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Komaki, F.

Publications and source records attributed to Komaki, F..

2 recordsLinked to original sources

Inferring community architectures of multisensory pathways in Drosophila via unsupervised network embedding

Understanding the complex architecture and functions of neural circuits is central to unraveling the mechanisms of multisensory integration. In this study, we analyzed the structural properties of the Drosophila adult brain to infer community structures within multisensory pathways. We adopt a network embedding method developed by ourselves, the Bidirectional Heterogeneous Graph Neural Network with Random Teleport (BHGNN-RT), designed to generate vector representations of neurons in a directed, heterogeneous brain connectome. This approach takes advantage of both structural connectivity and network heterogeneity features, enabling effective clustering of neurons and revealing hierarchical community architectures in olfactory and broader multisensory systems. We applied BHGNN-RT to the fly brain connectome to examine connectivity-based community organization in major neuronal classes along multisensory pathways, revealing distinct neural groups with unique connectivity patterns in the antennal lobe, lateral horn, mushroom body, and other brain regions. Further analysis showed how different neural groups contribute to the integration of sensory information in olfactory and multisensory systems. We also investigated the bilateral symmetry of the olfactory pathway, shedding light on how sensory signals are processed with ipsilateral and contralateral connections to ensure robust perception. Our findings demonstrate the utility of graph representation learning in analyzing the structural connectivity of complex neural systems. The insights gained from BHGNN-RT provide a deeper understanding of the community architecture in the Drosophila brain and contribute to a broader comprehension of the mechanisms underlying multisensory integration.

bioinformatics↗

Paternal aging affects the developmental patterns of ultrasonic vocalization induced by maternal separation in neonatal mice individually

Infant crying is an innate communicative behavior that is frequently impaired in certain neurodevelopmental disorders (NDDs). Since advanced paternal age is a reported risk factor for NDDs in offspring, we evaluated the impact of a fathers age on early vocal development in C57BL/6J mice. We recorded and applied a unique combination of computational analyses to ultrasonic vocalizations (USVs) emitted by mouse pups sired by young and aged fathers. Our data showed that advanced paternal age reduced the number and duration of USVs, and altered the syllable composition in pups. Moreover, pups born to young fathers showed convergent vocal characteristics with a rich repertoire during postnatal development, while those born to aged fathers exhibited more divergent vocal patterns with limited repertoire. Principal component analysis in conjunction with clustering analysis demonstrated that pups from aged fathers deviated from typical trajectories of vocal development, which were considered as atypical individuals. Thus, our study indicates that advanced paternal age has a significant effect on offsprings early vocal development. It is suggested that the trajectories of vocal development could be a useful marker of the NDD-like phenotype associated with the advanced paternal age. In addition, our comprehensive computational analysis described here is an effective approach to characterize the altered individual diversity relevant to neurodevelopmental disorders. One Sentence SummaryAdvanced paternal age affects vocal development in early postnatal mice, with more pups showing atypical developmental trajectories.

neuroscience↗