HCSGD entry for APEX1
1. General information
Official gene symbol | APEX1 |
---|---|
Entrez ID | 328 |
Gene full name | APEX nuclease (multifunctional DNA repair enzyme) 1 |
Other gene symbols | APE APE1 APEN APEX APX HAP1 REF1 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000737 | DNA catabolic process, endonucleolytic | IDA TAS | biological_process |
GO:0003677 | DNA binding | IDA IEA | molecular_function |
GO:0003684 | Damaged DNA binding | IDA | molecular_function |
GO:0003713 | Transcription coactivator activity | IDA | molecular_function |
GO:0003714 | Transcription corepressor activity | TAS | molecular_function |
GO:0003723 | RNA binding | IEA | molecular_function |
GO:0003906 | DNA-(apurinic or apyrimidinic site) lyase activity | IDA TAS | molecular_function |
GO:0004519 | Endonuclease activity | IDA IEA | molecular_function |
GO:0004520 | Endodeoxyribonuclease activity | TAS | molecular_function |
GO:0004521 | Endoribonuclease activity | IEA | molecular_function |
GO:0004523 | RNA-DNA hybrid ribonuclease activity | TAS | molecular_function |
GO:0004528 | Phosphodiesterase I activity | TAS | molecular_function |
GO:0004844 | Uracil DNA N-glycosylase activity | TAS | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005622 | Intracellular | IEA | cellular_component |
GO:0005634 | Nucleus | IDA IEA | cellular_component |
GO:0005654 | Nucleoplasm | IDA TAS | cellular_component |
GO:0005667 | Transcription factor complex | IEA | cellular_component |
GO:0005730 | Nucleolus | IDA | cellular_component |
GO:0005737 | Cytoplasm | IDA | cellular_component |
GO:0005739 | Mitochondrion | IDA IEA | cellular_component |
GO:0005783 | Endoplasmic reticulum | TAS | cellular_component |
GO:0005813 | Centrosome | IDA | cellular_component |
GO:0005840 | Ribosome | TAS | cellular_component |
GO:0006281 | DNA repair | IDA IEA TAS | biological_process |
GO:0006284 | Base-excision repair | TAS | biological_process |
GO:0006308 | DNA catabolic process | IDA TAS | biological_process |
GO:0006310 | DNA recombination | IEA | biological_process |
GO:0006351 | Transcription, DNA-templated | IEA | biological_process |
GO:0006355 | Regulation of transcription, DNA-templated | IEA | biological_process |
GO:0007568 | Aging | IEA | biological_process |
GO:0008081 | Phosphoric diester hydrolase activity | IDA | molecular_function |
GO:0008408 | 3'-5' exonuclease activity | IDA TAS | molecular_function |
GO:0014912 | Negative regulation of smooth muscle cell migration | IEA | biological_process |
GO:0016491 | Oxidoreductase activity | IDA | molecular_function |
GO:0016607 | Nuclear speck | IDA | cellular_component |
GO:0016890 | Site-specific endodeoxyribonuclease activity, specific for altered base | IDA | molecular_function |
GO:0031490 | Chromatin DNA binding | IDA | molecular_function |
GO:0032403 | Protein complex binding | IEA | molecular_function |
GO:0042493 | Response to drug | IEA | biological_process |
GO:0043488 | Regulation of mRNA stability | IMP | biological_process |
GO:0045454 | Cell redox homeostasis | IEA | biological_process |
GO:0045739 | Positive regulation of DNA repair | IDA | biological_process |
GO:0046872 | Metal ion binding | IDA | molecular_function |
GO:0048471 | Perinuclear region of cytoplasm | IDA | cellular_component |
GO:0051059 | NF-kappaB binding | IEA | molecular_function |
GO:0055114 | Oxidation-reduction process | IDA | biological_process |
GO:0070301 | Cellular response to hydrogen peroxide | IEA | biological_process |
GO:0071320 | Cellular response to cAMP | IEA | biological_process |
GO:0071375 | Cellular response to peptide hormone stimulus | IEA | biological_process |
GO:0080111 | DNA demethylation | IDA | biological_process |
GO:0090305 | Nucleic acid phosphodiester bond hydrolysis | IDA TAS | biological_process |
GO:0090501 | RNA phosphodiester bond hydrolysis | TAS | biological_process |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | TAS | biological_process |
GO:1900087 | Positive regulation of G1/S transition of mitotic cell cycle | IEA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.8854125223 | 0.0181252764 | 0.9999902473 | 0.2633632450 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.7324856837 |
GSE13712_SHEAR | Down | -0.4765475868 |
GSE13712_STATIC | Down | -0.3870861474 |
GSE19018 | Down | -0.7688162087 |
GSE19899_A1 | Down | -0.7736736802 |
GSE19899_A2 | Down | -0.3774167527 |
PubMed_21979375_A1 | Down | -0.7672099932 |
PubMed_21979375_A2 | Down | -0.4984468344 |
