HCSGD entry for SOD1


1. General information

Official gene symbolSOD1
Entrez ID6647
Gene full namesuperoxide dismutase 1, soluble
Other gene symbolsALS ALS1 IPOA SOD hSod1 homodimer
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000187Activation of MAPK activityISSbiological_process
GO:0000303Response to superoxideIDAbiological_process
GO:0001541Ovarian follicle developmentISSbiological_process
GO:0001819Positive regulation of cytokine productionIDAbiological_process
GO:0001890Placenta developmentNASbiological_process
GO:0001895Retina homeostasisISSbiological_process
GO:0001975Response to amphetamineIEAbiological_process
GO:0002262Myeloid cell homeostasisISSbiological_process
GO:0002576Platelet degranulationTASbiological_process
GO:0004784Superoxide dismutase activityIDA IEAmolecular_function
GO:0005507Copper ion bindingIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005576Extracellular regionTAScellular_component
GO:0005615Extracellular spaceIDAcellular_component
GO:0005634NucleusIDAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005739MitochondrionIDAcellular_component
GO:0005759Mitochondrial matrixNAScellular_component
GO:0005777PeroxisomeIDA ISScellular_component
GO:0005829CytosolIDA TAScellular_component
GO:0005886Plasma membraneIDAcellular_component
GO:0006302Double-strand break repairISSbiological_process
GO:0006309Apoptotic DNA fragmentationISSbiological_process
GO:0006749Glutathione metabolic processISSbiological_process
GO:0006801Superoxide metabolic processIDA IEA ISSbiological_process
GO:0006879Cellular iron ion homeostasisISSbiological_process
GO:0007283SpermatogenesisISSbiological_process
GO:0007566Embryo implantationISS NASbiological_process
GO:0007569Cell agingIMPbiological_process
GO:0007596Blood coagulationTASbiological_process
GO:0007605Sensory perception of soundISSbiological_process
GO:0007626Locomotory behaviorISSbiological_process
GO:0008089Anterograde axon cargo transportISSbiological_process
GO:0008090Retrograde axon cargo transportISSbiological_process
GO:0008217Regulation of blood pressureISSbiological_process
GO:0008270Zinc ion bindingIDAmolecular_function
GO:0009408Response to heatISSbiological_process
GO:0010033Response to organic substanceIDAbiological_process
GO:0019226Transmission of nerve impulseISSbiological_process
GO:0019430Removal of superoxide radicalsIBA ISSbiological_process
GO:0030168Platelet activationTASbiological_process
GO:0030346Protein phosphatase 2B bindingIDAmolecular_function
GO:0031012Extracellular matrixIDAcellular_component
GO:0031410Cytoplasmic vesicleIDAcellular_component
GO:0031667Response to nutrient levelsIEAbiological_process
GO:0032287Peripheral nervous system myelin maintenanceISSbiological_process
GO:0032314Regulation of Rac GTPase activityIDAbiological_process
GO:0032839Dendrite cytoplasmIDAcellular_component
GO:0032930Positive regulation of superoxide anion generationIDAbiological_process
GO:0033081Regulation of T cell differentiation in thymusNASbiological_process
GO:0040014Regulation of multicellular organism growthISSbiological_process
GO:0042493Response to drugISSbiological_process
GO:0042542Response to hydrogen peroxideISSbiological_process
GO:0042554Superoxide anion generationIEAbiological_process
GO:0042802Identical protein bindingIPImolecular_function
GO:0042803Protein homodimerization activityNASmolecular_function
GO:0043025Neuronal cell bodyIDAcellular_component
GO:0043065Positive regulation of apoptotic processICbiological_process
GO:0043085Positive regulation of catalytic activityIDAbiological_process
GO:0043234Protein complexIDAcellular_component
GO:0043524Negative regulation of neuron apoptotic processISSbiological_process
GO:0045471Response to ethanolISSbiological_process
GO:0045541Negative regulation of cholesterol biosynthetic processIDAbiological_process
GO:0045859Regulation of protein kinase activityIDAbiological_process
GO:0046620Regulation of organ growthNASbiological_process
GO:0046688Response to copper ionIEAbiological_process
GO:0046716Muscle cell cellular homeostasisISSbiological_process
GO:0046872Metal ion bindingIEAmolecular_function
GO:0048365Rac GTPase bindingIDAmolecular_function
GO:0048538Thymus developmentNASbiological_process
GO:0048678Response to axon injuryISSbiological_process
GO:0050665Hydrogen peroxide biosynthetic processIDA ISSbiological_process
GO:0051087Chaperone bindingIPImolecular_function
GO:0051881Regulation of mitochondrial membrane potentialIMPbiological_process
GO:0060047Heart contractionIDAbiological_process
GO:0060052Neurofilament cytoskeleton organizationISSbiological_process
GO:0060087Relaxation of vascular smooth muscleISSbiological_process
GO:0060088Auditory receptor cell stereocilium organizationISSbiological_process
GO:0072593Reactive oxygen species metabolic processIDAbiological_process
GO:1902177Positive regulation of intrinsic apoptotic signaling pathway in response to oxidative stressIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.85995868700.45624043540.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.2266161302
GSE13712_SHEARUp0.2060070490
GSE13712_STATICUp0.0968535033
GSE19018Up0.1671028104
GSE19899_A1Down-0.1783673251
GSE19899_A2Down-0.0953943007
PubMed_21979375_A1Down-0.0912624139
PubMed_21979375_A2Down-0.2096441662
GSE35957Down-0.1533521500
GSE36640Up0.2757203683
GSE54402Down-0.0758785065
GSE9593Up0.1390891418
GSE43922Down-0.2836611231
GSE24585Down-0.0740662024
GSE37065Down-0.0031555837
GSE28863_A1Down-0.1282544853
GSE28863_A2Down-0.0206590899
GSE28863_A3Down-0.2003161822
GSE28863_A4Up0.0546309025
GSE48662Down-0.0796564495

