Table 3.
Top annotated GO, KEGG and IPA pathways in the SC of BAC-ATXN2-Q72 mice versus wild-type and −log10(P-value) for the indicated comparisons. Benjamini probabilities corrected for multiple pairwise comparisons were calculated for GO and KEGG terms (if significance was not achieved, uncorrected probabilities are shown, indicated by asterisks)
GO | KEGG | IPA | |||
---|---|---|---|---|---|
TG versus WT (untreated) | |||||
Glial cell development | 5.41 | Cholesterol metabolism | 3.16 | Hepatic fibrosis/hepatic stellate cell activation | 5.19 |
Glial cell differentiation | 5.19 | Herpes simplex infection | 1.65 | Interferon signaling | 4.74 |
Ensheathment of neurons | 4.57 | LXR/RXR activation | 4.68 | ||
Axon ensheathment | 4.57 | Th2 pathway | 3.99 | ||
Gliogenesis | 4.57 | Th1 and Th2 activation pathway | 3.88 | ||
Fatty acid biosynthetic process | 4.57 | ||||
TG-SAL versus WT-SAL | |||||
Lipid metabolic process | 9.02 | Steroid biosynthesis | 2.07 | Superpathway of cholesterol biosynthesis | 9.19 |
Fatty acid biosynthetic process | 5.97 | Fatty acid metabolism | 1.98 | Cholesterol biosynthesis I | 7.20 |
Sterol biosynthetic process | 4.82 | Biosynthesis of unsaturated fatty acids | 1.89 | Cholesterol biosynthesis II (via 24,25-dihydrolanosterol) | 7.20 |
Steroid metabolic process | 3.63 | Biosynthesis of antibiotics | 1.85 | Cholesterol biosynthesis III (via desmosterol) | 7.20 |
Unsaturated fatty acid biosynthetic process | 2.65 | Hepatic fibrosis/hepatic stellate cell activation | 4.93 | ||
Yellow module | |||||
Ion transport | 4.29* | Biosynthesis of unsaturated fatty acids | 3.12* | Tryptophan degradation X (mammalian via tryptamine) | 3.75 |
Fatty acid biosynthetic process | 3.94* | Nitrogen metabolism | 2.99* | Putrescine degradation III | 2.85 |
Aging | 3.80* | Chemical carcinogenesis | 2.41* | Th2 pathway | 2.76 |
Adult locomotory behavior | 3.42* | Neuroactive ligand–receptor interaction | 2.25* | Oleate biosynthesis II (animals) | 2.60 |
Unsaturated fatty acid biosynthetic process | 3.33* | Metabolism of xenobiotics by cytochrome P450 | 2.08* | Hepatic fibrosis/hepatic stellate cell activation | 2.56 |
Lightgreen module | |||||
Sterol biosynthetic process | 5.39 | Steroid biosynthesis | 3.07 | Superpathway of cholesterol biosynthesis | 10.50 |
Lipid metabolic process | 2.74 | Biosynthesis of antibiotics | 1.92 | Cholesterol biosynthesis I | 8.31 |
Cholesterol biosynthetic process | 2.73 | Neuroactive ligand–receptor interaction | 1.80 | Cholesterol biosynthesis II (via 24,25-dihydrolanosterol) | 8.31 |
Steroid metabolic process | 2.63 | Cholesterol biosynthesis III (via desmosterol) | 8.31 | ||
Steroid biosynthetic process | 2.18 | Zymosterol biosynthesis | 4.46 | ||
Midnightblue module | |||||
Defense response to virus | 26.81 | Herpes simplex infection | 7.49 | Interferon signaling | 13.20 |
Immune system process | 22.69 | Influenza A | 6.49 | Activation of IRF by cytosolic pattern recognition receptors | 12.40 |
Innate immune response | 19.78 | Measles | 6.51 | Antigen presentation pathway | 7.63 |
Response to virus | 17.48 | Hepatitis C | 5.47 | Role of RIG1-like receptors in antiviral innate immunity | 5.70 |
Cellular response to interferon-beta | 17.16 | RIG-I-like receptor signaling pathway | 2.94 | Role of pattern recognition receptors in recognition of bacteria and viruses | 5.40 |