterogeneous dynamics of asymmetrical sexual conflict in shaping diversification and speciation.
]]></description>
<dc:creator><![CDATA[ Li, Z., Chen, H., Jin, Z., Freitag, H., Hecher, C., Zettel, H., Fu, S., Liu, C., Qiao, M., Guo, B., Bu, W., Ye, Z. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734260</dc:identifier>
<dc:title><![CDATA[Phylogenetic Mosaic of an Arms Race with Asymmetrical Sexual Conflict and Its Macroevolutionary Consequences in a Lineage of Small Water Striders]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.733823v1?rss=1">
<title>
<![CDATA[
Phylogenetic correlation between the Type IV Secretion System and HIP1 suggest an adaptation for horizontal gene transfer conserved at the phylum level 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.733823v1?rss=1
</link>
<description><![CDATA[
Most cyanobacterial genomes are rich in the GCGATCGC octamer, also known as Highly Iterated Palindrome 1 (HIP1). Despite its description over three decades ago, the biological function of this highly abundant sequence is only beginning to be elucidated. HIP1 is recognized by two DNA methylases, DmtA and DmtC, and is characterized by its evolutionary conservation and a quasi-periodic distribution within genomes. However, whether the phylogenetic distribution of HIP1 correlates with the presence of functional categories of protein families remains unknown. Here we investigated whether certain protein families share a phylogenetic distribution with this abundant palindromic sequence across cyanobacterial genomes. Our analysis revealed a strong phylogenetic correlation between several proteins of the Type IV secretion system (T4SS) and the abundance of HIP1. This finding aligns with recent discoveries demonstrating that HIP1 enhances DNA transformation in a methylation-dependent manner in two distinct cyanobacterial species. Consequently, we hypothesize that HIP1 function as a conserved adaptation for horizontal gene transfer (HGT) at the phylum level, potentially by serving as a DNA-uptake recognition sequence in cyanobacteria. Keywords: DNA motifs, palindromic DNA sequences, phylogenetic correlation methods, bacterial evolution, horizontal gene transfer. Significance statement. Scientists have long been baffled by the HIP1 sequence, a short, highly common, repetitive DNA pattern found across almost all cyanobacterial genomes. Our study used a whole-genome evolutionary approach and found that the presence of this repetitive pattern is tightly linked to the presence of a cell's external DNA uptake system. This tight co-evolutionary relationship suggests that HIP1 isn't just random genomic feature, but a conserved evolutionary adaptation used by the entire cyanobacterial phylum to specifically enhance their ability to acquire new genes from one another.
]]></description>
<dc:creator><![CDATA[ Rodriguez-Cruz, U., Moreno-Hagelsieb, G., Abreu-Goodger, C., Martinez-Guerrero, C., Delaye, L. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.733823</dc:identifier>
<dc:title><![CDATA[Phylogenetic correlation between the Type IV Secretion System and HIP1 suggest an adaptation for horizontal gene transfer conserved at the phylum level]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734386v1?rss=1">
<title>
<![CDATA[
Gene regulatory divergence underlies tissue-specific and sex-specific misexpression in interspecies nematode hybrids 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734386v1?rss=1
</link>
<description><![CDATA[
Gene regulatory divergence has emerged as a key feature in speciation, influencing gene expression differences that accumulate between diverging populations. Transcriptional regulation, mediated by cis- and trans-acting factors, modulates diverse developmental processes and is responsible for distinct species-specific gene expression profiles. Within interspecies hybrid individuals, negative interactions between divergent cis- and trans-acting factors can lead to gene misregulation and hybrid dysfunction at the organismal level. Such gene regulatory mismatch might disproportionately impact sex-biased and tissue-biased gene regulatory networks due to their unique selective pressures. To address these issues, we investigated the role of regulatory divergence in asymmetric hybrid incompatibility between sister species of Caenorhabditis nematodes (C. remanei, C. latens) by analyzing gene expression of reciprocal hybrids for each sex and key tissue types. Despite severe hybrid male sterility, hybrid males showed less misexpression of sex-biased genes than hybrid females, suggesting that the organismal phenotypic outputs of male-biased gene regulatory networks are more vulnerable to disruption than female-biased genetic networks. Additionally, we found more genes associated with cis- than trans-regulatory divergence, supporting the notion of a disproportionate role for cis-regulatory divergence between species. Moreover, we document extensive cis-trans compensatory X-linked regulatory divergence specifically from male transcriptomes, indicating distinct molecular evolutionary outcomes of stabilizing selection on regulatory controls in males and females. These insights derived from asymmetric hybrid misexpression expand our understanding of the evolution of sex-biased gene regulation in the face of stabilizing selection and identify candidate genes contributing to Caenorhabditis post-zygotic reproductive isolation.
