<?xml version='1.0' encoding='UTF-8'?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:webfeeds="http://webfeeds.org/rss/1.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:content="http://purl.org/rss/1.0/modules/content/" version="2.0">
  <channel>
    <title>eLife: latest articles by subject</title>
    <link>https://elifesciences.org</link>
    <description>Articles published by eLife, filtered by given subjects</description>
    <atom:link href="https://observer.elifesciences.org/report/latest-articles-by-subject" rel="self"/>
    <docs>http://www.rssboard.org/rss-specification</docs>
    <generator>observer (using python-feedgen)</generator>
    <language>en</language>
    <lastBuildDate>Fri, 09 Oct 2026 14:32:14 +0000</lastBuildDate>
    <webfeeds:analytics id="G-TZ0BM7CV5E" engine="GoogleAnalytics"/>
    <item>
      <title>Intersecting experimental evolution and CRISPR screens to identify novel toxin resistance loci</title>
      <link>https://elifesciences.org/articles/111773</link>
      <description>Understanding toxin resistance in insects is key to appreciating niche adaptations but remains challenging due to its often-polygenic basis. A well-known example is the specialized association of &lt;i&gt;Drosophila sechellia&lt;/i&gt; with noni fruit (&lt;i&gt;Morinda citrifolia&lt;/i&gt;), which is toxic to other insects, including &lt;i&gt;Drosophila simulans&lt;/i&gt; and &lt;i&gt;Drosophila melanogaster&lt;/i&gt;. The main noni toxin is octanoic acid (OA), but the mechanisms that determine sensitivity or resistance to OA in different species remain unclear. Here, we experimentally evolved &lt;i&gt;D. simulans&lt;/i&gt; with increased OA resistance, identifying multiple loci under selection. Cross-referencing these with a genome-wide, OA resistance CRISPR screen in a &lt;i&gt;D. melanogaster&lt;/i&gt; cell line highlighted two proteins: Kraken, a putative detoxification enzyme expressed in digestive and renal tissues, and Alkbh7, a mitochondrial protein linked to fatty acid metabolism. Both genes show elevated expression in &lt;i&gt;D. sechellia&lt;/i&gt; and OA-resistant &lt;i&gt;D. simulans&lt;/i&gt;. In &lt;i&gt;D. melanogaster&lt;/i&gt;, &lt;i&gt;kraken&lt;/i&gt; mutants are more OA-sensitive, while &lt;i&gt;Alkbh7&lt;/i&gt; overexpression increased OA resistance. Mutation of these genes in &lt;i&gt;D. sechellia&lt;/i&gt; reduced OA tolerance. Our identification of genes contributing to OA resistance in laboratory and natural contexts demonstrates how complementary selection approaches can provide insights into complex mechanisms of toxin susceptibility and adaptation. Such methods could have practical applications in the characterization of natural and artificial insecticides.</description>
      <author>Richard.Benton@unil.ch (Camilla Roselli)</author>
      <author>Richard.Benton@unil.ch (Dafni Hadjieconomou)</author>
      <author>Richard.Benton@unil.ch (Joydeep De)</author>
      <author>Richard.Benton@unil.ch (Matthew Butnaru)</author>
      <author>Richard.Benton@unil.ch (Michele Marconcini)</author>
      <author>Richard.Benton@unil.ch (Norbert Perrimon)</author>
      <author>Richard.Benton@unil.ch (Raghuvir Viswanatha)</author>
      <author>Richard.Benton@unil.ch (Richard Benton)</author>
      <author>Richard.Benton@unil.ch (Srishti Goswami)</author>
      <author>Richard.Benton@unil.ch (Steeve Cruchet)</author>
      <author>Richard.Benton@unil.ch (Stephanie E Mohr)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.111773</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Fri, 11 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Pre-Cambrian origin of &lt;i&gt;envelope&lt;/i&gt;-carrying retrotransposons in metazoans</title>
      <link>https://elifesciences.org/articles/108449</link>
      <description>Retrotransposons or endogenous retroviruses (ERVs) essentially carry open reading frames of &lt;i&gt;gag&lt;/i&gt; and &lt;i&gt;pol&lt;/i&gt;, which are utilized to selfishly replicate themselves in the host germline genome. One rare example of ERVs that additionally carry &lt;i&gt;envelope&lt;/i&gt; genes is &lt;i&gt;Ty3/gypsy&lt;/i&gt; errantiviruses in &lt;i&gt;Drosophila&lt;/i&gt;. Though they are structurally analogous to retroviruses, it remained unclear whether &lt;i&gt;envelope&lt;/i&gt;-containing &lt;i&gt;Ty3/gypsy&lt;/i&gt; elements represent recent, lineage-specific acquisitions of viral fusogens or an ancient association between retrotransposons and &lt;i&gt;envelope&lt;/i&gt;-like genes. We systematically searched for intact &lt;i&gt;envelope&lt;/i&gt;-containing ERVs that are homologous to &lt;i&gt;Ty3/gypsy&lt;/i&gt; in invertebrate metazoan genomes and found that they are widespread across taxa, including ancient animals. such as cnidarians, ctenophores, and tunicates. Many elements occur as multiple highly similar copies in their respective genomes, consistent with recent genomic expansion in some host lineages. &lt;i&gt;Envelope&lt;/i&gt; genes are classified into those that resemble glycoprotein F from paramyxoviruses and glycoprotein B from herpesviruses, and both types are equally abundant and widespread. Phylogenetic and structural analyses revealed that &lt;i&gt;envelope&lt;/i&gt; genes have largely diverged with &lt;i&gt;pol&lt;/i&gt; genes as well as with the host organisms throughout their evolutionary history and recombined infrequently, suggesting that the &lt;i&gt;envelope&lt;/i&gt; acquisition to ERVs is ancient and likely dates to before the split of bilaterian and non-bilaterian animals in the Pre-Cambrian era.</description>
      <author>rippei.hayashi@anu.edu.au (Rippei Hayashi)</author>
      <author>rippei.hayashi@anu.edu.au (Shashank Chary)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.108449</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Fri, 28 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-28T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Evolution of sideways locomotion in crabs</title>
      <link>https://elifesciences.org/articles/110015</link>
      <description>The evolutionary change in the mode of locomotion is often a major evolutionary event, triggering diversification. Sideways locomotion is a defining feature of true crabs (Brachyura) and may have contributed to their ecological success. Yet, the evolutionary origin of this unique behavior remains unknown. Here, we show that the prevalence of sideways locomotion in true crabs reflects a single evolutionary origin from a forward-moving ancestor. Our behavioral analysis of 50 live crab species indicates that crab locomotion can be broadly separated into two predominant modes, sideways and forward locomotion. The phylogenetic comparative analysis revealed a single origin of sideways locomotion, with multiple independent reversions to forward locomotion in ecologically specialized groups. The species richness data show that the lineage in which sideways locomotion originated is far more diverse than its nearest outgroups. These results are consistent with the idea that sideways locomotion acted as a key innovation contributing to the evolutionary diversification of true crabs. Such a rare but innovative behavioral trait provides a framework for understanding how locomotor modes shape evolutionary diversification in animals.</description>
      <author>yuuki-k@nagasaki-u.ac.jp (Atsushi Hirai)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Fumio Takeshita)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Jung-Fu Huang)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Junya Taniguchi)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Kano Kohara)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Nobuaki Mizumoto)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Tsubasa Inoue)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Yuuki Kawabata)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110015</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Thu, 27 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-27T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Latent gene network expression underlies partial re-evolution of a polyphenic trait in the worker caste of ants</title>
