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ABSTRACT In Euthyneuran molluscs, the distribution and plethora of dopamine (DA) functions are likely coupled to the feeding ecology with a broad spectrum of modifications both in the central and peripheral neural systems. However, studies of benthic grazers currently dominate the analysis of DA‐mediated signaling, whereas adaptations to pelagic lifestyles and other feeding strategies are unknown. Here, we characterize the distribution of central and peripheral neurons in representatives of distinct ecological groups: the pelagic predatory pteropodClione limacina(Pteropoda, Gymnosomata) and its prey —Limacina helicina(Pteropoda, Thecosomata), as well as the plankton eaterMelibe leonina(Nudipleura, Nudibranchia). By using tyrosine hydroxylase immunoreactivity as a reporter, we mapped their dopaminergic systems. Across all studied species, despite their differences in ecology, small numbers of dopaminergic neurons in the central ganglia contrast to an incredible density of these neurons in the peripheral nervous system, primarily representing sensory‐like cells, which are predominantly concentrated in the chemotactic areas and project afferent axons to the central nervous system. Combined with tubulin immunoreactivity, this study illuminates the complexity of sensory signaling and peripheral neural systems in Euthyneuran molluscs with lineage‐specific adaptations across different taxonomical and ecological groups. 

Exploring the evolutionary dynamics of lysozymes is critical for advancing our knowledge of adaptations in immune and digestive systems. Here, we characterize the distribution of a unique class of lysozymes known as g-type, which hydrolyze key components of bacterial cell walls. Notably, ctenophores, and choanoflagellates (the sister group of Metazoa), lack g-type lysozymes. We reveal a mosaic distribution of these genes, particularly within lophotrochozoans/spiralians, suggesting the horizontal gene transfer events from predatory myxobacteria played a role in their acquisition, enabling specialized dietary and defensive adaptations. We further identify two major groups of g-type lysozymes based on their widespread distribution in gastropods. Despite their sequence diversity, these lysozymes maintain conserved structural integrity that is crucial for enzymatic activity, underscoring independent evolutionary pathways where g-type lysozymes have developed functionalities typically associated with different lysozyme types in other species. Specifically, usingAplysia californicaas a reference species, we identified three distinct g-type lysozyme genes: two are expressed in organs linked to both feeding and defense, and the third exhibits broader distribution, likely associated with immune functions. These findings advance our understanding of the evolutionary dynamics shaping the recruitment and mosaic functional diversification of these enzymes across metazoans, offering new insights into ecological physiology and physiological evolution as emerging fields. 

Genomic blueprints underlying unique neuronal organization are enigmatic. A new study reveals the recruitment of ancient, larger genes for synaptic machinery, providing evolutionary constraints and flexibility, with increasing gene sizes being found in animal lineages that led to cephalopods and vertebrates.