HCSGD entry for CREB1


1. General information

Official gene symbolCREB1
Entrez ID1385
Gene full namecAMP responsive element binding protein 1
Other gene symbolsCREB
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000790Nuclear chromatinIEAcellular_component
GO:0000980RNA polymerase II distal enhancer sequence-specific DNA bindingIDAmolecular_function
GO:0001102RNA polymerase II activating transcription factor bindingIPImolecular_function
GO:0001190RNA polymerase II transcription factor binding transcription factor activity involved in positive regulation of transcriptionIDAmolecular_function
GO:0002224Toll-like receptor signaling pathwayTASbiological_process
GO:0002755MyD88-dependent toll-like receptor signaling pathwayTASbiological_process
GO:0002756MyD88-independent toll-like receptor signaling pathwayTASbiological_process
GO:0003677DNA bindingIEAmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDA IEAmolecular_function
GO:0003705RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activityIDAmolecular_function
GO:0003712Transcription cofactor activityTASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA IEAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005667Transcription factor complexIEAcellular_component
GO:0005719Nuclear euchromatinIDAcellular_component
GO:0005730NucleolusIDAcellular_component
GO:0006366Transcription from RNA polymerase II promoterIDAbiological_process
GO:0006468Protein phosphorylationIDAbiological_process
GO:0007165Signal transductionTASbiological_process
GO:0007173Epidermal growth factor receptor signaling pathwayTASbiological_process
GO:0007202Activation of phospholipase C activityTASbiological_process
GO:0007219Notch signaling pathwayTASbiological_process
GO:0007268Synaptic transmissionTASbiological_process
GO:0007409AxonogenesisIEAbiological_process
GO:0007411Axon guidanceTASbiological_process
GO:0007595LactationIEAbiological_process
GO:0008361Regulation of cell sizeIEAbiological_process
GO:0008543Fibroblast growth factor receptor signaling pathwayTASbiological_process
GO:0010033Response to organic substanceIDAbiological_process
GO:0010944Negative regulation of transcription by competitive promoter bindingIDAbiological_process
GO:0016032Viral processIEAbiological_process
GO:0021983Pituitary gland developmentIEAbiological_process
GO:0033363Secretory granule organizationIEAbiological_process
GO:0034134Toll-like receptor 2 signaling pathwayTASbiological_process
GO:0034138Toll-like receptor 3 signaling pathwayTASbiological_process
GO:0034142Toll-like receptor 4 signaling pathwayTASbiological_process
GO:0034146Toll-like receptor 5 signaling pathwayTASbiological_process
GO:0034162Toll-like receptor 9 signaling pathwayTASbiological_process
GO:0034166Toll-like receptor 10 signaling pathwayTASbiological_process
GO:0035497CAMP response element bindingIDAmolecular_function
GO:0035666TRIF-dependent toll-like receptor signaling pathwayTASbiological_process
GO:0038095Fc-epsilon receptor signaling pathwayTASbiological_process
GO:0038123Toll-like receptor TLR1:TLR2 signaling pathwayTASbiological_process
GO:0038124Toll-like receptor TLR6:TLR2 signaling pathwayTASbiological_process
GO:0040018Positive regulation of multicellular organism growthIEAbiological_process
GO:0042493Response to drugIEAbiological_process
GO:0043565Sequence-specific DNA bindingIEAmolecular_function
GO:0045087Innate immune responseTASbiological_process
GO:0045600Positive regulation of fat cell differentiationIEA ISSbiological_process
GO:0045672Positive regulation of osteoclast differentiationIEAbiological_process
GO:0045893Positive regulation of transcription, DNA-templatedISSbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterIDA IEAbiological_process
GO:0046887Positive regulation of hormone secretionIEAbiological_process
GO:0046889Positive regulation of lipid biosynthetic processIEA ISSbiological_process
GO:0048011Neurotrophin TRK receptor signaling pathwayTASbiological_process
GO:0048015Phosphatidylinositol-mediated signalingTASbiological_process
GO:0050821Protein stabilizationIEA ISSbiological_process
GO:0051403Stress-activated MAPK cascadeTASbiological_process
GO:0060430Lung saccule developmentIEAbiological_process
GO:0060509Type I pneumocyte differentiationIEAbiological_process
GO:0071363Cellular response to growth factor stimulusIEAbiological_process
Entries Per Page
Displaying Page of

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.93539629570.02777228070.99999024730.3171341432

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

Data sourceUp or downLog fold change
GSE11954Down-0.1775560637
GSE13712_SHEARUp0.0485642291
GSE13712_STATICDown-0.0987273646
GSE19018Down-0.1952239677
GSE19899_A1Down-0.3891519543
GSE19899_A2Down-0.6333886371
PubMed_21979375_A1Down-0.5740938136
PubMed_21979375_A2Down-0.9448529445
GSE35957Down-0.2069550887
GSE36640Down-0.8704594682
GSE54402Up0.1171278940
GSE9593Down-0.1241024466
GSE43922Down-0.3006298843
GSE24585Up0.3457937150
GSE37065Up0.1382555549
GSE28863_A1Up0.2974741674
GSE28863_A2Up0.3465966935
GSE28863_A3Down-0.7471555894
GSE28863_A4Down-0.3660491660
GSE48662Up0.1275091926

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Name

Drug

Accession number

NaloxoneDB01183 APRD00025

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-34b-5pMIMAT0000685MIRT000066Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI19258499
hsa-miR-34b-5pMIMAT0000685MIRT000066Luciferase reporter assayFunctional MTI19461653
hsa-miR-203aMIMAT0000264MIRT006496Luciferase reporter assay//qRT-PCRFunctional MTI21707582
hsa-miR-103a-3pMIMAT0000101MIRT004766Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI20886090
hsa-miR-182-5pMIMAT0000259MIRT006273GFP reporter assayFunctional MTI22325466
hsa-miR-200b-3pMIMAT0000318MIRT007342Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23543137
hsa-miR-200b-3pMIMAT0000318MIRT007342Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI23546867
hsa-miR-122-5pMIMAT0000421MIRT023389MicroarrayFunctional MTI (Weak)17612493
Entries Per Page
Displaying Page of
    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 8 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