      <link>https://elifesciences.org/articles/110148</link>
      <description>Polyphenisms–where alternative phenotypes develop from a single genome in response to environmental cues–are not only widespread in nature, but also occur at multiple levels of biological organization, from cells to individuals to societies. Polyphenism is thought to promote phenotypic diversification through the gain, loss, and re-evolution of alternative phenotypes. After the origin of a polyphenism, one of the alternative phenotypes often retains the developmental capacity to produce the ancestral trait, thereby permitting the other to evolve rapidly. Yet, little is known about the developmental processes underlying the re-evolution of polyphenic traits, and how they may produce phenotypic diversification. Here, we address this question by focusing on the caste polyphenism in ant societies, which produces a winged queen caste and a wingless worker caste in a single colony in response to environmental cues. We show, in a hyperdiverse group of ants, that a caste-specific trait called the ocelli (three simple eyes on the dorsal head) is always present across queen castes but was lost and partially re-evolved multiple times, giving rise to novel patterns (one ocelli) in the worker castes. Surprisingly, we discovered that a hidden (latent) expression of the ocelli gene regulatory network in worker castes that lost ocelli underlies the partial re-evolution of ocelli in this group. We therefore propose that latent developmental potentials may generally persist across polyphenic systems, including ant castes, and may facilitate the partial re-evolution of novel phenotypic patterns.</description>
      <author>abouheif@zju.edu.cn (Angelly Vasquez-Correa)</author>
      <author>abouheif@zju.edu.cn (Ehab Abouheif)</author>
      <author>abouheif@zju.edu.cn (Johanna Arnet)</author>
      <author>abouheif@zju.edu.cn (Travis Chen)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110148</guid>
      <category>Developmental Biology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 18 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-18T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Divergent &lt;i&gt;C. elegans&lt;/i&gt; toxin alleles are suppressed by distinct mechanisms</title>
      <link>https://elifesciences.org/articles/106269</link>
      <description>Toxin-antidote elements (TAs) are selfish DNA sequences that bias their transmission to the next generation. TAs typically consist of two linked genes: a toxin and an antidote. The toxin kills progeny that do not inherit the TA, while the antidote counteracts the toxin in progeny that inherit the TA. We previously discovered two TAs in &lt;i&gt;Caenorhabditis elegans&lt;/i&gt; that follow the canonical TA model of two linked genes: &lt;i&gt;peel-1/zeel-1&lt;/i&gt; and &lt;i&gt;sup-35/pha-1&lt;/i&gt;. Here, we report a new TA that exists in three distinct states across the &lt;i&gt;C. elegans&lt;/i&gt; population. The canonical TA, which is found in isolates from the Hawaiian Islands, consists of two genes that encode a maternally deposited toxin (TMRL-1) and a zygotically expressed antidote (AMRL-1). The toxin induces larval lethality in embryos that do not inherit the antidote gene. A second version of the TA has lost the toxin gene but retains a partially functional antidote. Most &lt;i&gt;C. elegans&lt;/i&gt; isolates, including the standard laboratory strain N2, carry a highly divergent allele of the toxin that has retained its activity, but have lost the antidote through pseudogenization. Multiple lines of evidence suggest that the N2 &lt;i&gt;tmrl-1&lt;/i&gt; allele is likely recognized by piRNAs, leading to MUT-16-dependent 22G small interfering RNA (siRNA) production and post-transcriptional silencing of the transcript. The N2 haplotype represents the first naturally occurring unlinked toxin-antidote system where the toxin is post-transcriptionally suppressed by endogenous small RNA pathways.</description>
      <author>szdralje@gmail.com (Daniel HW Leighton)</author>
      <author>szdralje@gmail.com (Giancarlo N Bruni)</author>
      <author>szdralje@gmail.com (Heriberto Marquez)</author>
      <author>szdralje@gmail.com (JB Collins)</author>
      <author>szdralje@gmail.com (Joshua S Bloom)</author>
      <author>szdralje@gmail.com (Laura Walter-McNeill)</author>
      <author>szdralje@gmail.com (Leonid Kruglyak)</author>
      <author>szdralje@gmail.com (Noah Alexander)</author>
      <author>szdralje@gmail.com (Stefan Zdraljevic)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.106269</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Tue, 11 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>The population structure of invasive &lt;i&gt;Lantana camara&lt;/i&gt; is shaped by its mating system</title>
      <link>https://elifesciences.org/articles/104988</link>
      <description>Over the last century, invasive species have emerged as an important driver of global biodiversity loss. &lt;i&gt;Lantana camara&lt;/i&gt; is one of the hundred most problematic invasive species globally, yet its genetic diversity patterns remain poorly understood. Previous studies hypothesize that invasive &lt;i&gt;L. camara&lt;/i&gt; is a species complex of hybrid origin, though this remains untested. We investigated the population genetic patterns of &lt;i&gt;L. camara&lt;/i&gt; by sampling 359 plants representing diverse flower colour variants across 36 locations in India. Analyses of the population structure using 19,008 SNPs revealed a strong genetic structure in India. However, this structure showed little correlation with geography; instead, individuals with similar flower colours clustered together irrespective of location in the structure analysis. Low genetic distance between most of the individuals indicated the absence of multiple species. A high inbreeding coefficient and low proportion of heterozygous sites suggested predominant self-fertilization, confirmed by bagging experiments. Thus, we infer that &lt;i&gt;L. camara&lt;/i&gt; exists as homozygous inbred lines formed by self-fertilization, associated with distinct flower colours. These results refute the hypothesis that &lt;i&gt;L. camara&lt;/i&gt; is a species complex. Our findings highlight a hitherto unknown role for mating systems in invasive species, furthering our understanding of evolution in invasive species.</description>
      <author>praveenprakash@ncbs.res.in (P Praveen)</author>
      <author>praveenprakash@ncbs.res.in (Rajesh Gopal)</author>
      <author>praveenprakash@ncbs.res.in (Uma Ramakrishnan)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104988</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Thu, 23 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-23T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>The adaptive landscapes of three global &lt;i&gt;Escherichia coli&lt;/i&gt; transcriptional regulators</title>
      <link>https://elifesciences.org/articles/103774</link>