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Compound

Target

Confidence score

Uniprot

CHEMBL272641CHEMBL23549P00441
CHEMBL1672028CHEMBL23549P00441
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  • Drugs

Name

Drug

Accession number

S-Oxy CysteineDB03382 EXPT01041
ArimoclomolDB05025 -

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-377-3pMIMAT0000730MIRT000992Luciferase reporter assay//Western blotFunctional MTI18716028
hsa-miR-377-3pMIMAT0000730MIRT000992Luciferase reporter assay//Non-Functional MTI21203553
hsa-miR-378a-3pMIMAT0000732MIRT043913CLASHFunctional MTI (Weak)23622248
hsa-miR-197-3pMIMAT0000227MIRT048056CLASHFunctional MTI (Weak)23622248
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  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 19 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26794818RESULTS: Our findings showed that SOD1 and CCS-1 were significantly down-regulated in pre-senescent cells while CCS-1 and PRDX6 were up-regulated in senescent cells (p<0
26696133SOD II levels increased gradually, whereas the SOD I and III levels were biphasic during the experimental periods after PPKO treatment
25852816Using cultured fibroblasts with trisomy 21 (T21F), this study aimed to ascertain whether an imbalance exists in activities, mRNA, and protein expression of the antioxidant enzymes SOD1, SOD2, glutathione-peroxidase, and catalase during the cell replication process in vitro
25852816T21F had high SOD1 expression and activity which led to an interenzymatic imbalance in the antioxidant defense system, accentuated with replicative senescence
25839657Intracellular ROS levels were increased in hBM-MSCs; this was accompanied by a decrease in the expression of the antioxidant enzymes catalase and superoxide dismutase (SOD)1 and 2 and of phosphorylated forkhead box O1 (p-FOXO1) as well as an increase in the expression of p53 and p16, along with a reduction in differentiation potential
25839657When the antioxidant ascorbic acid was used to eliminate excess ROS, the levels of antioxidant enzymes (catalase, SOD1 and 2, p-FOXO1, and p53) were partly restored
25536029Chronic CI inhibition did not increase mitochondrial superoxide levels or cellular lipid peroxidation and was paralleled by a specific increase in SOD2/GR, whereas SOD1/CAT/Gpx1/Gpx2/Gpx5 levels remained unchanged
25274775Expression of a pathogenic mutation of SOD1 sensitizes aprataxin-deficient cells and mice to oxidative stress and triggers hallmarks of premature ageing
23702294TRF1 is a homodimer with roles governing DNA architecture and negatively regulating telomere length
23049256With an aim of reducing cellular senescence and oxidative stress in DPSCs, an intracellular delivery system for superoxide dismutase 1 (SOD1) was developed
23049256We conjugated SOD1 with a cell-penetrating peptide known as low-molecular weight protamine (LMWP), and investigated the effect of LMWP-SOD1 conjugates on hydrogen peroxide-induced cellular senescence and osteoblastic differentiation
21720015Mechanistically, we found that Rb1 could markedly increase intracellular superoxide dismutase (Cu/Zn SOD/SOD1) activity and decrease the malondialdehyde (MDA) level in H(2)O(2)-treated HUVECs, and suppress the generation of intracellular reactive oxygen species (ROS)
21562236The expression of antioxidant defense genes, such as glutathione peroxidase-1, Cu/Zn superoxide dismutase (Sod1), paraoxonase enzymes (Pon1, Pon2, and Pon3), were significantly lower in the liver of HF/C pups than in C/C pups
21538411The specific activities of zinc/copper (Zn/Cu)-superoxide dismutase (SOD-1) and manganese (Mn)-superoxide dismutase (SOD-2) were assayed in young passage 5 fibroblasts and in serially subcultured cells that were characterized as senescent at passages 15-35
