Figure 5.

snRNA-seq analysis of cells in iNgly1 −/− mouse cerebellum. (A) Experimental workflow of snRNA-seq of 8-wk-old Ngly1fl/fl, iNgly1−/−, and iNgly1−/−Sting1−/− mouse cerebella (n = 2 mice per genotype). (B) UMAP plot of all cells from iNgly1−/−, iNgly1−/−Sting1−/−, and Ngly1fl/fl mouse cerebella. (C) Dot plots of cell type–specific marker genes. (D and E) Dot plots of proteasome subunit and autophagy/mitophagy-related genes in Ngly1fl/fl, iNgly1−/−, and iNgly1−/−Sting1−/− Purkinje cells. (F) Pathway enrichment analysis of DEGs between Ngly1fl/fl and iNgly1−/− Bergmann glia. (G) Dot plots of cholesterol metabolism–related genes in Ngly1fl/fl, iNgly1−/−, and iNgly1−/−Sting1−/− Bergmann glia. (H) UMAP plot of granule cell subcluster from Ngly1fl/fl, iNgly1−/−, or iNgly1−/−Sting1−/− mouse cerebella. (I) Quantification of three genotypes in each granule cell subcluster. (J) Dot plots of hallmark gene expression in GC1 and GC2 subclusters. UMAP, Uniform Manifold Approximation and Projection.

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