      <description>The evolution of gene regulation is a major source of evolutionary adaptation and innovation, particularly when organisms encounter new or changing environments. Central to this process is the emergence of new transcription factor binding sites (TFBSs). Adaptive landscapes provide a powerful framework to study such emergence by linking regulatory DNA sequences to their transcriptional outputs. Although several landscapes have been characterized for DNA, RNA, and proteins, large-scale in vivo adaptive landscapes for bacterial TFBSs remain scarce. Here, we address this gap by experimentally mapping the first comprehensive in vivo regulatory landscapes for three global transcription factors in &lt;i&gt;Escherichia coli&lt;/i&gt;: cAMP receptor protein, Fis, and IHF. Using a massively parallel reporter assay, we quantify the regulation strength of more than 30,000 TFBS variants for each factor, and reconstruct their adaptive landscapes. All three landscapes are highly rugged and exhibit pervasive epistasis, with thousands of local peaks distributed broadly across sequence space. This ruggedness contrasts sharply with the much smoother TFBS landscapes of eukaryotes. It suggests greater constraints on the evolution of prokaryotic gene regulation. Nonetheless, evolutionary simulations show that ~10% of evolving populations can reach a peak of strong regulation, a proportion that is significantly greater than in comparable random landscapes. Adaptive evolution starting from the same DNA sequence can attain different high peaks, and some peaks are reached more frequently than others. Together, our results show that de novo adaptive evolution of new gene regulation in bacteria is feasible, but subject to a blend of chance, historical contingency, and evolutionary biases.</description>
      <author>caua.westmann@ieu.uzh.ch (Andreas Wagner)</author>
      <author>caua.westmann@ieu.uzh.ch (Cauã Antunes Westmann)</author>
      <author>caua.westmann@ieu.uzh.ch (Leander Goldbach)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103774</guid>
      <category>Evolutionary Biology</category>
      <category>Microbiology and Infectious Disease</category>
      <pubDate>Tue, 21 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-21T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Heterozygote advantage cannot explain MHC diversity, but MHC diversity can explain heterozygote advantage</title>
      <link>https://elifesciences.org/articles/107256</link>
      <description>Several theoretical studies have concluded that heterozygote advantage makes at most a minor contribution to MHC diversity. Siljestam and Rueffler (2024) recently presented models in which heterozygote advantage alone can lead to realistically high diversity. Here I argue that heterozygote advantage cannot by itself explain MHC diversity, and that its contribution to diversity is unlikely to be large in most species. I first show that the high diversity reported by Siljestam and Rueffler is so sensitive to parameter values that the underlying phenomenon cannot explain the widespread diversity of MHC genes. I then consider a fundamental problem with explaining MHC diversity by heterozygote advantage alone: selective forces that favored heterozygotes would lead to the evolution of haplotypes having much higher fitness when homozygous, diminishing or eliminating heterozygote advantage. Diversity maintained by another force, however, might bring about adaptation to the more common heterozygous state at the expense of homozygous fitness. Thus, substantial heterozygote advantage may arise as a consequence of MHC diversity.</description>
      <author>jcherry@ncbi.nlm.nih.gov (Joshua L Cherry)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107256</guid>
      <category>Evolutionary Biology</category>
      <category>Immunology and Inflammation</category>
      <pubDate>Mon, 13 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-13T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Correction: Asymmetrical diversification of the receptor-ligand interaction controlling self-incompatibility in Arabidopsis</title>
      <link>https://elifesciences.org/articles/112595</link>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.112595</guid>
      <category>Evolutionary Biology</category>
      <category>Plant Biology</category>
      <pubDate>Thu, 09 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-09T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Pervasive relaxed selection on spermatogenesis genes coincident with the evolution of polygyny in gorillas</title>
      <link>https://elifesciences.org/articles/94563</link>
      <description>Gorillas have a polygynous social system in which the highest-ranking male has almost exclusive access to females and sires most of the offspring in the troop. Such behavior results in a dramatic reduction of sperm competition, which is ultimately associated with numerous traits that cause low efficacy of gorilla spermatogenesis. However, the molecular basis behind the remarkable erosion of the gorilla male reproductive system remains unknown. Here, we explored the genetic implications of the polygynous social system in gorillas by testing for altered selection intensity across 13,310 orthologous protein-coding genes from 261 Eutherian mammals. We identified 578 genes with relaxed purifying selection in the gorilla lineage, compared with only 96 that were positively selected. Genes under relaxed purifying selection in gorillas have accumulated numerous deleterious amino acid substitutions; their expression is biased towards male germ cells, and they are enriched in functions related to meiosis and sperm biology. We tested the role of gorilla relaxed genes previously not implicated in male reproductive function using the &lt;i&gt;Drosophila&lt;/i&gt; model system and identified 41 novel spermatogenesis genes required for normal fertility. Furthermore, by exploring exome/genome sequencing data of infertile men with severe spermatogenic impairment, we found that the human orthologs of the gorilla relaxed genes are enriched for loss-of-function variants in infertile men. These data provide compelling evidence that reduced sperm competition in gorillas is associated with relaxed purifying selection on genes related to male reproductive function. The accumulation of deleterious mutations in these genes likely provides the mechanistic basis behind the low efficacy of gorilla spermatogenesis and uncovers new candidate genes for human male infertility.</description>
      <author>denard@arizona.edu (David Enard)</author>
      <author>denard@arizona.edu (Erik Schüftan)</author>
      <author>denard@arizona.edu (Frank Tüttelmann)</author>
      <author>denard@arizona.edu (Jacob D Bowman)</author>
      <author>denard@arizona.edu (Joana M Almeida)</author>
      <author>denard@arizona.edu (Neide Silva)</author>
      <author>denard@arizona.edu (Paulo Navarro-Costa)</author>
      <author>denard@arizona.edu (Raquel A Oliveira)</author>
      <author>denard@arizona.edu (Rion Brattig-Correia)</author>
      <author>denard@arizona.edu (Vincent J Lynch)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.94563</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Tue, 07 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-07T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Experimental evolution to thermal stress indicates climate resilience in a cosmopolitan arthropod</title>
      <link>https://elifesciences.org/articles/110352</link>