]]></description>
<dc:creator><![CDATA[ Viswanath, A., Fusca, D. D., Calarco, J. A., Cutter, A. D. ]]></dc:creator>
<dc:date>2026-06-30</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734386</dc:identifier>
<dc:title><![CDATA[Gene regulatory divergence underlies tissue-specific and sex-specific misexpression in interspecies nematode hybrids]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-30</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.25.734573v1?rss=1">
<title>
<![CDATA[
Comparative genomics of the unusual arachnid order Solifugae spotlight the molecular and genetic basis for adaptations to arid habitats 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.25.734573v1?rss=1
</link>
<description><![CDATA[
The evolutionary transition to terrestrial life required overcoming several physiological hurdles; however, such challenges were amplified in desert environments. While several xeric-adapted arachnids utilize permanent burrows or "sit-and-wait" foraging strategies as possible energy conservation adaptations in harsh habitats, camel spiders exhibit a counterintuitive, high-energy lifestyle. To investigate the molecular underpinnings distinguishing Solifugae within Chelicerata, we utilized a comparative genomics framework that incorporates a newly sequenced, previously unpublished solifuge genome. We identified lineage-specific expanded orthogroups and evaluated selective pressures acting upon paralogous sequences within our ingroup solifuge species. Additionally, we also focused on fatty acid-associated proteins and heat shock proteins to elucidate how Solifugae may have evolved such anomalous behaviors compared to their arachnid relatives. Our analyses revealed significant signatures of positive selection within key gene families across the solifuge lineage. Notably, paralogs within the cytochrome P450 and biotinidase families showed consistent evidence of selection across all three taxa, suggesting specialized metabolic or detoxification requirements. Furthermore, we identified candidate loci implicated in axonal guidance and lipid metabolism, and a specialized fatty acid enzyme repertoire. While subsequent research is required to determine whether some of the genomic signatures unveiled here are shared across a broader phylogenetic distribution within Solifugae, we establish a critical baseline for future functional validation.
]]></description>
<dc:creator><![CDATA[ Garcia, E. L., Kulkarni, S. S., Graham, M. R., Santibanez-Lopez, C. E., Sharma, P. P. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.25.734573</dc:identifier>
<dc:title><![CDATA[Comparative genomics of the unusual arachnid order Solifugae spotlight the molecular and genetic basis for adaptations to arid habitats]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734300v1?rss=1">
<title>
<![CDATA[
Independent origins of fish endothermy converge on a developmental regulatory signature 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734300v1?rss=1
</link>
<description><![CDATA[
Why independent origins of the same complex physiological trait repeatedly produce similar body forms and physiological changes remains central in evolutionary biology. Endothermy, the internal production and retention of metabolic heat, evolved at least four times in ray-finned fishes, providing natural replicates for convergent genomic signatures. We present a chromosome-scale analysis of three transitions (opah, tunas, and swordfish), including a new chromosome-level genome of the rare, charismatic Pacific oarfish, analyzed with 31 other teleost genomes. The strongest signal is regulatory: of 253,680 conserved noncoding elements, 577 are rate-accelerated in endothermic lineages, with 67 accelerated in all three, exceeding matched ectothermic controls and enriched near developmental transcription factors and Wnt-signaling genes (e.g., irx1a, irx5a, her9, and lmo1). These elements overlap zebrafish developmental enhancers more than expected by chance but are not tied to genes emphasized by expression or coding-selection studies of endothermic lineages, marking a regulatory layer distinct from that metabolic layer. This convergence is part of a broader mosaic: endothermic lineages also share transition-biased substitution and convergent duplication signatures, including excess tandem duplications and lineage-specific gene-family expansion, whereas chromosome organization and protein-coding sequence change little. Endothermic convergence therefore leaves its clearest signal in regulatory remodeling, alongside shifts in substitution bias and gene-family evolution.
]]></description>
<dc:creator><![CDATA[ Arcila, D., Melendez-Vazquez, F., Gallego-Garcia, J., Ignatoff, E., Zhong, J., Pfeiffer, W., Betancur-R., R. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734300</dc:identifier>
<dc:title><![CDATA[Independent origins of fish endothermy converge on a developmental regulatory signature]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734111v1?rss=1">
<title>
<![CDATA[
The contribution of recent and historical demographic histories to genomic diversity and conservation status in plant species 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734111v1?rss=1
</link>
<description><![CDATA[
Demographic factors are intrinsically crucial to evaluate species' extinction risk. However, measuring them remains difficult and time-consuming and the use of genomic summary statistics has been advocated to assess the conservation status of a species. In the present study, we estimated (i) the census number (Nc), (ii) effective population size (Ne) over three different time periods, recent, historical and ancient, (iii) neutral genetic diversity ({pi}4), and (iv) a measure of the efficacy of purifying selection ({pi}0/{pi}4) for 101 plant species using population genomic sequencing data. Twenty-one species are from the Plant Species with Extremely Small Populations (PSESP) program of SW China. Threatened species exhibited significantly lower Ne, Nc, {pi}4, and weaker purifying selection, but had a higher Ne/Nc ratio than non-threatened ones. Nc was the main determinant in identifying conservation status, and contemporary neutral genetic diversity was predominantly influenced by historical Ne. In the absence of demographic information, genetic parameters are a good proxy of conservation status, likely because currently threatened species also had a low historical population size. In summary, our findings suggest that direct estimates of Nc are more useful than {pi}4, although the latter remains a valuable conservation indicator. Hence, efforts such as the PSESP should be extended.