26414604ALA stimulated cyclic adenosine monophosphate (cAMP) signaling, which in turn activated the cAMP response element-binding protein (CREB), a co-factor for PGC-1alpha expression
23991634Lung aging is associated with morphological and physiological changes in which alterations in transcription factors, including the cyclic adenosine monophosphate response element-binding protein (CREB), could play a role
23991634We studied CREB in lung tissue from mice at different ages and in response to known age-related factors (e
23991634Our study shows that protein but not mRNA levels of CREB are reduced in the lungs of old mice
23991634CREB reduction was also observed in senescent human lung fibroblasts (WI-38, LuFi) and human lung epithelial cells (A549) cultured on AGE-modified collagen matrix
23991634Reduction of CREB protein is partially based on pre- and posttranslational modifications as exhibited by an increase in the CREB-regulating microRNA 34b and CREB ubiquitination
23991634Permanent down-regulation of CREB in lung cells impaired cell proliferation and viability and increased the number of cells with senescence-associated beta-galactosidase activity
23991634CREB down-regulation was accompanied by the reduced expression of 165 genes in WI-38 fibroblasts and A549 epithelial cells, of which 15 genes showed a reduced expression in lung tissues of old mice
23991634Our data demonstrate that the reduced protein expression of CREB might play a significant role in lung aging by modifying the transcription of RAB27A, IGFBP3, and other target genes
21047255By following this methodological approach, we recently obtained data fitting a model in which, in response to chronic impairment of cellular bioenergetics imposed by metformin-induced mitochondrial uncoupling as assessed by the phosphorylation state of cAMP-response element binding protein (CREB), tumor cells can retrogress from a differentiated state to a more CD44(+) stem-like primitive state epigenetically governed by the Polycomb-group suppressor BMI1-a crucial "stemness" gene involved in the epigenetic maintenance of adult stem cells
20214903Role of CREB in the regulatory action of sarsasapogenin on muscarinic M1 receptor density during cell aging
20214903This work studied the role of cyclic AMP responsive element binding protein (CREB) in the up-regulation of M(1) muscarinic acetylcholine receptor (M(1) receptor) density by sarsasapogenin (ZMS) in CHO cells transfected with M(1) receptor gene (CHOm1 cells)
20214903During cell aging, sarsasapogenin elevated M(1) receptor density as well as CREB and phosphor-CREB (pCREB) levels
20214903CREB peaked earliest, followed by pCREB and M(1) receptor density peaked last
20214903When CREB synthesis was blocked by antisense oligonucleotides, the elevation effect of sarsasapogenin on M(1) receptor density was abolished
20214903These results suggest that sarsasapogenin up-regulates M(1) receptor density in aged cells by promoting CREB production and phosphorylation
20193693Gi-protein inhibitor, guanosine 5'-O-(2-thiodiphosphate), induces senescence-associated beta-galactosidase positive cell formation through CREB phosphorylation
20193693AIMS: We evaluated Gi-protein inhibitor, guanosine 5'-O-(2-thiodiphosphate)(GOT)-induced senescence-associated(SA)-beta-galactosidase(Gal) positive cell formation to determine if it occurred through phosphorylation of cyclic AMP-dependent response element binding protein (CREB)
20193693CREB phosphorylation and molecular changes were analyzed by western blot
20193693CREB phosphorylation increased in response to GOT treatment but then decreased over 24h
20193693SA-beta-Gal positive cell formation increased in response to transient transfection of pS6-RSV-CREB and no changes were detected following CREB knockdown with CREB-siRNA
20193693In addition, CREB phosphorylation was delayed by treatment with the anti-cellular senescence agents, clitocybins which also reduced the number of SA-beta-Gal positive cells
20193693Collectively, our data showed that GOT-induced CREB phosphorylation initiated SA-beta-Gal positive cell formation after which decreased in SA-beta-Gal positive cells
20193693SIGNIFICANCE: These findings suggest for the first time that CREB phosphorylation by GOT could induce cellular senescence as judged by SA-beta-Gal positive cell formation
16672767In attempts to define the molecular events associated with the age-dependent changes in cAMP profiles, we determined the protein kinase A (PKA) activity, phosphorylation of cAMP-response element binding protein (CREB), and the protein expression of CRE-regulatory genes, c-fos and COX-2 in young and senescent HDFs
16672767In young HDFs, CREB phosphorylation decreased following LPA treatment, and both c-fos and COX-2 protein levels increased rapidly
16672767However, LPA-dependent slope of luciferase increased more rapidly in senescent cells than in young cells, presumably due to an increase of LPA-induced CREB phosphorylation
8803927The promoter also contains sites for inducible transcription factors, cAMP-responsive element (CRE)-binding protein (CREB), and Activator protein 2 (AP-2)
8760066The abundance of the cAMP response element binding protein (CREB), a transcription factor which enhances gene expression when phosphorylated by protein kinase A, was markedly decreased in both whole cell and nuclear extracts of senescent cells, in both Western blotting and in gel retardation assays
8760066Also, PGE1-induced phosphorylation of CREB by protein kinase A was markedly attenuated in senescent cells
8760066There is a marked decrement in expression of CREB with senescence, and the results suggest the possibility that the diminished expression of CREB may contribute to altered cAMP-mediated regulation of gene expression with senescence
Entries Per Page
Displaying Page of