HCSGD entry for SIN3B


1. General information

Official gene symbolSIN3B
Entrez ID23309
Gene full nameSIN3 transcription regulator homolog B (yeast)
Other gene symbols
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:0000805X chromosomeIEAcellular_component
GO:0000806Y chromosomeIEAcellular_component
GO:0001741XY bodyIEAcellular_component
GO:0003682Chromatin bindingIEAmolecular_function
GO:0003714Transcription corepressor activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEA ISScellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005737CytoplasmIEAcellular_component
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedIEAbiological_process
GO:0007519Skeletal muscle tissue developmentIEAbiological_process
GO:0030849AutosomeIEAcellular_component
GO:0044255Cellular lipid metabolic processTASbiological_process
GO:0044281Small molecule metabolic processTASbiological_process
GO:0045892Negative regulation of transcription, DNA-templatedIEAbiological_process
GO:0048738Cardiac muscle tissue developmentIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.10884918130.95000163370.68348533271.0000000000

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

Data sourceUp or downLog fold change
GSE11954Down-0.0454418531
GSE13712_SHEARUp0.1624942218
GSE13712_STATICUp0.1042289499
GSE19018Down-0.0435706399
GSE19899_A1Down-0.0700256466
GSE19899_A2Up0.7204016011
PubMed_21979375_A1Up0.1353095368
PubMed_21979375_A2Up1.0824914673
GSE35957Down-0.0396877198
GSE36640Up0.6024930728
GSE54402Up0.0962623894
GSE9593Up0.2395605584
GSE43922Up0.0966844128
GSE24585Down-0.1678105058
GSE37065Down-0.1018932599
GSE28863_A1Up0.1566892206
GSE28863_A2Up0.1908457684
GSE28863_A3Down-0.0239743555
GSE28863_A4Down-0.0253528570
GSE48662Up0.5432367873

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-335-5pMIMAT0000765MIRT019064MicroarrayFunctional MTI (Weak)18185580
hsa-miR-186-5pMIMAT0000456MIRT045249CLASHFunctional MTI (Weak)23622248
hsa-miR-92a-3pMIMAT0000092MIRT049321CLASHFunctional 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: 3 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

27308374SIN3B, the SASP, and pancreatic cancer
25263442Transcriptional repression of Sin3B by Bmi-1 prevents cellular senescence and is relieved by oncogene activation
25263442The expression of the chromatin-associated Sin3B protein is stimulated by oncogenic stress, and is required for oncogene-induced senescence
25263442Here we demonstrate that oncogenic stress leads to the dissociation of Bmi-1 from the Sin3B locus, resulting in increased Sin3B expression and subsequent entry into cellular senescence
25263442Furthermore, Sin3B is required for the senescent phenotype and elevated levels of reactive oxygen species elicited upon Bmi-1 depletion
25263442Altogether, these results identify Sin3B as a novel direct target of Bmi-1, and establish Bmi-1-driven repression of Sin3B as an essential regulator of cellular senescence
19654306Sin3B expression is required for cellular senescence and is up-regulated upon oncogenic stress
19654306We show that fibroblasts genetically inactivated for the chromatin-associated Sin3B protein are refractory to replicative and oncogene-induced senescence
19654306Conversely, overexpression of Sin3B triggers senescence and the formation of senescence-associated heterochromatic foci
19654306Although Sin3B is strongly up-regulated upon oncogenic stress, decrease in expression of Sin3B is associated with tumor progression in vivo, suggesting that expression of Sin3B may represent a barrier against transformation
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