GSE35957 | Down | -0.3052349478 |
GSE36640 | Down | -0.6469229352 |
GSE54402 | Up | 0.1336399031 |
GSE9593 | Down | -0.1976323411 |
GSE43922 | Down | -0.3444698033 |
GSE24585 | Down | -0.1111248568 |
GSE37065 | Down | -0.1942498032 |
GSE28863_A1 | Down | -0.1007968638 |
GSE28863_A2 | Down | -0.0645705469 |
GSE28863_A3 | Up | 0.4833615867 |
GSE28863_A4 | Up | 0.3427808650 |
GSE48662 | Down | -0.3192612796 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
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- Drugs
Name | Drug | Accession number |
---|---|---|
Lucanthone | DB04967 | - |
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-935 | MIMAT0004978 | MIRT036701 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-185-5p | MIMAT0000455 | MIRT045386 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-100-5p | MIMAT0000098 | MIRT048405 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-99a-5p | MIMAT0000097 | MIRT048610 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-17-5p | MIMAT0000070 | MIRT050830 | CLASH | Functional 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: 5 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
27106773 | To evaluate the expression of markers correlated with cellular senescence and DNA damage (8-hydroxy-2'-deoxy-guanosine (8-OHdG), p53, p21, APE1/Ref-1 (APE1), interleukin (IL-6 and IL-8) in placentas from healthy and pathologic pregnancies |
27106773 | In this study, we demonstrated a significant influence of gestational age on the expression in the trophoblast of 8-OHdG, p53, p21, APE1, and IL-6 |
27106773 | In placentas of cases affected by PE, HELLP, or IUGR, there was an increased expression of 8-OHdG, p53, APE1, and IL-6 compared to controls (only IL-8 was significantly decreased in cases) |
27106773 | In both groups of pathology between 22- and 34-week gestation and after 34-week gestation, APE1 levels were higher in the trophoblast of women affected by hypertensive disorders of pregnancy than women carrying an IUGR fetus |
27106773 | Placentas from pathological pregnancies had an altered expression of 8-OHdG, p53, p21, APE1, IL-6, and IL-8 |
26224580 | Statins also impaired the expression of DNA repair genes, including XRCC4, XRCC6, and Apex1 |
25682875 | Structure/function analysis established that a single Cut repeat domain can stimulate the DNA binding, Schiff-base formation, glycosylase and AP-lyase activities of 8-oxoguanine DNA glycosylase 1, OGG1 |
25682875 | Strikingly and in contrast to previous reports, OGG1 exhibits efficient AP-lyase activity in the presence of a Cut repeat |
25363496 | Apurinic/apyrimidinic endonuclease 1 on aging-associated deteriorations in rat kidneys |
25363496 | We have reported a possible involvement of apurinic/apyrimidinic endonuclease 1 (APE1), one of the DNA repair pathways, in various nephropathy models and found that there is a close connection between APE1 and p53-dependent apoptosis |
25363496 | Western blot assay was compared for p53, bax, cleaved caspase 3, rH2AX, and APE1 |
25363496 | Immunohistochemical staining of 8-hydroxy-2'-deoxyguanosine (8-OHdG) and APE1 was performed |
25363496 | All the checked variables were significantly increased with aging: 1) increased p53, bax, and caspase 3 may activate the apoptotic pathway, 2) increased rH2AX and 8-OHdG immunolocalization in the proximal convoluted tubules might mean augmented DNA damage, and 3) increased APE1 might be caused by the immunoreactivity in the distal convoluted tubules while decreased in the proximal convoluted tubules |
25363496 | These results suggested that APE1 might have little protective effects on p53-dependent apoptosis irrespective of DNA repair activities in aged renal proximal tubules |
19492297 | Downregulation of APE1/Ref-1 is involved in the senescence of mesenchymal stem cells |
19492297 | Interestingly, even though endogenous superoxide increased in a replicative senescence model, the expression of APE1/Ref-1, which is sensitive to intracellular redox state, decreased |
19492297 | This change is related to the p53 activity that negatively regulates APE1/Ref-1 |
19492297 | Overexpression of APE1/Ref-1 suppressed superoxide production and decreased SA beta-gal in hBMSCs |
19492297 | In conclusion, intracellular superoxide accumulation appears to be the main cause of the senescence of hBMSCs, and overexpression of APE1/Ref-1 can rescue cells from the senescence phenotype |
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