      <description>Adaptive evolution enables species to survive and thrive under changing environmental conditions. In the face of accelerating global climate change, thermal stress represents a major challenge to the persistence of terrestrial arthropods. Understanding the genetic mechanisms underlying thermal adaptation is therefore critical for predicting species’ evolutionary potential and future success. Here, we combine experimental evolution, phenotypic assays, and multi-omics analyses to investigate the adaptive responses of the diamondback moth (&lt;i&gt;Plutella xylostella&lt;/i&gt;), a globally destructive pest of cruciferous crops, to contrasting thermal environments. Populations evolved under hot (32 °C/27 °C) and cold (15 °C/10 °C) regimes exhibited distinct life history and fitness traits relative to those maintained under favorable conditions (26 °C). The hot strain showed accelerated development, higher fecundity, and increased survival under extreme heat, while the cold strain exhibited lower supercooling and freezing points, indicating enhanced cold hardiness. Integrated transcriptomic and metabolomic analyses revealed extensive transcriptional reprogramming and convergent metabolic adjustments, notably a reduction in lipid metabolism to conserve energy under thermal stress. Crucially, non-synonymous mutations in &lt;i&gt;PxSODC&lt;/i&gt; enhance superoxide scavenging efficiency, enabling effective oxidative stress management at lower gene expression levels. Furthermore, we identified epigenetic regulation via DNA methylation as a key mediator of this thermal tolerance. Together, these coordinated mutational, epigenetic, and metabolic insights highlight this arthropod’s capacity for global dispersal and likely persistence under climate change, establishing a framework for understanding equivalent effects in other species.</description>
      <author>sjyou@fafu.edu.cn (Fengluan Yao)</author>
      <author>sjyou@fafu.edu.cn (Gaoke Lei)</author>
      <author>sjyou@fafu.edu.cn (Geoff M Gurr)</author>
      <author>sjyou@fafu.edu.cn (Huiling Zhou)</author>
      <author>sjyou@fafu.edu.cn (Liette Vasseur)</author>
      <author>sjyou@fafu.edu.cn (Minsheng You)</author>
      <author>sjyou@fafu.edu.cn (Shijun You)</author>
      <author>sjyou@fafu.edu.cn (Yanting Chen)</author>
      <author>sjyou@fafu.edu.cn (Yating Duan)</author>
      <author>sjyou@fafu.edu.cn (Zongyao Ma)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110352</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 30 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-30T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Brawn before bite in endemic Asian eutherian mammals after the end-Cretaceous extinction</title>
      <link>https://elifesciences.org/articles/108917</link>
      <description>The first 10 million years (Myr) following the Cretaceous-Paleogene (K-Pg) mass extinction marked a period of global greenhouse conditions and dramatic rise of placental mammals. Because ~80% of known terrestrial sections capturing post-K-Pg mammal recovery come from North America, a substantial knowledge gap exists in the tempo and mode of recovery in Asia, where only 3% of global sites are located and most contain species found nowhere else. We show that isolated Paleocene eutherian assemblages from China (1) exhibited high mean tooth size and disparity early in the Paleocene, (2) shifted in their dental shape in parallel with regional and global environmental changes later in the Paleocene, and (3) achieved maximum dental shape-performance covariation near the end of the first 10 Myr post-K-Pg. This ‘brawn before bite’ transformation, coupled with prolonged dental shape versus performance variability, favors a scenario whereby many living orders of eutherian mammals were borne out of phenotypically and functionally plastic ancestral assemblages, including those in tropical South China, during the Paleocene.</description>
      <author>zjt@berkeley.edu (Qian Li)</author>
      <author>zjt@berkeley.edu (Suyin Ting)</author>
      <author>zjt@berkeley.edu (Z Jack Tseng)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.108917</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 30 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-30T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Constraints on the G1/S transition pathway may favor selection of multicellularity as a passenger phenotype</title>
      <link>https://elifesciences.org/articles/109833</link>
      <description>Multicellularity has emerged in the three branches of the tree of life. The formation of simple multicellular entities can either result from cells aggregating or staying together after mitosis. However, it is not yet fully understood how, once formed, these simple multicellular entities could be maintained or even selected for. Here, using the &lt;i&gt;ace2&lt;/i&gt; yeast snowflake model of simple multicellularity, we aimed at identifying genetic conditions favoring its maintenance. Growth-competition experiments revealed that, while the &lt;i&gt;ace2&lt;/i&gt; mutation by itself does not provide any fitness advantage or disadvantage, the &lt;i&gt;ace2&lt;/i&gt; snowflakes were strongly selected when combined with conditions affecting regulators of the G1/S transition of the cell cycle, such as Cln3 or Whi5. We show that this selection results from a faster exit from quiescence of the &lt;i&gt;ace2&lt;/i&gt; snowflake cells. Importantly, this advantage is not dependent on the multicellular phenotype, but rather on the &lt;i&gt;ace2&lt;/i&gt; genotype itself. We found that the &lt;i&gt;ace2&lt;/i&gt; selective advantage in the &lt;i&gt;cln3&lt;/i&gt; background fully depends on the &lt;i&gt;KSS1&lt;/i&gt; gene, a target of the Ace2 transcription factor. Finally, we show that phenotypes observed for &lt;i&gt;ace2&lt;/i&gt; mutants are phenocopied by the &lt;i&gt;AMN1&lt;sup&gt;368D&lt;/sup&gt;&lt;/i&gt; allelic form found in ‘non-laboratory’ yeast strains, hence adding physiological relevance to these observations. Altogether, our results support the hypothesis that simple multicellularity could, in some cases, persist, not because it provides a direct selective advantage due to multicellularity itself, but rather as a ‘passenger’ phenotype that is maintained alongside other selected traits.</description>
      <author>bertrand.daignan-fornier@u-bordeaux.fr (Bertrand Daignan-Fornier)</author>
      <author>bertrand.daignan-fornier@u-bordeaux.fr (Damien Laporte)</author>
      <author>bertrand.daignan-fornier@u-bordeaux.fr (Tom Louis Ducrocq)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109833</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Thu, 18 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-18T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Are interphylum spiralian relationships resolvable?</title>
      <link>https://elifesciences.org/articles/110607</link>
      <description>The phyla making up the major animal clade of Spiralia have been clear since the advent of molecular phylogenetics; the relationships between these spiralian phyla have not. The lack of consensus over the relationships between these important animal phyla might be a clue implying their emergence in an explosive radiation. Focussing on the five largest spiralian clades (Annelida, Brachiozoa, Mollusca, Nemertea, and Platyhelminthes) and using two phylogenomic datasets, we have applied site-bootstrapping and taxon-jackknifing to explore this example of taxonomic instability. Analyses of the 105 possible rooted trees relating them showed that interphylum branches are very short. Preference for rooting Spiralia on Platyhelminthes is enhanced by a long-branch artefact. Most analyses on the 15 unrooted trees showed a preference for the same topology but the support for this tree over other solutions was not significant. We conclude that the spiralian phyla emerged in rapid succession resulting in a difficult-to-resolve radiation. The deep history we infer for Spiralia has wide-ranging implications for our interpretation of Cambrian fossils and for the evolution of traits such as biomineralisation, segmentation, and larvae.</description>
      <author>m.telford@ucl.ac.uk (Ana Serra Silva)</author>
