DCX knockout ferret reveals a neurogenic mechanism in cortical development

Lissencephaly is a rare brain malformation for which our understanding remains limited due to the absence of suitable animal models that accurately represent human phenotypes. Here, we establish doublecortin (DCX) knockout ferrets as a model that faithfully replicates key features of the disorder. We reveal the critical roles of DCX in neural progenitor cell proliferation and radial glial fiber extension, processes essential for normal cortical development. Utilizing single-nucleus RNA sequencing (snRNA-seq) and spatial transcriptomics, we provide a detailed atlas of the lissencephalic cortex, illustrating disrupted neuronal lamination and the specific interactions between inhibitory and excitatory neurons. These findings enhance our understanding of the cellular and molecular mechanisms underlying lissencephaly and highlight the potential of DCX knockout ferrets as a valuable tool for neurodevelopmental research, offering insights into both the pathology of lissencephaly and the general principles of brain development. [Display omitted] •DCX ferrets mimic human lissencephaly syndrome•DCX is crucial for NPC proliferation and fiber extension•Atlas of lissencephalic cortex via snRNA-seq•Specific coupling of inhibitory to excitatory neurons Wang et al. demonstrate that DCX knockout ferrets mirror human lissencephaly phenotypes, shedding light on disrupted neuronal lamination and neurogenesis. The study employs snRNA-seq and spatial transcriptomics to provide a detailed cellular and molecular landscape of the affected brain.