HCSGD entry for ATF3


1. General information

Official gene symbolATF3
Entrez ID467
Gene full nameactivating transcription factor 3
Other gene symbols
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:0003700Sequence-specific DNA binding transcription factor activityIEAmolecular_function
GO:0003714Transcription corepressor activityTASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005730NucleolusIDAcellular_component
GO:0006094GluconeogenesisIEAbiological_process
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006987Activation of signaling protein activity involved in unfolded protein responseTASbiological_process
GO:0008284Positive regulation of cell proliferationIEAbiological_process
GO:0030968Endoplasmic reticulum unfolded protein responseTASbiological_process
GO:0035914Skeletal muscle cell differentiationIEAbiological_process
GO:0042802Identical protein bindingIPImolecular_function
GO:0043565Sequence-specific DNA bindingIEAmolecular_function
GO:0044267Cellular protein metabolic processTASbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.02333751380.55560258730.36274490881.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.3429243455
GSE13712_SHEARUp1.3404391348
GSE13712_STATICUp0.8481297742
GSE19018Up0.1800902011
GSE19899_A1Up0.2879317790
GSE19899_A2Up0.1405342549
PubMed_21979375_A1Up0.3974197252
PubMed_21979375_A2Up0.5714231234
GSE35957Down-0.5606435568
GSE36640Up0.7974139805
GSE54402Down-0.2060415196
GSE9593Up1.2298539697
GSE43922Down-0.0631717056
GSE24585Down-0.3566565783
GSE37065Up0.2393221286
GSE28863_A1Down-0.3559903191
GSE28863_A2Up0.2586426244
GSE28863_A3Down-0.0754819186
GSE28863_A4Up0.1991796376
GSE48662Down-0.0634943030

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

  • MicroRNAs

  • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-26b-5pMIMAT0000083MIRT029081MicroarrayFunctional MTI (Weak)19088304
hsa-miR-331-3pMIMAT0000760MIRT043494CLASHFunctional MTI (Weak)23622248
hsa-miR-17-5pMIMAT0000070MIRT050819CLASHFunctional 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: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25531190Activating transcription factor 3 (ATF3) plays a pleiotropic role in biological processes through genotoxic stress
25531190In this study, we examined the effects of acrylamide (ACR), a genotoxic carcinogen, on cellular senescence and the molecular mechanisms of ATF3 function in macrophages
25531190In addition, ACR treatment for 1, 3, or 5 days showed a concentration-dependent increase in ATF3 expression and G0/G1 phase arrest
25531190To better understand the role of ATF3 in controlling the senescence response to ACR, SA-beta-gal activity was examined using ATF3 knockdown and overexpression
25531190ACR-mediated senescence was significantly decreased by knockdown of ATF3, whereas it was increased with ATF3 overexpression
25531190We found that ATF3 regulated p53 and p21 levels
25531190ATF3 also played an important role in regulating intracellular reactive oxygen species (ROS) production in response to ACR treatment
21406393The underlying mechanism involves interruption of a double negative regulatory axis, whereby calcineurin and nuclear factors of activated T-cell signaling inhibits expression of ATF3, a negative regulator of p53
20485437Opposing roles for calcineurin and ATF3 in squamous skin cancer
20485437ATF3, a member of the 'enlarged' AP-1 family, is selectively induced by calcineurin/NFAT inhibition, both under experimental conditions and in clinically occurring tumours, and increased ATF3 expression accounts for suppression of p53-dependent senescence and enhanced tumorigenic potential
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