      <author>m.telford@ucl.ac.uk (Maximilian J Telford)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110607</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 16 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-16T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Faroese whole genomes provide insight into ancestry and recent selection</title>
      <link>https://elifesciences.org/articles/107428</link>
      <description>The Faroe Islands are home to descendants of a North Atlantic founder population with a unique history shaped by both migration and periods of relative isolation. Here, we investigate the genetic diversity, population structure, and demographic history of the islands by analyzing whole genome sequencing data from 40 participants in the Faroe Genome Project. This represents the first whole genome sequencing panel of this size from the Faroe Islands. We observed numerous putatively functional private alleles, including stop gain variants and high impact missense variants in the cohort. Faroese individuals had a higher proportion of their genomes contained in long runs of homozygosity than other European groups, including Finnish, suggesting a more recent or stronger bottleneck in the Faroese population. Signals of positive selection were identified at loci containing genes that play roles in vitamin D and dietary fat absorption and DNA repair, while increased diversity on lactase persistence haplotypes was observed. Fine-scale analysis of haplotype structure in present-day and ancient European genomes revealed genetic affinities with ancient Iron Age individuals from the North and West of Europe, providing evidence for potential contributions to the Faroese gene pool from Celtic and Viking populations as well as information about the temporal order in which these events happened. This study highlights the impact of evolutionary processes, such as ancient admixture, founder events, and positive selection, on the present-day genetic architecture of North Atlantic founder populations like the Faroe Islands.</description>
      <author>fracimo@sund.ku.dk (Alba Refoyo-Martínez)</author>
      <author>fracimo@sund.ku.dk (Anne-Katrin Emde)</author>
      <author>fracimo@sund.ku.dk (Fernando Racimo)</author>
      <author>fracimo@sund.ku.dk (Guðrið Andorsdóttir)</author>
      <author>fracimo@sund.ku.dk (Iman Hamid)</author>
      <author>fracimo@sund.ku.dk (Jonas Meisner)</author>
      <author>fracimo@sund.ku.dk (Kaja A Wasik)</author>
      <author>fracimo@sund.ku.dk (Katrin D Apol)</author>
      <author>fracimo@sund.ku.dk (Leivur N Lydersen)</author>
      <author>fracimo@sund.ku.dk (Melissa Hendershott)</author>
      <author>fracimo@sund.ku.dk (Noomi O Gregersen)</author>
      <author>fracimo@sund.ku.dk (Ólavur Mortensen)</author>
      <author>fracimo@sund.ku.dk (Stephane E Castel)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107428</guid>
      <category>Evolutionary Biology</category>
      <category>Genetics and Genomics</category>
      <pubDate>Tue, 16 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-16T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Host and antibiotic jointly select for greater virulence in &lt;i&gt;Staphylococcus aureus&lt;/i&gt;</title>
      <link>https://elifesciences.org/articles/107936</link>
      <description>Widespread antibiotic usage has resulted in the rapid evolution of drug-resistant bacterial pathogens. Resolving how pathogens respond to antibiotics under different contexts is critical for understanding disease emergence. It remains unclear how interactions between hosts and antibiotics impact pathogen evolution. Here, we evolved &lt;i&gt;Staphylococcus aureus,&lt;/i&gt; a major bacterial pathogen, varying exposure to host and antibiotics to tease apart the contributions of these selective pressures on pathogen adaptation. After 12 passages, &lt;i&gt;S. aureus&lt;/i&gt; evolving in &lt;i&gt;Caenorhabditis elegans&lt;/i&gt; nematodes exposed to a sub-minimum inhibitory antibiotic concentration became highly virulent, regardless of whether the ancestral pathogen was methicillin-resistant (MRSA) or methicillin-sensitive (MSSA). Host and antibiotic selected for reduced drug susceptibility in MSSA while increasing MRSA total growth outside hosts. We identified mutations in genes involved in regulatory networks linking virulence and metabolism, suggesting that rapid adaptation to infect hosts may have pleiotropic effects. Mutations that arose in these genes were also enriched in clinical isolates associated with systemic infections in humans. Despite evolving in similar environments, MRSA and MSSA populations—differing only in the presence of an intact accessory gene—proceeded on divergent evolutionary paths, with MSSA populations exhibiting more similarities across replicates. Our results underscore the importance of the host context as a driver of virulence and antibiotic resistance.</description>
      <author>tread@emory.edu (Jennifer D Gresham)</author>
      <author>tread@emory.edu (Kim L Hoang)</author>
      <author>tread@emory.edu (Levi T Morran)</author>
      <author>tread@emory.edu (McKenna Penley)</author>
      <author>tread@emory.edu (Michelle H Davis)</author>
      <author>tread@emory.edu (Michelle Su)</author>
      <author>tread@emory.edu (Timothy D Read)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107936</guid>
      <category>Evolutionary Biology</category>
      <category>Microbiology and Infectious Disease</category>
      <pubDate>Tue, 16 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-16T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Distinct evolutionary trajectories of two integration centres, the central complex and mushroom bodies, across Heliconiini butterflies</title>
      <link>https://elifesciences.org/articles/107589</link>
      <description>Neural circuits evolved to produce variable cognitive processes through adaptive mechanisms operating within a background of developmental and functional constraints. Understanding how this conflict is resolved requires a comparative framework encapsulating clear behavioural variation. We leverage Heliconiini butterflies to examine how selection shaped the evolution of the central complex and mushroom bodies, two insect integration centres involved in navigation. The evolution of systematic spatial foraging in &lt;i&gt;Heliconius&lt;/i&gt; has led to changes in brain morphology and learning and memory profiles over a short evolutionary timescale. Here, we show that in contrast to massively expanded mushroom bodies, the central complex is strongly conserved in size and general architecture. However, we identify divergences in the expression of a neuropeptide, Allatostatin A, in the noduli, and in the numbers of GABA-ergic ring neurons and their branching in the fan-shaped body, which are essential members of the anterior compass pathway. These differences are rare examples of divergence inside the central complex network matching expectations of where evolutionary adaptability might occur. We conclude that due to the contrasting volumetric conservation of the central complex, and the massive differences in the mushroom bodies, their circuit logics must determine distinct responses to selection associated with divergent foraging behaviours.</description>
      <author>m.farnworth@bristol.ac.uk (Basil el Jundi)</author>
      <author>m.farnworth@bristol.ac.uk (Elizabeth A Hodge)</author>
      <author>m.farnworth@bristol.ac.uk (Max S Farnworth)</author>
      <author>m.farnworth@bristol.ac.uk (Stephen H Montgomery)</author>
      <author>m.farnworth@bristol.ac.uk (Theodora Loupasaki)</author>
      <author>m.farnworth@bristol.ac.uk (Yi Peng Toh)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107589</guid>
