HCSGD entry for CSNK2A1


1. General information

Official gene symbolCSNK2A1
Entrez ID1457
Gene full namecasein kinase 2, alpha 1 polypeptide
Other gene symbolsCK2A1 CKII CSNK2A3
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:0000278Mitotic cell cycleTASbiological_process
GO:0004674Protein serine/threonine kinase activityIDA IEA TASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005524ATP bindingIEAmolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005829CytosolTAScellular_component
GO:0005886Plasma membraneTAScellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedIEAbiological_process
GO:0006468Protein phosphorylationIDAbiological_process
GO:0007165Signal transductionTASbiological_process
GO:0007411Axon guidanceTASbiological_process
GO:0008284Positive regulation of cell proliferationIDAbiological_process
GO:0016055Wnt signaling pathwayIEAbiological_process
GO:0016580Sin3 complexIDAcellular_component
GO:0016581NuRD complexIDAcellular_component
GO:0030177Positive regulation of Wnt signaling pathwayIMPbiological_process
GO:0030307Positive regulation of cell growthIDAbiological_process
GO:0031519PcG protein complexIDAcellular_component
GO:0043154Negative regulation of cysteine-type endopeptidase activity involved in apoptotic processIMPbiological_process
GO:0045732Positive regulation of protein catabolic processIDAbiological_process
GO:0047485Protein N-terminus bindingIPImolecular_function
GO:0051879Hsp90 protein bindingTASmolecular_function
GO:0061077Chaperone-mediated protein foldingTASbiological_process
GO:0071174Mitotic spindle checkpointIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.07432516620.98119836250.57869089301.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.2414372533
GSE13712_SHEARDown-0.0310075147
GSE13712_STATICUp0.1130445686
GSE19018Up0.4131266302
GSE19899_A1Up0.3779443771
GSE19899_A2Up0.6783744484
PubMed_21979375_A1Up0.4289074947
PubMed_21979375_A2Up0.0779009156
GSE35957Down-0.1053494119
GSE36640Down-0.1596388960
GSE54402Up0.3808538221
GSE9593Up0.2213117931
GSE43922--
GSE24585--
GSE37065--
GSE28863_A1Up0.2247039770
GSE28863_A2Up0.0388155888
GSE28863_A3Down-0.1388315083
GSE28863_A4Up0.0393427870
GSE48662Up0.0384273451

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

(5-Oxo-5,6-Dihydro-Indolo[1,2-a]Quinazolin-7-Yl)-Acetic AcidDB01765 EXPT01927
1,8-Di-Hydroxy-4-Nitro-Xanthen-9-OneDB02170 EXPT02205
1,8-Di-Hydroxy-4-Nitro-AnthraquinoneDB03035 EXPT01762
BenzamidineDB03127 EXPT00669
5,8-Di-Amino-1,4-Dihydroxy-AnthraquinoneDB03924 EXPT02206
Phosphoaminophosphonic Acid-Adenylate EsterDB04395 EXPT00524
Tetrabromo-2-BenzotriazoleDB04462 EXPT03020
DIMETHYL-(4,5,6,7-TETRABROMO-1H-BENZOIMIDAZOL-2-YL)-AMINEDB04719 -
S-METHYL-4,5,6,7-TETRABROMO-BENZIMIDAZOLEDB04720 -
N1,N2-ETHYLENE-2-METHYLAMINO-4,5,6,7-TETRABROMO-BENZIMIDAZOLEDB04721 -
3-METHYL-1,6,8-TRIHYDROXYANTHRAQUINONEDB07715 -
3,8-DIBROMO-7-HYDROXY-4-METHYL-2H-CHROMEN-2-ONEDB07802 -
19-(cyclopropylamino)-4,6,7,15-tetrahydro-5H-16,1-(azenometheno)-10,14-(metheno)pyrazolo[4,3-o][1,3,9]triazacyclohexadecin-8(9H)-oneDB08338 -
N,N'-DIPHENYLPYRAZOLO[1,5-A][1,3,5]TRIAZINE-2,4-DIAMINEDB08340 -
4-(2-(1H-IMIDAZOL-4-YL)ETHYLAMINO)-2-(PHENYLAMINO)PYRAZOLO[1,5-A][1,3,5]TRIAZINE-8-CARBONITRILEDB08345 -
2-(CYCLOHEXYLMETHYLAMINO)-4-(PHENYLAMINO)PYRAZOLO[1,5-A][1,3,5]TRIAZINE-8-CARBONITRILEDB08353 -
2-(4-CHLOROBENZYLAMINO)-4-(PHENYLAMINO)PYRAZOLO[1,5-A][1,3,5]TRIAZINE-8-CARBONITRILEDB08354 -
2-(4-ETHYLPIPERAZIN-1-YL)-4-(PHENYLAMINO)PYRAZOLO[1,5-A][1,3,5]TRIAZINE-8-CARBONITRILEDB08360 -
N-(3-(8-CYANO-4-(PHENYLAMINO)PYRAZOLO[1,5-A][1,3,5]TRIAZIN-2-YLAMINO)PHENYL)ACETAMIDEDB08362 -
5,6-dichloro-1-beta-D-ribofuranosyl-1H-benzimidazoleDB08473 -
1,2,5,8-tetrahydroxyanthracene-9,10-dioneDB08660 -
Ellagic AcidDB08846 DB08468

