HCSGD entry for MCRS1


1. General information

Official gene symbolMCRS1
Entrez ID10445
Gene full namemicrospherule protein 1
Other gene symbolsICP22BP INO80Q MCRS2 MSP58 P78
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:0000123Histone acetyltransferase complexIDAcellular_component
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIDAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005730NucleolusIDAcellular_component
GO:0005737CytoplasmTAScellular_component
GO:0006281DNA repairIEAbiological_process
GO:0006310DNA recombinationIEAbiological_process
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedIEAbiological_process
GO:0006464Cellular protein modification processTASbiological_process
GO:0031011Ino80 complexIDAcellular_component
GO:0043981Histone H4-K5 acetylationIDAbiological_process
GO:0043982Histone H4-K8 acetylationIDAbiological_process
GO:0043984Histone H4-K16 acetylationIDAbiological_process
GO:0043995Histone acetyltransferase activity (H4-K5 specific)IDAmolecular_function
GO:0043996Histone acetyltransferase activity (H4-K8 specific)IDAmolecular_function
GO:0046972Histone acetyltransferase activity (H4-K16 specific)IDAmolecular_function
GO:0071339MLL1 complexIDAcellular_component
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.87904214890.04145603510.99999024730.3832915028

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

Data sourceUp or downLog fold change
GSE11954Up0.0033076634
GSE13712_SHEARUp0.0195499662
GSE13712_STATICUp0.1139940323
GSE19018Down-0.1414610065
GSE19899_A1Down-0.5435126193
GSE19899_A2Down-0.0715406510
PubMed_21979375_A1Up0.4583062369
PubMed_21979375_A2Up0.5482985776
GSE35957Down-0.3655979580
GSE36640Down-0.7978426621
GSE54402Up0.2000813088
GSE9593Down-0.3247536022
GSE43922Down-0.0063434913
GSE24585Down-0.6045948858
GSE37065Down-0.1483321203
GSE28863_A1Down-0.0786476408
GSE28863_A2Down-0.3196710669
GSE28863_A3Down-0.6401392031
GSE28863_A4Up0.1030011939
GSE48662Down-0.0193021570

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-193b-3pMIMAT0002819MIRT041247CLASHFunctional MTI (Weak)23622248
hsa-miR-324-3pMIMAT0000762MIRT043001CLASHFunctional MTI (Weak)23622248
hsa-miR-320aMIMAT0000510MIRT044730CLASHFunctional 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: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

24361335The 58-kda microspherule protein (MSP58) represses human telomerase reverse transcriptase (hTERT) gene expression and cell proliferation by interacting with telomerase transcriptional element-interacting factor (TEIF)
2436133558-kDa microspherule protein (MSP58) plays an important role in a variety of cellular processes including transcriptional regulation, cell proliferation and oncogenic transformation
24361335Currently, the mechanisms underlying the oncogenic effect of MSP58 are not fully understood
24361335Here we identify telomerase transcriptional element-interacting factor (TEIF) as a novel MSP58-interacting protein and determine the effect of MSP58 on hTERT transcription
24361335This study thus provides evidence showing MSP58 to be a negative regulator of hTERT expression and telomerase activity
24361335Luciferase reporter assays indicated that MSP58 could suppress the transcription ofhTERTpromoter
24361335Additionally, stable overexpression of MSP58 protein in HT1080 and 293T cells decreased both endogenous hTERT expression and telomerase activity
24361335Conversely, their upregulation was induced by MSP58 silencing
24361335Chromatin immunoprecipitation assays showed that MSP58 binds to the hTERT proximal promoter
24361335The inhibitory effect of MSP58 occurred through inhibition of TEIF binding to DNA
24361335Together, our findings provide new insights into both the biological function of MSP58 and the regulation of telomerase/hTERT expression
2256307858-kDa microspherule protein (MSP58) is novel Brahma-related gene 1 (BRG1)-associated protein that modulates p53/p21 senescence pathway
22563078The nucleolar 58-kDa microspherule protein (MSP58) protein is a candidate oncogene implicated in modulating cellular proliferation and malignant transformation
22563078In this study, we show that knocking down MSP58 expression caused aneuploidy and led to apoptosis, whereas ectopic expression of MSP58 regulated cell proliferation in a context-dependent manner
22563078Specifically, ectopic expression of MSP58 in normal human IMR90 and Hs68 diploid fibroblasts, the H184B5F5/M10 mammary epithelial cell line, HT1080 fibrosarcoma cells, primary mouse embryonic fibroblasts, and immortalized NIH3T3 fibroblasts resulted in induction of premature senescence, an enlarged and flattened cellular morphology, and increased senescence-associated beta-galactosidase activity
22563078At least two senescence mechanisms are induced by MSP58
22563078First, MSP58 activates the DNA damage response and p53/p21 signaling pathways
22563078Second, MSP58, p53, and the SWI/SNF chromatin-remodeling subunit Brahma-related gene 1 (BRG1) form a ternary complex on the p21 promoter and collaborate to activate p21
22563078Additionally, MSP58 protein levels increased in cells undergoing replicative senescence and stress-induced senescence
22563078Notably, the results of analyzing expression levels of MSP58 between tumors and matched normal tissues showed significant changes (both up- and down-regulation) in its expression in various types of tumors
22563078Our findings highlight new aspects of MSP58 in modulating cellular senescence and suggest that MSP58 has both oncogenic and tumor-suppressive properties
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