      <category>Evolutionary Biology</category>
      <category>Neuroscience</category>
      <pubDate>Mon, 01 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-01T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Rapid riparian ecosystem recovery in low-latitudinal North China following the end-Permian mass extinction</title>
      <link>https://elifesciences.org/articles/104205</link>
      <description>The greatest mass extinction at the end of the Permian, ca. 252 million years ago, led to a tropical dead zone on land and sea. The speed of recovery of life has been debated, whether fast or slow, and terrestrial ecosystems are much less understood than marine. Here, we show fast reestablishment of riparian ecosystems in low-latitude North China as little as ~2 million years after the end-Permian mass extinction. The initial ichnoassemblages in shallow lacustrine and fluvial facies of late Smithian age are monospecific, devoid of infaunalization, with apparent size reduction. In the following Spathian, relatively complex, multi-level, structured riverain ecosystems had been rebuilt including medium-sized carnivores, plant stems, root traces, increased ichnological complexity, and significantly increased infaunalization. Specifically, burrowing behavior had re-emerged as a key life strategy not only to minimize stressful climatic conditions, but possibly to escape predation.</description>
      <author>tianlibgeg@cug.edu.cn (Daoliang Chu)</author>
      <author>tianlibgeg@cug.edu.cn (Jinnan Tong)</author>
      <author>tianlibgeg@cug.edu.cn (Jun Liu)</author>
      <author>tianlibgeg@cug.edu.cn (Li Tian)</author>
      <author>tianlibgeg@cug.edu.cn (Michael J Benton)</author>
      <author>tianlibgeg@cug.edu.cn (Wenchao Shu)</author>
      <author>tianlibgeg@cug.edu.cn (Wenwei Guo)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104205</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Mon, 18 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-18T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Recombination shapes the diversification of the &lt;i&gt;wtf&lt;/i&gt; meiotic drivers</title>
      <link>https://elifesciences.org/articles/100638</link>
      <description>Meiotic drivers are selfish genetic elements that distort fair segregation. The &lt;i&gt;wtf&lt;/i&gt; genes are poison-antidote meiotic drivers that are experiencing rapid diversification in fission yeasts. However, gene duplication alone is insufficient to drive the diversification of &lt;i&gt;wtf&lt;/i&gt; genes, given the poison encoded by a newly duplicated &lt;i&gt;wtf&lt;/i&gt; gene can be detoxified by the antidote encoded by the original &lt;i&gt;wtf&lt;/i&gt; gene. Here, we analyze the evolution of &lt;i&gt;wtf&lt;/i&gt; genes across 21 strains of &lt;i&gt;Schizosaccharomyces pombe&lt;/i&gt;. Knocking out each of 25 &lt;i&gt;wtf&lt;/i&gt; genes in &lt;i&gt;S. pombe&lt;/i&gt; strain 972h- separately does not attenuate the yeast growth, indicating that the &lt;i&gt;wtf&lt;/i&gt; genes might be largely neutral to their carriers in asexual life cycle. Interestingly, &lt;i&gt;wtf&lt;/i&gt; genes underwent recurrent and intricate recombination. As proof of principle, we generate a novel meiotic driver through artificial recombination between &lt;i&gt;wtf&lt;/i&gt; drivers, and its encoded poison cannot be detoxified by the antidotes encoded by their parental &lt;i&gt;wtf&lt;/i&gt; genes but can be detoxified by its own antidote. Therefore, we propose that recombination can generate new meiotic drivers and thus shape the diversification of the &lt;i&gt;wtf&lt;/i&gt; drivers.</description>
      <author>gongzhen@nnu.edu.cn (Guan-Zhu Han)</author>
      <author>gongzhen@nnu.edu.cn (Hao Xu)</author>
      <author>gongzhen@nnu.edu.cn (Qinliu He)</author>
      <author>gongzhen@nnu.edu.cn (Yan Wang)</author>
      <author>gongzhen@nnu.edu.cn (Zhen Gong)</author>
      <author>gongzhen@nnu.edu.cn (Zhiwei Wu)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.100638</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Mon, 11 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Investments in photoreceptors compete with investments in optics to determine eye design</title>
      <link>https://elifesciences.org/articles/96517</link>
      <description>Eyes provide opportunities to understand the function, design, development, and evolution of elaborate sense organs. We take a new cost–benefit approach to understanding eye design by considering that optics and photoreceptors compete for the resources invested in an integrated system. We investigate this competition theoretically and empirically using a new measure of cost, specific volume. This common currency for optics and photoreceptors relates investments to image quality via geometrical, optical, and physiological constraints. By covering the morphospace of an eye of given type and cost, we model how trading optics against photoreceptors changes information capacity. In apposition compound eyes and simple eyes, an optimum configuration maximises efficiency. Efficiency requires heavy investment in photoreceptors and depends on photoreceptor energy consumption. Optimum information capacities and efficiencies scale non-linearly with total investment. Diurnal insects’ apposition eyes follow trends that promote efficiency: photoreceptor arrays take 40–80% of total specific volume, photoreceptor length increases systematically with spatial resolution, and photoreceptors are exceptionally long. Thus, competition between optics and photoreceptors shapes eye design, and matching investments in optics and photoreceptors to improve efficiency is a design principle. Our new methodology can be developed to view the adaptive radiation of eyes through a cost–benefit lens.</description>
      <author>SL104@cam.ac.uk (Francisco JH Heras)</author>
      <author>SL104@cam.ac.uk (Simon B Laughlin)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.96517</guid>
      <category>Evolutionary Biology</category>
      <category>Neuroscience</category>
      <pubDate>Tue, 05 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-05T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Inference of germinal center evolutionary dynamics via simulation-based deep learning</title>
      <link>https://elifesciences.org/articles/108880</link>
      <description>B cells and the antibodies they produce are vital to health and survival, motivating research on the details of the mutational and evolutionary processes in the germinal centers (GCs) from which mature B cells arise. It is known that B cells with higher affinity for their cognate antigen (Ag) will, on average, tend to have more offspring. However, the exact form of this relationship between affinity and fecundity, which we call the ‘affinity–fitness response function’, is not known. Here we use deep learning and simulation-based inference to learn this function from a unique experiment that replays a particular combination of GC conditions many times in mice. All code is freely available at &lt;a href="https://github.com/matsengrp/gcdyn"&gt;https://github.com/matsengrp/gcdyn&lt;/a&gt;, while datasets and inference results can be found at &lt;a href="https://doi.org/10.5281/zenodo.15022130"&gt;https://doi.org/10.5281/zenodo.15022130&lt;/a&gt;.</description>
      <author>dralph@fredhutch.org (Ashni A Vora)</author>
      <author>dralph@fredhutch.org (Athanasios G Bakis)</author>
      <author>dralph@fredhutch.org (Duncan K Ralph)</author>
      <author>dralph@fredhutch.org (Frederick A Matsen)</author>
      <author>dralph@fredhutch.org (Gabriel D Victora)</author>
      <author>dralph@fredhutch.org (Jared G Galloway)</author>
      <author>dralph@fredhutch.org (Tatsuya Araki)</author>
