HCSGD entry for PIAS4


1. General information

Official gene symbolPIAS4
Entrez ID51588
Gene full nameprotein inhibitor of activated STAT, 4
Other gene symbolsPIASY Piasg ZMIZ6
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:0000122Negative regulation of transcription from RNA polymerase II promoterIEAbiological_process
GO:0003677DNA bindingIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDA NAScellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0008270Zinc ion bindingNASmolecular_function
GO:0016055Wnt signaling pathwayIEAbiological_process
GO:0016363Nuclear matrixIEAcellular_component
GO:0016605PML bodyIEAcellular_component
GO:0016925Protein sumoylationIEA IMPbiological_process
GO:0019789SUMO ligase activityIDA IMPmolecular_function
GO:0031625Ubiquitin protein ligase bindingIPImolecular_function
GO:0032088Negative regulation of NF-kappaB transcription factor activityIEAbiological_process
GO:0033235Positive regulation of protein sumoylationIDAbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIDA NASbiological_process
GO:1902174Positive regulation of keratinocyte apoptotic processISSbiological_process
GO:1902231Positive regulation of intrinsic apoptotic signaling pathway in response to DNA damageIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.05343219480.93526336010.50534835131.0000000000

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

Data sourceUp or downLog fold change
GSE11954Up0.0867875749
GSE13712_SHEARUp0.0144224009
GSE13712_STATICDown-0.0281053443
GSE19018Up0.1830722225
GSE19899_A1Up0.3620777628
GSE19899_A2Up1.3964051451
PubMed_21979375_A1Up0.4169916965
PubMed_21979375_A2Up0.6949713105
GSE35957Down-0.5339573689
GSE36640Down-0.0376898142
GSE54402Up0.2209072173
GSE9593Down-0.3201975544
GSE43922Up0.3571362408
GSE24585Up0.2185602523
GSE37065Up0.0491912794
GSE28863_A1Down-0.1200417686
GSE28863_A2Down-0.2777136434
GSE28863_A3Up0.3619720986
GSE28863_A4Up0.1272380462
GSE48662Up0.1443165760

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-324-5pMIMAT0000761MIRT043227CLASHFunctional 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: 6 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

25701873This satellite cell senescence is due to accumulation of the SUMO ligase PIASy, a substrate of TRIM32
23893515Here, we determined the genome-wide localization of SUMO1 and SUMO2/3, as well as of UBC9 (encoded by UBE2I) and PIASY (encoded by PIAS4), two markers for active sumoylation, along with Pol II and histone marks in proliferating versus senescent human fibroblasts together with gene expression profiling
22505452Furthermore, TRIM32-deficient primary myoblasts underwent premature senescence and impaired myogenesis due to accumulation of PIAS4, an E3 SUMO ligase and TRIM32 substrate that was previously shown to be associated with senescence
22505452Trim32-/- muscles had substantially fewer activated satellite cells, increased PIAS4 levels, and growth failure compared with wild-type muscles
19436740Moreover, we provide evidence that PIASy functions as a specific SUMO E3-ligase for DRIL1 and promotes its sumoylation both in vitro and in vivo
19436740Furthermore, consistent with the subnuclear localization of PIASy in the Matrix-Associated Region (MAR), SUMO-modified DRIL1 species are found exclusively in the MAR fraction
17374992We have shown recently that the E3 SUMO ligase PIASy actively contributes to execution of the senescence program, thus, providing the first evidence for a direct role of SUMO modification in this process
16793547The E3 SUMO ligase PIASy is a regulator of cellular senescence and apoptosis
16793547Here we show that overexpression of the E3 SUMO ligase PIASy in normal human fibroblasts recruits the p53 and Rb tumor suppressor pathways to provoke a senescence arrest
16793547By contrast, in Rb-deficient fibroblasts, expression of PIASy leads to p53-dependent apoptosis
16793547Induction of senescence requires PIASy E3 activity and is specific for this member of the PIAS ligase family
16793547PIASy stimulates sumoylation and transcriptional activity of p53 and increases Rb-dependent corepression through recruitment to E2F-responsive promoters
16793547Viral oncoprotein E6 suppresses both PIASy-induced senescence and sumoylation of PIASy substrates
16793547Finally, we show that fibroblasts lacking PIASy exhibit a highly reduced propensity to undergo senescence in response to a prosenescence stimulus
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