HCSGD entry for ARNTL


1. General information

Official gene symbolARNTL
Entrez ID406
Gene full namearyl hydrocarbon receptor nuclear translocator-like
Other gene symbolsBMAL1 BMAL1c JAP3 MOP3 PASD3 TIC bHLHe5
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000060Protein import into nucleus, translocationIEAbiological_process
GO:0000982RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activityIEA ISSmolecular_function
GO:0001047Core promoter bindingISSmolecular_function
GO:0001190RNA polymerase II transcription factor binding transcription factor activity involved in positive regulation of transcriptionIEAmolecular_function
GO:0003677DNA bindingIEA IGImolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIEAmolecular_function
GO:0004871Signal transducer activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005667Transcription factor complexIEA IPIcellular_component
GO:0005737CytoplasmIEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedISSbiological_process
GO:0006366Transcription from RNA polymerase II promoterISSbiological_process
GO:0007623Circadian rhythmTASbiological_process
GO:0016604Nuclear bodyIEAcellular_component
GO:0017162Aryl hydrocarbon receptor bindingIPImolecular_function
GO:0032922Circadian regulation of gene expressionIEA ISSbiological_process
GO:0042176Regulation of protein catabolic processIEAbiological_process
GO:0043425BHLH transcription factor bindingIEAmolecular_function
GO:0045944Positive regulation of transcription from RNA polymerase II promoterIDA IGIbiological_process
GO:0046982Protein heterodimerization activityIEAmolecular_function
GO:0046983Protein dimerization activityIEAmolecular_function
GO:0051879Hsp90 protein bindingIDAmolecular_function
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.07486066260.51386533570.57978446601.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.2642126714
GSE13712_SHEARUp0.2284905236
GSE13712_STATICDown-0.1498152098
GSE19018Down-0.2888956647
GSE19899_A1Up0.0673456780
GSE19899_A2Up0.5771370055
PubMed_21979375_A1Up0.4557689308
PubMed_21979375_A2Up0.3446202010
GSE35957Down-0.5423467878
GSE36640Down-0.6864232108
GSE54402Up0.3419962244
GSE9593Down-0.2902997000
GSE43922Up0.8359541145
GSE24585Up0.4642997788
GSE37065Up0.3929612482
GSE28863_A1Down-0.1235358097
GSE28863_A2Up0.1842765413
GSE28863_A3Down-0.3978112777
GSE28863_A4Down-0.0094084757
GSE48662Down-0.1695740656

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-494-3pMIMAT0002816MIRT006653Luciferase reporter assay//qRT-PCRFunctional MTI21799909
hsa-miR-142-3pMIMAT0000434MIRT006654Luciferase reporter assay//qRT-PCRFunctional MTI21799909
hsa-miR-142-3pMIMAT0000434MIRT006654Luciferase reporter assayFunctional MTI22958478
hsa-miR-142-3pMIMAT0000434MIRT006654MicroarrayFunctional MTI (Weak)17612493
hsa-miR-335-5pMIMAT0000765MIRT018183MicroarrayFunctional MTI (Weak)18185580
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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: 6 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26961881In contrast, mouse embryonic fibroblasts prepared from mice deficient in positive circadian clock regulators, Bmal1 or Clock, showed resistance to oncogene-induced transformation
26361874The key nuclear receptors and transcription factors REV-ERBalpha and RORalpha regulate Bmal1 expression and provide stability to the oscillator
26361874The deacetylase Sirtuin 1 (SIRT1) regulates the timing of the clock through acetylation of BMAL1 and PER2 and controls the clock-dependent functions, which can also be affected by environmental stressors
26199639Bavachalcone Enhances RORalpha Expression, Controls Bmal1 Circadian Transcription, and Depresses Cellular Senescence in Human Endothelial Cells
26199639In addition, bavachalcone induced RORalpha1 expression in mRNA and protein levels in a dose-dependent manner and enhanced the circadian amplitude of Bmal1 mRNA expression after serum shock
25938935Stress-mediated post-translational modification of molecular clock proteins, brain and muscle aryl hydrocarbon receptor nuclear translocator-like 1 (BMAL1) and PERIOD 2, is associated with a reduction in the activity/level of the deacetylase sirtuin 1 (SIRT1)
25938935Similarly, the levels of the nuclear receptor REV-ERBalpha and retinoic acid receptor-related orphan receptor alpha (ROR alpha), critical regulators of Bmal1 expression, are altered by environmental stresses
22457671Age-related BMAL1 change affects mouse bone marrow stromal cell proliferation and osteo-differentiation potential
22457671Due to recent research's indication that a core circadian component, brain and muscle ARNT-like 1 protein (BMAL1), has a role in premature aging, we investigated the normal aging mechanism in mice with their MSCs and Bmal1 gene/protein level
22457671Bmal1 gene and protein level were detected in these cells
22457671RESULTS: Bmal1 gene and protein level as well as S-phase fraction of the cell cycle decreased in MSCs along with the aging process
22457671CONCLUSIONS: These findings demonstrate that mouse MSCs changed with their proliferation and osteo-differentiation abilities at different aging stages, and that Bmal1 is related to the normal aging process in MSCs
22101268Deficiency of the circadian clock transcriptional factor BMAL1 results in the development of premature aging in mice
22101268In agreement with the accelerated aging phenotype, we observed an increase in the number of senescent cells in different tissues (lungs, liver and spleen) of Bmal1(-/-) mice, which suggests the important role of BMAL1 in the control of senescence in vivo
22101268However, no difference in the rate of proliferation and senescence between primary fibroblasts isolated from wild-type and Bmal1(-/-) mice has been detected, suggesting that BMAL1 does not play a significant role in replicative senescence in vitro
22101268BMAL1 deficient fibroblasts had an increased sensitivity to hydrogen peroxide treatment, and reduced sensitivity to DNA damaging anticancer drugs etoposide and daunorubicin
22101268We propose that BMAL1 is important for the regulation of oxidative stress and DNA damage responses, while deregulation of these processes upon BMAL1 deficiency leads to development of stress induced senescence in vivo
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