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-216b-5pMIMAT0004959MIRT007207Immunoblot//Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23137536
hsa-miR-337-3pMIMAT0000754MIRT007208Immunoblot//Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23137536
hsa-miR-760MIMAT0004957MIRT007209Immunoblot//Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23137536
hsa-miR-186-5pMIMAT0000456MIRT007210Immunoblot//Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23137536
hsa-miR-22-3pMIMAT0000077MIRT030638SequencingFunctional MTI (Weak)20371350
hsa-miR-652-3pMIMAT0003322MIRT039530CLASHFunctional MTI (Weak)23622248
hsa-miR-615-3pMIMAT0003283MIRT039801CLASHFunctional MTI (Weak)23622248
hsa-miR-183-5pMIMAT0000261MIRT047136CLASHFunctional MTI (Weak)23622248
hsa-miR-10b-5pMIMAT0000254MIRT047431CLASHFunctional MTI (Weak)23622248
hsa-miR-10a-5pMIMAT0000253MIRT047540CLASHFunctional MTI (Weak)23622248
hsa-let-7c-5pMIMAT0000064MIRT051854CLASHFunctional MTI (Weak)23622248
hsa-let-7b-5pMIMAT0000063MIRT052272CLASHFunctional MTI (Weak)23622248
hsa-let-7a-5pMIMAT0000062MIRT052591CLASHFunctional 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: 11 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26703243Regulation of protein kinase CK2 catalytic activity by protein kinase C and phospholipase D2
25064843PLD2 overexpression increased protein kinase CK2 (also known as casein kinase 2) (CK2) activity
23768371An inhibitor of the protein kinase CKII (CKII) was purified from leaves of Glycine max (L
23768371Coumestrol inhibited the phosphotransferase activity of CKII toward beta-casein, with an IC50 of about 5 muM
23523798We previously reported that CKII downregulation induces senescence in human lung fibroblast IMR-90 and colon cancer HCT116 cells
23523798CKIIalpha knock-down or CKII inhibitor treatment strikingly increased phosphorylation of mTOR, p70S6K, an mTOR substrate, and AKT, whereas CKIIalpha overexpression reduced this phosphorylation event
23523798This result indicated that CKII inhibition activated the PI3K-AKT-mTOR pathway
23137536MiR-186, miR-216b, miR-337-3p, and miR-760 cooperatively induce cellular senescence by targeting alpha subunit of protein kinase CKII in human colorectal cancer cells
23137536To investigate the role of microRNAs (miRNAs) in CKII downregulation during senescence, we employed computational algorithms
21968188Here, CKII inhibition induced acetylation of p53 at K382 in HCT116 and HEK293 cells
21968188CKII inhibition reduced SIRT1 activity in cells
21968188CKII phosphorylated and activated human SIRT1 in vitro
21968188These results reveal that CKII downregulation induces p53 stabilization by negatively regulating SIRT1 deacetylase activity during senescence
21702981BACKGROUND: Protein kinase CK2 is a highly conserved, ubiquitous protein serine/threonine kinase that phosphorylates many substrates and has a global role in numerous biological and pathological processes
19855935The p53-p21(Cip1/WAF1) pathway is necessary for cellular senescence induced by the inhibition of protein kinase CKII in human colon cancer cells
19855935We have previously shown that the down-regulation of protein kinase CKII activity is tightly associated with cellular senescence of human fibroblast IMR-90 cells
19855935A senescent marker appeared after staining for senescence-associated beta-galactosidase activity in wild-type HCT116 cells treated with CKII inhibitor or CKIIalpha siRNA, but this response was almost abolished in p53- or p21(Cip1/WAF1)-null cells
19855935Increased cellular levels of p53 and p21(Cip1/WAF1) protein occurred with the inhibition of CKII
19855935CKII inhibition upregulated p53 and p21(Cip1/WAF1) expression at post-transcriptional level and transcription level, respectively
19855935RB phosphorylation significantly decreased in cells treated with CKII inhibitor
19855935Taken together, this study shows that the activation of the p53-p21(Cip1/WAF1) pathway acts as a major mediator of cellular senescence induced by CKII inhibition
19826041Protein kinase CK2 regulates cytoskeletal reorganization during ionizing radiation-induced senescence of human mesenchymal stem cells
19027835Silencing of the CKII alpha and CKII alpha' genes during cellular senescence is mediated by DNA methylation
19027835Previously we reported that down-regulation of CKII activity is tightly associated with cellular senescence and that the mRNA and protein levels of CKII alpha decrease during senescence
19027835The present study demonstrates that the mRNA and protein levels of CKII alpha' also decrease during senescence
19027835Knockdown of CKII alpha' in IMR-90 cells by RNA interference induced the senescent phenotype
19027835However, bisulfite sequencing analysis revealed that the methylation status of the CpG islands within the reported CKII alpha and CKII alpha' promoters was not associated with senescence
19027835Instead, senescence-dependent hypermethylation was observed in the region ranging from position +1112 to +1128 of the CKII alpha gene and at positions -527 and +829 of the CKII alpha' gene
16442104Downregulation of protein kinase CKII is associated with cellular senescence
16442104Protein kinase CKII (CKII) plays a critical role in cell growth and proliferation
16442104In this study, we examine how CKII activity is regulated during cellular senescence
16442104Our results demonstrate that CKII activity apparently decreases during both replicative and H2O2-induced senescence in human diploid fibroblast IMR-90 cells
16442104Treatment of IMR-90 cells with CKII inhibitors 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole and apigenin led cells to acquire a senescent phenotype as judged by the senescence-associated beta-galactosidase marker and overexpression of p53 and p21(Waf-1)
16442104In parallel, CKII activity was transcriptional downregulated in rat liver and testis with advancing age
16442104Taken together, these results suggest that downregulation of CKII activity is tightly associated not only with cellular senescence but also with organism aging
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