]]></description>
<dc:creator><![CDATA[ Tao, T., Li, P., Zhu, Y., Zhang, S., Zhang, M., Lascoux, M., Chen, J. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734111</dc:identifier>
<dc:title><![CDATA[The contribution of recent and historical demographic histories to genomic diversity and conservation status in plant species]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734261v1?rss=1">
<title>
<![CDATA[
Strategic coexistence theory for evolutionary games 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734261v1?rss=1
</link>
<description><![CDATA[
Evolutionary game theory and ecological coexistence theory both seek to predict the outcome of competition between biological entities, be they strategies or species, but the two fields have relied on largely separate approaches. Replicator equations provide a foundation for analyzing strategy competition, yet they do not explicitly separate the mechanisms that stabilize competition from those that equalize fitness differences between strategies. Here, we extend modern coexistence theory from community ecology to develop strategic coexistence theory (SCT), a framework for quantifying strategic niche and fitness differences between competing strategies. SCT recovers the classic classification of two-strategy games, distinguishing competitive exclusion, coexistence, and priority effects within a shared niche-fitness difference space. Applying SCT to five mechanisms for the evolution of cooperation further reveals that these mechanisms promote cooperation through distinct dynamical routes: kin selection, network reciprocity, and group selection primarily reduce fitness differences, whereas direct and indirect reciprocity destabilize competition and generate priority effects. Finally, applying SCT to microbial public-goods game shows that nonlinear microbial growth can both stabilize and equalize competition between cooperators and defectors, allowing coexistence. Together, these results show that SCT provides a complementary framework for comparing evolutionary games and teasing apart the coexistence mechanisms underlying strategy competition.
]]></description>
<dc:creator><![CDATA[ Park, S. W. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734261</dc:identifier>
<dc:title><![CDATA[Strategic coexistence theory for evolutionary games]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.26.733778v1?rss=1">
<title>
<![CDATA[
The evolution of structural variation across 500 million years of vertebrate evolution 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.26.733778v1?rss=1
</link>
<description><![CDATA[
Structural variants (SVs) contribute substantially to genetic variation and play vital roles in adaptation and disease1,2. Nonetheless, SVs are poorly captured by short reads and thus remain understudied, especially in non-model organisms3,4. Here, using haplotype-resolved genome assemblies from >600 vertebrate species, we comprehensively survey the landscape of SVs across >500 million years of evolution. We identify 35.3 million SVs and 3.12 billion single nucleotide variants (SNVs) segregating between two representative haplotypes across species, with SVs impacting [~]12-fold more base pairs. SV and SNV heterozygosity are correlated across species, with endangered and threatened species exhibiting reduced genetic diversity. However, the contribution of SVs relative to SNVs fundamentally differs across major vertebrate clades: given the same number of SNVs, fishes, amphibians, and reptiles have 4.3-to-9.1 times the number of SVs than birds, and 1.7-to-3.6 times more than mammals. This reduction in the relative contribution of SVs in mammals and birds is linked to fewer non-repeat-associated SVs as well as lower transposable element (TE) abundance and diversity. We identify features underlying genomic instability across vertebrates, finding that SVs frequently occur in repetitive and SNV-rich regions and are mediated by both homology and non-canonical DNA structures. Notably, G-quadruplex structures are enriched 11.5-fold around SV breakpoints in birds, while Z-DNA structures are enriched 2.2-fold in cartilaginous fishes. TEs uniquely contribute to SVs both directly through transposition and indirectly by mediating ectopic recombination, with the proportion of TE-mediated SVs influenced by both genomic TE density and diversity. We identify >10,000 instances of recent TE turnover including extinction of LINE-2 in therian mammals and slowing of CR1 activity in passerine birds. Finally, we show that SVs have an outsized role in functional genetic variation and are >70 times more likely to strongly impact protein-coding sequences than SNVs. While SVs are on average deleterious, we identify extensive recurrent structural variation across multiple taxa in genes involved in sensory, immune, and metabolic systems. Together, this study highlights extraordinary variation in the abundance, composition, mechanism, and functional impact of SVs across vertebrates.
