Modular organization and selective motifs in the insula provide structural priors for efficient learning

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Abstract

The insular cortex (IC) integrates diverse sensory and interoceptive signals to support emotional and cognitive functions, exhibiting topologically functional distinctions. Although long-range pathways of the IC have been extensively mapped, the contribution of intra-IC architecture to network-level information processing remains poorly understood. Here we reconstructed single-cell projectomes of 2,267 IC neurons, generating a comprehensive cellular-resolution map of intra-IC connectivity. Graph-theoretic analyses revealed a hierarchical, topographically organized modular network with a hub-and-spoke organization and selective motif enrichment. Embedding these anatomical priors into recurrent neural network models demonstrated that intrinsic IC topology confers a distinct computational advantage: across multiple cognitive tasks, IC-initialized networks learned faster and exhibited better robustness to perturbations than those initialized with shuffled, randomized, or neighboring somatosensory cortical architectures. Together, these findings identify the IC as a structurally specialized cortical hub whose internal wiring supports efficient learning and provides design principles for brain-inspired networks.

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