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. 2022 Nov 28;30(2):369–382. doi: 10.1038/s41418-022-01089-7

Fig. 1. The association between ALS, ferroptosis, and SPY1 is uncovered in the transcriptome data of primary rat neurons.

Fig. 1

The transcriptome data of GSE7493 abstracted from embryonic MNs in the SOD1G93A mutant model of ALS was downloaded for analysis. A Standardization with log2 for the data, including 4 wildtypes (WT) and 5 mutants (MU). B GSEA for ferroptosis in MU vs WT (NES = 1.26, p = 0.046). C Differential expression analysis in MU vs WT containing 193 up-regulated genes and 224 down-regulated genes (p < 0.05, |logFC | ≥ 1). D The data were divided into groups of 4 lows and 4 highs based on the expression of SPY1. The heatmap exhibited the top 20 DEGs in SPY1 High vs. Low (p < 0.05, |logFC | ≥ 1). E The Venn diagram overlapped 417 DEGs in MU vs. WT, 420 DEGs in SPY1 High vs. Low, and 259 ferroptosis-related genes. F DEGs in SPY1 High vs Low were performed enrichment in the GO terms of CC, BP, and MF via David. The bar chart showed the top 5 of each term sorted by gene ratio (p < 0.05). G Pearson correlation analysis was performed on the expression of SPY1 and GCH1 (r = 0.7387, p = 0.0230). Statistical analysis by Student’s t-test.