]]></description>
<dc:creator><![CDATA[ Lou, R. N., Lim, D., Daigavane, M., Gozashti, L., Owens, G., Ioannidis, N. M., The Vertebrate Genomes Project Consortium Phase 1,, Sudmant, P. H. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.26.733778</dc:identifier>
<dc:title><![CDATA[The evolution of structural variation across 500 million years of vertebrate evolution]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.28.735080v1?rss=1">
<title>
<![CDATA[
Genomic Distortion of Jawed Vertebrate Phylogeny 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.28.735080v1?rss=1
</link>
<description><![CDATA[
Reconstructing patterns of evolution requires understanding the interrelationships of species, yet evolutionary relationships that defy resolution and calibration in time are commonplace across the Tree of Life. Here, we investigate the dynamics of temporal and topological uncertainty by generating a phylogeny of jawed vertebrates using 1105 exonic loci sampled for 540 species spanning all major orders and most families of gnathostomes. Across loci and DNA sequence sites, we observe rapid reductions in statistical support for the monophyly of jawed vertebrate clades that originated around the Cretaceous-Paleogene mass extinction. Phylogenetic signal was scrambled to different degrees during rapid successive divergences in multiple unrelated jawed vertebrate lineages that radiated in this interval, including birds, snakes, placental mammals, and acanthomorph fishes. In addition to showing that particular events have modified phylogenetic signal across the same loci in distantly related vertebrate clades, we also demonstrate how rates of genomic evolution affect our ability to infer the timescale of vertebrate evolution. By testing how the inclusion of lineages of ray-finned fishes with very fast and slow rates of molecular evolution changes inferences of the vertebrate evolutionary timescale, we show that the deepest divergences in ray-finned fishes may be impossible to accurately infer using sequence data and calibrations from a limited fossil record. These results hint at the macroevolutionary realities underlying topological and divergence time uncertainty across evolutionary trees.
]]></description>
<dc:creator><![CDATA[ Brownstein, C., Yang, L., Dornburg, A., Near, T. J. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.28.735080</dc:identifier>
<dc:title><![CDATA[Genomic Distortion of Jawed Vertebrate Phylogeny]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.25.734355v1?rss=1">
<title>
<![CDATA[
Scalable ARG-free Detection of Denisovan-mediated Superarchaic Introgression Reveals Heterogeneous Patterns across Populations 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.25.734355v1?rss=1
</link>
<description><![CDATA[
Ghost introgression from unsampled hominin lineages has emerged as an increasingly important component of human evolutionary history. Recent studies suggest that deeply divergent hominin lineages may have contributed ancestry either directly to modern humans or indirectly through Denisovan introgression, while inference remains difficult due to few reference genomes, weak signal, and uncertainty in reconstructing deep genealogies. Here we show analytically and through simulations that Denisovan-mediated superarchaic introgression produces predictable shifts in local coalescent depth that can be approximated by scalable summary statistics, particularly pairwise sequence divergence, suggesting that substantial information regarding deeply divergent ancestry is preserved in sequence variations without explicit reconstruction of genealogies. Leveraging this insight, we develop DEEP (Deep ancestry Estimation through Efficient Proxies), an ARG-free neural-network framework for identifying candidate regions of superarchaic ancestry. DEEP retains detectable power at low false positive rates across a broad range of demographic parameter space, remains scalable and recovers signals from small sample sizes. Applying DEEP to Oceanians, Tibetans, and Han Chinese, we identify approximately 0.4-0.6% of genomic windows with evidence of superarchaic ancestry. Candidate regions show both substantial overlap and notable heterogeneity across populations, with repeated enrichment near the HLA locus across all populations, suggesting immune-related regions recurrently retain deeply divergent ancestry.
]]></description>
<dc:creator><![CDATA[ McAllister, N. P., Zoellner, S., Zhang, X. ]]></dc:creator>
<dc:date>2026-06-29</dc:date>
<dc:identifier>doi:10.64898/2026.06.25.734355</dc:identifier>
<dc:title><![CDATA[Scalable ARG-free Detection of Denisovan-mediated Superarchaic Introgression Reveals Heterogeneous Patterns across Populations]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-29</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.23.733933v1?rss=1">
<title>
<![CDATA[
Conservation rescued the Mauritius kestrel from extinction but not from genomic erosion 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.23.733933v1?rss=1
</link>
<description><![CDATA[
Conservation can prevent species extinction via demographic recovery, yet it remains debated whether this translates into genomic recovery and restored fitness. The Mauritius kestrel (Falco punctatus) declined to four known wild birds in 1974 before intensive management recovered the population. Using 130 genomes spanning nearly 200 years, lifetime reproductive success data, and simulations, we reconstructed genomic change across the species collapse and recovery. Long-term small population size had already removed some harmful variation before the crash, a process expected to buffer populations from severe inbreeding depression. Yet the recent bottleneck sharply increased inbreeding, exposed additional harmful variants, and left a signature of genomic erosion associated with reduced reproductive success. The long conservation history of the Mauritius kestrel shows how population collapse and recovery can leave a compounding genetic threat, in which partial genetic purging, continuing genomic erosion, and conservation dependence unfold together in rescued species.
