HCSGD entry for ETS2


1. General information

Official gene symbolETS2
Entrez ID2114
Gene full namev-ets erythroblastosis virus E26 oncogene homolog 2 (avian)
Other gene symbolsETS2IT1
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:0000977RNA polymerase II regulatory region sequence-specific DNA bindingIEAmolecular_function
GO:0001501Skeletal system developmentTASbiological_process
GO:0003677DNA bindingTASmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA IEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0035259Glucocorticoid receptor bindingIEAmolecular_function
GO:0045893Positive regulation of transcription, DNA-templatedIDAbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.01340855210.47872665170.28899141461.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0814635406
GSE13712_SHEARDown-0.5620943515
GSE13712_STATICDown-0.3031194353
GSE19018Up0.4333201320
GSE19899_A1Up0.5761778573
GSE19899_A2Up0.5349485127
PubMed_21979375_A1Up1.0229949904
PubMed_21979375_A2Up1.4734792005
GSE35957Down-0.1752617257
GSE36640Up0.3411528955
GSE54402Up0.1398660065
GSE9593Up0.0187933994
GSE43922Up0.6471384444
GSE24585Down-0.5037976868
GSE37065Up0.4030108149
GSE28863_A1Up0.2725033436
GSE28863_A2Up0.5964986606
GSE28863_A3Down-0.3992190044
GSE28863_A4Up0.1221365628
GSE48662Down-0.3385181995

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-199a-3pMIMAT0000232MIRT000775Microarray//Northern blotFunctional MTI (Weak)16331254
hsa-miR-199a-5pMIMAT0000231MIRT004398Microarray//Northern blotFunctional MTI (Weak)16331254
hsa-miR-218-5pMIMAT0000275MIRT024245SequencingFunctional MTI (Weak)20371350
hsa-miR-877-5pMIMAT0004949MIRT037225CLASHFunctional MTI (Weak)23622248
hsa-miR-149-5pMIMAT0000450MIRT045544CLASHFunctional MTI (Weak)23622248
hsa-miR-18a-5pMIMAT0000072MIRT050649CLASHFunctional 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: 7 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25670864Structural insights into the autoregulation and cooperativity of the human transcription factor Ets-2
25670864Ets-2, like its closely related homologue Ets-1, is a member of the Ets family of DNA binding transcription factors
25670864In contrast to Ets-1, in which the autoinhibition is caused by a combination of allosteric and steric mechanisms, we were unable to find clear evidence for the allosteric mechanism in Ets-2
21763315RuvBl2 cooperates with Ets2 to transcriptionally regulate hTERT in colon cancer
21763315Using SILAC-proteomic analysis and molecular studies, we identified the AAA+ ATPase, RuvBl2 as a transcriptional regulator of hTERT and established that this regulation is through cooperation with Ets-2
19656618HBx induced DNA hypermethylation of p16(INK4a) promoter and subsequently interfered action of transcription factors like Ets1 and Ets2 activated by H(2)O(2) through the p38(MAPK) pathway, resulting in inhibition of its transcription
19340300Of these, 56 are annotated as transcription factors, including two previously reported activators of the locus, ETS2 and JUNB
17986575Ets2 may also play an important role in regulating the hTERT gene; but further studies are required to decipher the mechanisms in the regulation of telomerase activity
15659210Senescence was accompanied by a decline in transcript levels of the polycomb gene Bmi-1, Ets1 and Ets2 transcription factors, and Id1, Id2 and Id3 helix-loop-helix proteins, suggesting roles for these genes in maintenance of cardiomyocyte proliferative capacity
11234019Here we demonstrate a role for the Ets1 and Ets2 transcription factors based on their ability to activate the p16INK4a promoter through an ETS-binding site and their patterns of expression during the lifespan of human diploid fibroblasts
11234019The induction of p16INK4a by Ets2, which is abundant in young human diploid fibroblasts, is potentiated by signalling through the Ras-Raf-MEK kinase cascade and inhibited by a direct interaction with the helix-loop-helix protein Id1 (ref
11234019In senescent cells, where the Ets2 levels and MEK signalling decline, the marked increase in p16INK4a expression is consistent with the reciprocal reduction of Id1 and accumulation of Ets1
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