21538411SOD-1 and SOD-2 activities did not significantly change in senescent and young cells cultured in either routine medium [minimum essential medium 1 (MEM1)], or in Zn, Cu and Mn supplemented medium (MEM2) containing normal human plasma levels of the cations
21538411SOD-1 and SOD-2 activities, however, underwent parallel progressive significant activity increases in senescent passage 20 and 25 cells, which peaked in value in passage 30 and 35 cells subcultured in supplemented medium (MEM3) containing triple human plasma levels of the cations
21538411We infer that it was only possible to significantly stimulate SOD-1 and SOD-2 activities in senescent MEM3 cultured cells enabling them to combat oxidative stress
20812868S-Nitrosylation of protein-disulfide isomerase may also be associated with mutant Cu/Zn superoxide dismutase toxicity in amyotrophic lateral sclerosis
20528770In contrast, up-regulation of Nuak2 (NUAK family, SNF1-like kinase 2) and down-regulation of Lonp2 (Lon peptidase 2), Foxo3a (forkhead box O3a), Sod1 (copper/zinc superoxide dismutase) and Sesn1 (sestrin 1) in the kidneys of recuperated offspring suggest that protein homoeostasis and resistance to oxidative stress are compromised, leading to accelerated cellular senescence in these shorter-lived mice
16304208To begin to test this hypothesis, we compared the activities and steady-state mRNA and protein levels of the antioxidant enzymes copper zinc (CuZn) superoxide dismutase (CuZnSOD, SOD1), manganese (Mn) superoxide dismutase (MnSOD, SOD2), and glutathione peroxidase (GPx) and the levels of reduced and oxidized glutathione in Leydig cells isolated from the testes of young (4-month-old) and aged (20-month-old) Brown Norway rats
14732290Our previous data highlight the importance of antioxidant enzymes, superoxide dismutase 1 (Sod1) and glutathione peroxidase 1 (Gpx1), in regulating this process
14732290Previously, we demonstrated that a perturbation in the Sod1-to-Gpx1 ratio, as a consequence of Sod1 overexpression, leads to senescence-like changes
14732290We proposed that this was mediated via the Sod1 dismutation product H2O2, because H2O2 induced similar changes in control cells
14732290However, it has been suggested that H2O2 production, via Sod1 dismutation, is rate-limited by the availability of the substrate O2*-, and therefore age-related changes may occur as a result of other functions of Sod1
8824885Elevation in the ratio of Cu/Zn-superoxide dismutase to glutathione peroxidase activity induces features of cellular senescence and this effect is mediated by hydrogen peroxide
8824885In this study we investigate the effects of a perturbation in the ratio of Cu/Zn-superoxide dismutase activity (Sod1 dismutases
8824885Furthermore, fibroblasts established from individuals with Down syndrome have an increase in the ratio of Sod1 to Gpx1 activity compared with corresponding controls and senesce earlier
7492966Cu/Zn-superoxide dismutase and glutathione peroxidase during aging
7492966This is based on our observation that an altered Cu/Zn-superoxide dismutase (Sod1)/(Gpx1 plus Cat) ratio exists in the brain of aging mice and that this correlates with increased lipid damage
7492966Conversely, aging liver and kidney have an unaffected Sod1/(Gpx1 plus Cat) ratio and lipid damage is not increased with aging
7492966We also examine the Sod1 to Gpx1 ratio in Down syndrome tissue and show that all organs have an altered ratio
7492966Thus an altered Sod1/(Gpx1 plus Cat) ratio may also affect gene expression by altering the binding and/or availability of transcription factors to DNA
8777435The susceptibility reduction may not be ascribed to extracellular Asc2P or DehAsc, which was removed by aspirating and/or rinsing upon irradiation after the intracellular channelyzer analysis and dead cell-specific DNA-intercalator ethidium homodimer/fluorometry, respectively
8028395Intracellular Cu/Zn superoxide dismutase levels in T and non-T cells from normal aged subjects
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