]]></description>
<dc:creator><![CDATA[ Wang, X., Stuart, A., Norris, K., Henshaw, S., Strang, A., Pacheco, C., Nielsen, S. D., Waite, M., Hume, J. P., Ruhomaun, K., Brace, S., Gilbert, M. T. P., Tatayah, V., Jones, C., Groombridge, J., van Oosterhout, C., Morales, H. E. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.23.733933</dc:identifier>
<dc:title><![CDATA[Conservation rescued the Mauritius kestrel from extinction but not from genomic erosion]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.23.733813v1?rss=1">
<title>
<![CDATA[
Minicollagen expression dynamics reveal a transcriptional program for cnidogenesis in the sea anemone Nematostella vectensis 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.23.733813v1?rss=1
</link>
<description><![CDATA[
Cnidae are explosive harpoon-like organelles localized within stinging cells, or cnidocytes, of the phylum Cnidaria (jellyfish, hydroids, sea anemones, and corals). These unique Golgi-derived vesicular structures define the phylum and are prominent examples of an evolutionary cellular novelty. While recent studies have focused on the developmental specification and regulation of cnidocytes more broadly, less is understood about gene expression patterns, structural variations, and toxin repertoires within distinct cnidae subtypes. Here, we determine the transcriptional profile of two major cnidae subtypes in the sea anemone Nematostella vectensis, nematocytes and spirocytes, using the cnidae-specific structural family of proteins called minicollagens. We first define the in vivo expression patterns for three known and three uncharacterized minicollagen orthologs. We show that four minicollagens are broadly expressed throughout ectodermal cnidocytes in developing larvae and primary polyps while two others are restricted to tentacular cnidocytes. Leveraging whole adult scRNA-seq data and two novel transgenic reporter lines, we then demonstrate that the tentacle-restricted cnidocytes are developing spirocytes that are distinguished by expression of the minicollagen NvNcol5. To deepen our analysis of cnidocyte gene expression, we used a customized RNA-FACS-seq pipeline to determine global transcriptional differences between these two subtypes. This approach identified a suite of differentially expressed genes, illuminating spatial and temporal gene expression dynamics across both developing nematocytes and spirocytes. Altogether, our experiments provide fundamental and novel insights into the specialization of cnidarian stinging cells while establishing a rich set of resources for further investigation.
]]></description>
<dc:creator><![CDATA[ Klompen, A. M., Duong, J., McKinney, M. C., Morrison, J. A., Javier, J. E., Chen, S., McKinney, S., Hall, K. E., Petentler, K., Ellington, L., Gibson, M. C. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.23.733813</dc:identifier>
<dc:title><![CDATA[Minicollagen expression dynamics reveal a transcriptional program for cnidogenesis in the sea anemone Nematostella vectensis]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.27.734931v1?rss=1">
<title>
<![CDATA[
Dozens of genetic variants sustain adaptation to urban spatial heterogeneity in Arabidopsis thaliana 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.27.734931v1?rss=1
</link>
<description><![CDATA[
Urbanization creates mosaics of microhabitats that sustain diverse plant communities and offer untapped opportunities to understand contemporary ecological and evolutionary processes. Using a city-wide colonization experiment in Cologne (Germany), we identified the environmental factors limiting establishment and persistence of the ruderal species Arabidopsis thaliana and the genetic variants enabling adaptation. We show that standing genetic variation is essential for realizing the species urban niche, enabling rapid adaptation to fine-scale gradients in disturbance, vegetation, and soil conditions. Despite originating from only two parental genotypes, populations evolved substantial adaptive differentiation within three generations, revealing a highly polygenic basis of local adaptation. More broadly, our approach establishes cities as powerful open-air laboratories for uncovering and fostering ecological and evolutionary processes that generate and sustain biodiversity in human-dominated landscapes.
]]></description>
<dc:creator><![CDATA[ Floret, J., Linstaedter, A., Zhang, H., Hesen, V., Portalier, S., Weinand, L., Bustarret, G., Bell, K., Roux, F., Ali, T., Schmitz, G., Kopriva, S., de Meaux, J. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.27.734931</dc:identifier>
<dc:title><![CDATA[Dozens of genetic variants sustain adaptation to urban spatial heterogeneity in Arabidopsis thaliana]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.22.733620v1?rss=1">
<title>
<![CDATA[
Genomic predictions of climate change vulnerability in the emblematic mountain butterfly Parnassius apollo 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.22.733620v1?rss=1
</link>
<description><![CDATA[
The unprecedented rate of climate warming threatens many species, and assessing their vulnerability to climate change represents a critical challenge in conservation biology. The Apollo butterfly, an emblematic mountain species, is expected to be impacted by climate change. Here, we analysed thousands of SNPs from 101 localities across Apollo French distribution. We identified 93 SNPs strongly associated with climate variation using five genotype-environment association analyses. We forecasted future climate maladaptation of French Apollo populations using four genomic offset methods and integrated these results with neutral and adaptive genetic diversity, genetic structure and adaptive climatic niches to infer their vulnerability to climate change. Jura and Alps populations exhibited the lowest risk of vulnerability to climate change, with low genomic offsets, high genetic diversity and connectivity, whereas Auvergne populations showed the highest genomic offsets and lowest neutral and adaptive genetic diversity. Only a reduced percentage (<1%) of the current distribution is predicted to face climatic conditions outside the current range, suggesting that adaptive variability required to adapt to future climates may already be present, and that assisted gene flow could represent an effective conservation strategy. Finally, we discuss some of the main challenges of genomic forecasts, particularly for declining non-model species.
