Fig. 4From: Humanized APOE genotypes influence lifespan independently of tau aggregation in the P301S mouse model of tauopathyUnbiased transcriptomic analysis of PS19 mice homozygous for APOE4 shows predominant immune signature. Brains of paralyzed PS/E4H mice and 9–10-month-old E4H mice were analyzed by RNAseq. Genes (A), cell types (B), astrocyte gene expression profiles (B) and aging/AD-associated profiles (B) differentially regulated in PS/E4H mice relative to E4H mice is shown. p values adjusted for multiple testing; FDR = 0.05. 1-way Anova. qval denotes false discovery rate. The enriched up- and down-regulated genes were plotted onto pathways using the GO database (C) and KEGG pathway database (D) and represented in bubble plots. Pathways with an over-represented p-value ≤ 0.05, the number of module genes within the pathway > 15 and an enrichment score > 1.5 are depicted. The bubble plots are colored by p-value and sized by the enrichment score. Size, number of genes within each module; ES, Enrichment Score; q value, false discovery rate. N = 4 mice for PS/E4H and 3 mice for E4HBack to article page