HCSGD entry for E2F2


1. General information

Official gene symbolE2F2
Entrez ID1870
Gene full nameE2F transcription factor 2
Other gene symbolsE2F-2
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000278Mitotic cell cycleTASbiological_process
GO:0001047Core promoter bindingIDAmolecular_function
GO:0003677DNA bindingTASmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005654NucleoplasmTAScellular_component
GO:0005667Transcription factor complexIEAcellular_component
GO:0006367Transcription initiation from RNA polymerase II promoterTASbiological_process
GO:0008134Transcription factor bindingIPImolecular_function
GO:0051726Regulation of cell cycleIEAbiological_process
GO:0072332Intrinsic apoptotic signaling pathway by p53 class mediatorIEAbiological_process
GO:1990086Lens fiber cell apoptotic processIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.96923738460.05598914550.99999024730.4446561388

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

Data sourceUp or downLog fold change
GSE11954Down-0.0680039174
GSE13712_SHEARDown-0.1880925657
GSE13712_STATICDown-0.2294529459
GSE19018Up0.0062463974
GSE19899_A1Down-0.0108411934
GSE19899_A2Down-0.2639106094
PubMed_21979375_A1Down-0.4377436113
PubMed_21979375_A2Down-0.1947203624
GSE35957Down-0.0810038791
GSE36640Down-1.2979742432
GSE54402Down-0.1808079053
GSE9593Down-0.0064966833
GSE43922Up0.0749088778
GSE24585Up0.1428034989
GSE37065Down-0.1289189598
GSE28863_A1Down-0.1740163115
GSE28863_A2Up0.2769303702
GSE28863_A3Up0.1909901777
GSE28863_A4Up0.0383916426
GSE48662Down-2.0303966798

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-24-3pMIMAT0000080MIRT000122Luciferase reporter assay//Microarray//qRT-PCR//Western blot//Western blot;qRT-PCR;Microarray;OtherFunctional MTI19748357
hsa-miR-21-5pMIMAT0000076MIRT001121Northern blot//qRT-PCR//ChIPFunctional MTI (Weak)19528081
hsa-miR-98-5pMIMAT0000096MIRT001126Northern blot//Western blot//qRT-PCR//ChIP//Luciferase reporter assayFunctional MTI19528081
hsa-let-7a-5pMIMAT0000062MIRT005477Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI20418948
hsa-miR-125b-5pMIMAT0000423MIRT006974Luciferase reporter assay//qRT-PCR//Western blotFunctional MTI22999819
hsa-miR-193b-3pMIMAT0002819MIRT016577MicroarrayFunctional MTI (Weak)20304954
hsa-miR-155-5pMIMAT0000646MIRT021062Reporter assay;OtherFunctional MTI20584899
hsa-miR-155-5pMIMAT0000646MIRT021062Reporter assay;OtherNon-Functional MTI19759154
hsa-miR-22-3pMIMAT0000077MIRT030648SequencingFunctional MTI (Weak)20371350
hsa-miR-331-3pMIMAT0000760MIRT043574CLASHFunctional MTI (Weak)23622248
hsa-miR-7-5pMIMAT0000252MIRT047757CLASHFunctional MTI (Weak)23622248
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  • mirRecord

MicroRNA name

mirBase ID

Target site number

MiRNA mature ID

Test method inter

MiRNA regulation site

Reporter target site

Pubmed ID

hsa-miR-24-3pMIMAT00000801hsa-miR-24{Western blot}{overexpression by miRNA mimics tranfection}19748357
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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

27081696Serial gene expression analyses with SK-Hep1 liver cancer cells treated with JQ1 to delineate the key player of BRD4 inhibition identified E2F2 as the first line of downstream direct target of BRD4
27081696Further experiments including chromatin immunoprecipitation (ChIP) assay and loss of function study confirmed E2F2 as key player of BRD4 inhibition
25772242We show that MOZ is required to maintain normal levels of histone 3 lysine 9 (H3K9) and H3K27 acetylation at the transcriptional start sites of at least four genes, Cdc6, Ezh2, E2f2 and Melk, and normal mRNA levels of these genes
25772242CDC6, EZH2 and E2F2 are known inhibitors of the INK4A-ARF pathway
11640890Expression by recombinant adenovirus of E2F1, E2F2, E2F3, cyclin E/cdk2, and Mdm2 individually resulted in DNA synthesis in 10-30% of cells
10585280Here we present evidence that activation of a cAMP pathway correlates with multiple cellular changes in these cells: (1) increased expression of the transcription factor microphthalmia; (2) increased melanogenesis; (3) increased association of the cyclin-dependent kinase inhibitors (CDK-Is) p27(KIP1) and p16(INK4) with CDK2 and CDK4, respectively; (4) failure to phosphorylate the retinoblastoma protein (pRB); (5) decreased expression of E2F1, E2F2, and E2F4 proteins; (6) loss of E2F DNA-binding activity; and (7) phenotypic changes characteristic of senescent cells
8816912In contrast, E2F-2 mRNA was not detectable in IMR-90 or WI-38 human fibroblasts
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