]]></description>
<dc:creator><![CDATA[ Francisco, T., Lambert-Auger, F., Mazoyer, G., Despres, L. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.22.733620</dc:identifier>
<dc:title><![CDATA[Genomic predictions of climate change vulnerability in the emblematic mountain butterfly Parnassius apollo]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.25.734428v1?rss=1">
<title>
<![CDATA[
Inference of fitness landscapes with heterogeneous patterns of epistasis across sites 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.25.734428v1?rss=1
</link>
<description><![CDATA[
Fitness landscapes provide a framework for understanding how genetic variation shapes evolutionary outcomes. Although these landscapes were long treated as abstract conceptual objects, recent advances in genetic engineering and high-throughput phenotyping have enabled the empirical measurement of phenotypic values across large combinatorial sequence spaces. These developments create a need for statistical frameworks that can summarize, infer, and interpret fitness landscapes in the presence of complex genetic interactions. Here, we introduce a framework for summarizing the structure of genetic interactions across sites based on the average squared local k-way epistatic coefficients between mutations at different subsets of sites, and derive the precise manner in which the variance in these local k-way epistatic coefficients across backgrounds relates to epistasis of orders higher than k. These statistics can be computed exactly for complete combinatorial landscapes and are related to classical statistics in the fitness landscape literature. Moreover, they can be estimated from empirical correlations when data are incomplete or noisy, and used to define an empirical Bayes prior for fitness landscape inference that differentially penalizes interactions involving different subsets of sites. We apply this inference method to diverse high-throughput protein and RNA combinatorial mutagenesis datasets and find that fitness landscapes often show highly structured patterns of genetic interactions across positions. Finally, we use this model to infer a fitness landscape for a dynamic self-splicing intron comprising 65,536 genotypes, and describe in detail the main genetic interactions that shape the structure of this landscape and how they relate to the underlying molecular mechanism. Together, these results provide new tools for summarizing and modeling complex fitness landscapes, and for linking large-scale empirical data to the mathematical theory of fitness landscapes.
]]></description>
<dc:creator><![CDATA[ Marti-Gomez, C., McCandlish, D. M. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.25.734428</dc:identifier>
<dc:title><![CDATA[Inference of fitness landscapes with heterogeneous patterns of epistasis across sites]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.23.733212v1?rss=1">
<title>
<![CDATA[
The genomic origins and evolutionary path to a key innovation in the world's most venomous snakes 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.23.733212v1?rss=1
</link>
<description><![CDATA[
Evolutionary innovation is a key driver of the colonization of new environments and the adaptive radiations of major groups. Novel traits typically evolve through the modification of pre-existing characters but the genetic paths underlying their origin have been challenging to trace, and the general requirements for and relative order of different kinds of gene mutations have been difficult to assess. Here, we trace the genomic origins of four procoagulant venom toxins (factor X, factor V, group I phospholipase A2, and Kunitz-type toxins) that collectively underlie a novel, especially potent blood-clotting venom type in the recently evolved Australian brown snake and taipan clade. We discover evidence for a previously unknown fifth toxin, coagulation factor VII, and show that the toxins evolved through two distinct genetic paths. The factor X and factor V toxins evolved through the sequential de novo co-option of ancestral clotting factor proteins that entailed their heterotopic expression in the venom gland, the fixation of segmental duplications containing each locus, and subsequent gain-of-function mutations that rendered factor X and factor V constitutively active. In contrast, the phospholipase A2 and Kunitz-type toxins evolved by modifying the functions of neurotoxins that were part of the venom arsenal. Our findings support models in which innovative mutations in single-copy genes precede gene duplication in the evolution of novel proteins and offer a rare view into the genesis of a complex trait that has played a central role in a major adaptive radiation.

Significance StatementThis study investigates how an entirely new blood-clotting venom type evolved during the recent radiation of Australias iconic venomous snakes. We traced the key genetic events that occurred on the evolutionary path to one of the worlds most potent venoms. We found that the novel venom activity evolved through the sequential co-option of multiple proteins of the snakes own blood-clotting system, followed by the modification of two venom neurotoxins into proteins with procoagulant activities. We suggest that these unique de novo gene co-options are seminal events that can unlock new ecological strategies, which in turn, may enable major adaptive radiations.