      <author>dralph@fredhutch.org (William S DeWitt)</author>
      <author>dralph@fredhutch.org (Yun S Song)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.108880</guid>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 28 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-28T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Taking the biology seriously makes models better</title>
      <link>https://elifesciences.org/articles/111070</link>
      <description>A new biologically-informed training paradigm enables protein language models to predict affinity maturation trajectories for antibodies.</description>
      <author>a.gil@ucl.ac.uk (Andreas Tiffeau-Mayer)</author>
      <author>a.gil@ucl.ac.uk (Antonio Matas-Gil)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.111070</guid>
      <category>Evolutionary Biology</category>
      <category>Immunology and Inflammation</category>
      <pubDate>Mon, 20 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-20T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Adaptive variation in avian eggshell gas conductance and structure across elevational gradients?</title>
      <link>https://elifesciences.org/articles/85564</link>
      <description>Many tropical bird species have restricted elevational distributions, potentially limited by how environmental conditions affect physiological processes. While some studies have examined adult physiology across elevations, relatively little attention has been given to the structure and function of eggshells despite their critical role in regulating gas exchange during the vulnerable embryonic stage. At high elevations, dry air is expected to increase water loss from the egg, and natural selection may favor lower gas conductance to reduce desiccation risk. Structural variation in eggshells, such as increased shell thickness or reduced pore size and density, could serve as a mechanism to regulate gas diffusion. To test for adaptive variation in eggshell traits along elevational gradients, we measured water vapor conductance and used scanning electron microscopy (SEM) to examine eggshell structure in 197 bird species from the Andes. We found that water vapor conductance declined at high elevations across avian communities. However, structural changes in eggshells varied among bird families and did not vary in a predictable way with elevation, suggesting no relationship or divergent adaptive responses to shared selective pressures, particularly in shell thickness, pore density, and pore size. We propose that examining functional and structural eggshell traits can offer insight into species’ elevational limits and inform predictions about their responses to climate change.</description>
      <author>docampo@princeton.edu (Carlos Daniel Cadena)</author>
      <author>docampo@princeton.edu (David Ocampo)</author>
      <author>docampo@princeton.edu (Esteban Correa-Agudelo)</author>
      <author>docampo@princeton.edu (Gustavo A Londoño)</author>
      <author>docampo@princeton.edu (Marcela Hernández Hoyos)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.85564</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 14 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-14T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Identification and comparison of orthologous cell types from primate embryoid bodies shows limits of marker gene transferability</title>
      <link>https://elifesciences.org/articles/105398</link>
      <description>The identification of cell types remains a major challenge. Even after a decade of single-cell RNA sequencing (scRNA-seq), reasonable cell type annotations almost always include manual non-automated steps. The identification of orthologous cell types across species complicates matters even more, but at the same time strengthens the confidence in the assignment. Here, we generate and analyze a dataset consisting of embryoid bodies (EBs) derived from induced pluripotent stem cells (iPSCs) of four primate species: humans, orangutans, cynomolgus, and rhesus macaques. This kind of data includes a continuum of developmental cell types, multiple batch effects (i.e. species and individuals) and uneven cell type compositions and hence poses many challenges. We developed a semi-automated computational pipeline combining classification and marker-based cluster annotation to identify orthologous cell types across primates. This approach enabled the investigation of cross-species conservation of gene expression. Consistent with previous studies, our data confirm that broadly expressed genes are more conserved than cell type-specific genes, raising the question of how conserved, inherently cell type-specific, marker genes are. Our analyses reveal that human marker genes are less effective in macaques and vice versa, highlighting the limited transferability of markers across species. Overall, our study advances the identification of orthologous cell types across species, provides a well-curated cell type reference for future in vitro studies and informs the transferability of marker genes across species.</description>
      <author>enard@bio.lmu.de (Anita Térmeg)</author>
      <author>enard@bio.lmu.de (Beate Vieth)</author>
      <author>enard@bio.lmu.de (Fiona C Edenhofer)</author>
      <author>enard@bio.lmu.de (Ines Hellmann)</author>
      <author>enard@bio.lmu.de (Jessica Jocher)</author>
      <author>enard@bio.lmu.de (Johanna Geuder)</author>
      <author>enard@bio.lmu.de (Paulina Spurk)</author>
      <author>enard@bio.lmu.de (Philipp Janssen)</author>
      <author>enard@bio.lmu.de (Tamina Dietl)</author>
      <author>enard@bio.lmu.de (Wolfgang Enard)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105398</guid>
      <category>Computational and Systems Biology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Wed, 08 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-08T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Fitness drivers of division of labor in vertebrates</title>
      <link>https://elifesciences.org/articles/105501</link>
      <description>Although division of labor as a means to increase productivity is a common feature in animal social groups, most previous studies have focused almost exclusively on eusocial insects with extreme task partitioning. Empirical evidence of division of labor in vertebrates is scarce, largely because we lack a theoretical framework to explore the conditions under which division of labor is likely to evolve in cooperatively breeding systems where helpers remain capable of breeding throughout their lifetime. By explicitly considering alternative helping tasks with varying fitness costs, we model how individual decisions on task specialization may influence the emergence of division of labor under both direct and indirect fitness benefits. Surprisingly, we find that direct survival benefits of living in larger groups are the primary force driving the evolution of cooperation to enhance group productivity, and that indirect fitness benefits derived from related group members are only a non-essential facilitator of more stable forms of division of labor in cooperative breeders. In addition, we find that division of labor in vertebrates is favored by harsh environments. Ultimately, our model not only makes key predictions that are consistent with existing empirical data, but also proposes novel avenues for new empirical work in vertebrate and invertebrate systems alike.</description>
      <author>igaru.13@gmail.com (Dustin R Rubenstein)</author>
      <author>igaru.13@gmail.com (Irene García-Ruiz)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105501</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Wed, 08 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-08T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Separating selection from mutation in antibody language models</title>
