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The generation of suitable animal models for ALS is essential for understanding its pathogenesis and developing therapies. Therefore, we used CRISPR-Cas9 to generate FUS-ALS mutation in the non-classical nuclear localization signal (NLS), H517D (mouse position: H509D) and genome-edited mice.<\/jats:p>\n               <jats:p>Fus WT\/H509D mice showed progressive motor impairment (accelerating rotarod and DigiGait system) with age, which was associated with the loss of motor neurons and disruption of the nuclear lamina and nucleoporins and DNA damage in spinal cord motor neurons. We confirmed the validity of our model by showing that nuclear lamina and nucleoporin disruption were observed in lower motor neurons differentiated from patient-derived human induced pluripotent stem cells (hiPSC-LMNs) with FUS-H517D and in the post-mortem spinal cord of patients with ALS. RNA sequence analysis revealed that most nuclear lamina and nucleoporin-linking genes were significantly decreased in FUS-H517D hiPSC-LMNs.<\/jats:p>\n               <jats:p>This evidence suggests that disruption of the nuclear lamina and nucleoporins is crucial for ALS pathomechanisms. Combined with patient-derived hiPSC-LMNs and autopsy samples, this mouse model might provide a more reliable understanding of ALS pathogenesis and might aid in the development of therapeutic strategies.<\/jats:p>","DOI":"10.1093\/brain\/awae224","type":"journal-article","created":{"date-parts":[[2024,9,23]],"date-time":"2024-09-23T17:02:20Z","timestamp":1727110940000},"page":"3933-3948","source":"Crossref","is-referenced-by-count":9,"title":["Multiple lines of evidence for disruption of nuclear lamina and nucleoporins in FUS amyotrophic lateral sclerosis"],"prefix":"10.1093","volume":"147","author":[{"given":"Kensuke","family":"Okada","sequence":"first","affiliation":[{"name":"Department of Neurology, Keio University School of Medicine , Tokyo 160-8582 ,","place":["Japan"]},{"name":"Department of Physiology, Keio University School of Medicine , Tokyo 160-8582 ,","place":["Japan"]},{"name":"Keio University iPS Cell Research Center for Intractable Neurological Diseases (KiND), Keio 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