]]></description>
<dc:creator><![CDATA[ van Thiel, J., Dowell, N., Smith, C. F., Sanchez, E. E., Carroll, S. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.23.733212</dc:identifier>
<dc:title><![CDATA[The genomic origins and evolutionary path to a key innovation in the world's most venomous snakes]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.23.734044v1?rss=1">
<title>
<![CDATA[
Sociality changes Gene Essentiality 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.23.734044v1?rss=1
</link>
<description><![CDATA[
Transposon insertion sequencing (Tn-seq) has become a powerful tool for assigning gene fitness and essentiality in bacteria, and has recently been extended to bacteriophages. A core but rarely examined assumption of these screens is that fitness is measured in an asocial environment, where each mutant succeeds or fails on its own. Yet many genes act socially: their products can be shared among neighbors, allowing defective mutants to be complemented in trans. In phages multiple genotypes routinely coinfect the same cell. Here we show that social interactions distort gene essentiality. Using paired quorum-sensing microarray and Tn-seq data from Pseudomonas aeruginosa, we find that quorum-sensing-regulated genes are over-represented among genes scored as non-essential, confirming that social genes are under-reported as essential. We then build a stochastic, agent-based model of phage Tn-seq across an MOI gradient, assigning each gene an intrinsic fitness effect and a complementation fraction. Complementable ("social") genes rise in frequency as MOI increases, masking their true fitness cost, whereas non-complementable ("private") genes, do not. Partitioning genes by life-cycle stage and applying a two-round high-then-low-MOI design, further separates gene functions by life cycle stage. We argue that deliberate MOI manipulation turns a confound into a tool, enabling systematic classification of phage sociality.
]]></description>
<dc:creator><![CDATA[ Smith, E., Humphrey, A., Gurney, J. ]]></dc:creator>
<dc:date>2026-06-28</dc:date>
<dc:identifier>doi:10.64898/2026.06.23.734044</dc:identifier>
<dc:title><![CDATA[Sociality changes Gene Essentiality]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-28</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.26.734749v1?rss=1">
<title>
<![CDATA[
Bacteriophage Heteroresistance as a Cause of Treatment Failure in Urinary Tract Infections 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.26.734749v1?rss=1
</link>
<description><![CDATA[
With the rise of antimicrobial resistance, urinary tract infections (UTIs) have become increasingly more difficult to treat, prompting renewed interest in bacteriophage (phage) therapy as an alternative or adjunct to antibiotics. UTIs are an attractive target for phage therapy because they generate a high density of actively replicating bacteria that supports phage propagation, and because the urinary tract is readily accessible for administration and monitoring. Yet studies of phage therapy for UTIs report mixed outcomes, including failures to meet clinical and microbiological endpoints.

Here we follow the population dynamics of a clinical Escherichia coli UTI strain and two phages, HP3 and ES19, to which the strain appears susceptible by standard testing. Despite this apparent susceptibilty, both phages fail to suppress the strain, with resistance emerging almost immediately. Using the measured mutation rate, our mathematical model shows that traditional resistance cannot account for these dynamics. We instead demonstrate, including by a phage-specific population analysis profile assay we developed, that heteroresistance drives this rapid failure, offering a plausible explanation for treatment failures in UTI phage therapy.
]]></description>
<dc:creator><![CDATA[ Singh-Ward, S., Ismail, A. S., Gil-Gil, T., Berryhill, B. A., Woodworth, M. H., Shanks, H. E., Levin, B. R. ]]></dc:creator>
<dc:date>2026-06-27</dc:date>
<dc:identifier>doi:10.64898/2026.06.26.734749</dc:identifier>
<dc:title><![CDATA[Bacteriophage Heteroresistance as a Cause of Treatment Failure in Urinary Tract Infections]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-27</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.26.734461v1?rss=1">
<title>
<![CDATA[
Comparing genomic inbreeding of an isolated rhesus macaque study population to wild populations 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.26.734461v1?rss=1
</link>
<description><![CDATA[
Long-term studies of isolated animal populations have greatly improved the understanding of various evolutionary processes. However, potentially elevated inbreeding in those compared to wild populations is a common concern. Conventionally, inbreeding has been investigated using reconstructed pedigrees, but nowadays it can be done directly at the genomic level. Here, we utilize genomic data from an intensively studied isolated rhesus macaque (Macaca mulatta) population on the small island Cayo Santiago (Puerto Rico), which was founded in 1938 with wild animals from India. We quantified inbreeding levels by inferring runs of homozygosity (ROH), i.e., long identical haplotypes inherited from both parents. We identified ROH in 97 [~]5x-coverage genomes from Cayo Santiago and, for comparison, in 79 rhesus macaque genomes from five wild populations from China. Notably, this conventionally considered low-coverage data proved sufficient to infer ROHs >4 centimorgans long after imputing the genomes using a reference panel. Our results revealed that the ROH-derived effective population size on Cayo Santiago, 420 individuals, falls within the ranges we inferred in wild populations. Moreover, a general scarcity of individuals with long ROH in both the Cayo and wild populations indicates very few cases of close-kin breeding, suggesting that mechanisms to avoid close-kin breeding operate in rhesus macaques, both in wild and isolated populations. Taken together, our results suggest that Cayo Santiago remains a representative study population.