      <link>https://elifesciences.org/articles/109644</link>
      <description>Antibodies are encoded by nucleotide sequences that are generated by V(D)J recombination and evolve according to mutation and selection processes. Existing antibody language models, however, focus exclusively on antibodies as strings of amino acids and are fitted using standard language modeling objectives such as masked or autoregressive prediction. In this paper, we first show that fitting models using this objective implicitly incorporates nucleotide-level mutation processes as part of the protein language model, which degrades performance when predicting effects of mutations on functional properties of antibodies. To address this limitation, we devise a new framework: a deep amino acid selection model (DASM) that learns the selection effects of amino acid mutations while explicitly factoring out the nucleotide-level mutation process. By fitting selection as a separate term from the mutation process, the DASM exclusively quantifies functional effects: effects that change some aspect of the function of the antibody. This factorization leads to substantially improved performance on standard functional benchmarks. Moreover, our model is an order of magnitude smaller and multiple orders of magnitude faster to evaluate than existing approaches, as well as being readily interpretable.</description>
      <author>matsen@fredhutch.org (David H Rich)</author>
      <author>matsen@fredhutch.org (Frederick A Matsen IV)</author>
      <author>matsen@fredhutch.org (Hugh K Haddox)</author>
      <author>matsen@fredhutch.org (Julia Fukuyama)</author>
      <author>matsen@fredhutch.org (Kevin Sung)</author>
      <author>matsen@fredhutch.org (Mackenzie M Johnson)</author>
      <author>matsen@fredhutch.org (Tyler N Starr)</author>
      <author>matsen@fredhutch.org (Will Dumm)</author>
      <author>matsen@fredhutch.org (Yun S Song)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109644</guid>
      <category>Evolutionary Biology</category>
      <category>Immunology and Inflammation</category>
      <pubDate>Tue, 07 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-07T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Human genetic ancestry, &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt; diversity, and tuberculosis disease severity in Dar es Salaam, Tanzania</title>
      <link>https://elifesciences.org/articles/103533</link>
      <description>Infectious diseases have affected humanity for millennia and are among the strongest selective forces. Tuberculosis (TB) is an ancient disease, caused by the human-adapted members of the &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt; complex (MTBC). The outcome of TB infection and disease is highly variable, and co-evolution between human populations and MTBC strains may account for some of this variability. Particular human genetic ancestries have been associated with higher susceptibility to TB, but sociodemographic aspects of the disease can confound such associations. Here, we studied 1000 TB patients from Dar es Salaam, Tanzania, together with their respective MTBC isolates, by combining human and bacterial genomics with clinical data. We found that the genetic background of the TB patient population was strongly influenced by migrations of Bantu-speaking populations from West Africa, which contrasts with the corresponding MTBC genotypes that were mainly introduced from outside Africa. These findings suggest a recent evolutionary history of co-existence between the human and MTBC populations in Dar es Salaam. We detected no evidence of an effect of human genetic ancestry, or MTBC phylogenetic diversity alone, nor their interaction, on TB disease severity. There was also no evidence of an association between human variation genome-wide and TB disease severity. Treatment-seeking, social, and environmental factors are likely to be the main determinants of disease severity at the point of care in this patient population.</description>
      <author>sebastien.gagneux@swisstph.ch (Amanda Ross)</author>
      <author>sebastien.gagneux@swisstph.ch (Damien Portevin)</author>
      <author>sebastien.gagneux@swisstph.ch (Daniela Brites)</author>
      <author>sebastien.gagneux@swisstph.ch (Hellen Charles Hiza)</author>
      <author>sebastien.gagneux@swisstph.ch (Jacques Fellay)</author>
      <author>sebastien.gagneux@swisstph.ch (Jerry Hella)</author>
      <author>sebastien.gagneux@swisstph.ch (Klaus Reither)</author>
      <author>sebastien.gagneux@swisstph.ch (Liliana K Rutaihwa)</author>
      <author>sebastien.gagneux@swisstph.ch (Lluis Quintana-Murci)</author>
      <author>sebastien.gagneux@swisstph.ch (Maxime Rotival)</author>
      <author>sebastien.gagneux@swisstph.ch (Michaela Zwyer)</author>
      <author>sebastien.gagneux@swisstph.ch (Mohamed Sasamalo)</author>
      <author>sebastien.gagneux@swisstph.ch (Sebastien Gagneux)</author>
      <author>sebastien.gagneux@swisstph.ch (Sonia Borrell)</author>
      <author>sebastien.gagneux@swisstph.ch (Zhi Ming Xu)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103533</guid>
      <category>Evolutionary Biology</category>
      <category>Microbiology and Infectious Disease</category>
      <pubDate>Tue, 24 Mar 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-03-24T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Developmental, regenerative, and behavioral dynamics in acoel reproduction</title>
      <link>https://elifesciences.org/articles/105712</link>
      <description>Acoel worms are an enigmatic and understudied animal lineage. Sparse descriptions suggest a diversity of reproductive anatomies across acoels, and likely a corresponding behavioral diversity. Here, we study the reproductive life history of the acoel &lt;i&gt;Hofstenia miamia&lt;/i&gt;, an emerging lab-tractable model system. We describe &lt;i&gt;H. miamia&lt;/i&gt;’s reproductive organs, identifying structures previously unknown in acoels. Following worms from zygotes to adulthood, we find that their reproductive organs emerge in a stereotyped sequence as a function of increasing body size. These organs regenerate in a similar sequence after major injuries and are lost in the opposite sequence during starvation-induced de-growth, suggesting that organ growth may be regulated by a single, size-associated program in all contexts. Studying egg-laying behavior, we find that &lt;i&gt;H. miamia&lt;/i&gt; lay their eggs through their mouths after loading them into their pharynges. Worms lay eggs for months after a single mating, suggesting long-term sperm storage despite lacking a storage organ. They can also lay viable eggs without mating, indicating a capacity for self-fertilization. Finally, worms assess past and present environmental features during egg-laying decisions, frequently laying eggs in communal clutches. Together, our work establishes foundational knowledge for the study of reproductive development, physiology, and behavior in acoels.</description>
      <author>vchandra1@fas.harvard.edu (Allison P Kann)</author>
      <author>vchandra1@fas.harvard.edu (Diana Marcela Bolanos)</author>
      <author>vchandra1@fas.harvard.edu (Mansi Srivastava)</author>
      <author>vchandra1@fas.harvard.edu (Samantha Elizabeth Tseng)</author>
      <author>vchandra1@fas.harvard.edu (Vikram Chandra)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105712</guid>
      <category>Developmental Biology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Fri, 20 Mar 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-03-20T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
  </channel>
</rss>
