A novel mouse model for-related muscular dystrophy with analysis of molecular pathogenesis and clinical phenotype.

Abstract

Our understanding of the molecular pathogenesis of-related muscular dystrophy (-MD) requires improving. Here, we report the phenotype, neuropathology, and transcriptomics data (scRNA-seq and bulk RNA-seq) of a newknockout mouse (dy/dy) which was created based on the human-MD mutation hotspot region using CRISPR-Cas9. The dy/dymice presented a severe phenotype with muscular dystrophy. Mouse brain scRNA-seq showed thatgene was expressed predominantly and specifically in vascular and leptomeningeal fibroblasts and vascular smooth muscle cells, and weakly in astrocytes in wild-type mouse. Laminin α2 expression on the cortical surface was observed with immunofluorescence. In dy/dy,expression was decreased in those cell types, which might be associated with the disruption of gliovascular basal lamina assembly. Additionally, transcriptomic investigation of muscles showed 2020 differentially expressed genes, mainly associated with the impaired muscle cytoskeleton and development. In summary, this study provided potentially useful information for understanding the molecular pathogenesis of-MD.