]]></description>
<dc:creator><![CDATA[ Pautet, F., Freudiger, A., Ruiz-Lambides, A., Widdig, A., Ringbauer, H. ]]></dc:creator>
<dc:date>2026-06-27</dc:date>
<dc:identifier>doi:10.64898/2026.06.26.734461</dc:identifier>
<dc:title><![CDATA[Comparing genomic inbreeding of an isolated rhesus macaque study population to wild populations]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-27</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.24.734279v1?rss=1">
<title>
<![CDATA[
Maintenance of viral diversity through influenza transmission bottlenecks: a within-host branching-process model 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.24.734279v1?rss=1
</link>
<description><![CDATA[
Viral populations can experience a dramatic reduction in population size and genetic diversity during transmission between donor and recipient hosts. Transmission bottlenecks can therefore decrease the evolutionary potential of viral populations, slowing adaptation by increasing the strength of genetic drift and decreasing the strength of selection. Recent barcoded influenza experiments in guinea pigs showed that recipient animals receive a diverse viral inoculum but lose most of that diversity within one to two days. The resulting bottleneck therefore arises not at physical transfer but during early viral growth in the recipient. We develop a branching-process framework to quantify how much of this loss follows from stochasticity in early growth alone. Each transmitted lineage is treated as an independent stochastic process governed by measurable viral parameters. We recover these parameters from viral growth rates estimated from observed viral load. A residual filter for each animal then captures any additional loss imposed by the recipient host. Applied to twenty-four recipient animals, the model reveals two distinct groups. For roughly half of the animals, the stochastic extinction during early growth already accounts for the observed loss. For the remaining animals, the additional host filter is severe. Only about one in a hundred free virions pass through. This decomposition offers a quantitative entry point for future work on immune contributions to transmission bottlenecks.
]]></description>
<dc:creator><![CDATA[ Zhang, W., Ellingson, L., Bono, L. ]]></dc:creator>
<dc:date>2026-06-27</dc:date>
<dc:identifier>doi:10.64898/2026.06.24.734279</dc:identifier>
<dc:title><![CDATA[Maintenance of viral diversity through influenza transmission bottlenecks: a within-host branching-process model]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-27</prism:publicationDate>
<prism:section></prism:section>
</item>
<item rdf:about="https://www.biorxiv.org/content/10.64898/2026.06.27.734823v1?rss=1">
<title>
<![CDATA[
Pax6-dependent patterning in an annelid informs the evolution of bilaterian nerve cords 
]]>
</title>
<link>
https://www.biorxiv.org/content/10.64898/2026.06.27.734823v1?rss=1
</link>
<description><![CDATA[
Conserved dorsoventral patterning systems have been proposed as evidence for a common evolutionary origin of centralized nervous systems in Bilateria, yet functional evidence outside vertebrates and arthropods remains limited. Here, we investigated the role of pax6 in the annelid Platynereis dumerilii using a mutant carrying a 61 bp deletion in the paired-domain coding region. Loss of pax6 disrupted ventral neuroectodermal patterning at 34 hpf, causing a shift in nk2.2 expression, narrowing of the nk6 domain, and downregulation of pax3/7, while msx expression remained largely unaffected. These early patterning defects were followed by selective neuronal abnormalities at 48 hpf, including displacement of TrpH-positive serotonergic cells and loss of posterior hb9-positive motoneuron domains. By 6 dpf, additional defects were observed in TrpH, ChAT, VAChT, and nk2.2 expression, accompanied by severe disruption of ventral nerve cord morphology and loss of the characteristic rope-ladder architecture. Together, these findings identify pax6 as a key regulator linking dorsoventral progenitor patterning, neuronal subtype specification, and nervous system morphogenesis in Platynereis. Our results provide functional evidence that the conserved dorsoventral patterning network plays an essential role in annelid ventral nerve cord development and support the view that important components of bilaterian nervous system patterning predate the divergence of major animal lineages.
]]></description>
<dc:creator><![CDATA[ Doderovic, J., Kolek, M., Zitova, A., Kozmikova, I., Kozmik, Z. ]]></dc:creator>
<dc:date>2026-06-27</dc:date>
<dc:identifier>doi:10.64898/2026.06.27.734823</dc:identifier>
<dc:title><![CDATA[Pax6-dependent patterning in an annelid informs the evolution of bilaterian nerve cords]]></dc:title>
<dc:publisher>Cold Spring Harbor Laboratory</dc:publisher>
<prism:publicationDate>2026-06-27</prism:publicationDate>
<prism:section></prism:section>
</item>
</rdf:RDF>
