HCSGD entry for CENPA


1. General information

Official gene symbolCENPA
Entrez ID1058
Gene full namecentromere protein A
Other gene symbolsCENP-A CenH3
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000132Establishment of mitotic spindle orientationIMPbiological_process
GO:0000278Mitotic cell cycleTASbiological_process
GO:0000775Chromosome, centromeric regionIDAcellular_component
GO:0000778Condensed nuclear chromosome kinetochoreIDAcellular_component
GO:0000780Condensed nuclear chromosome, centromeric regionIDAcellular_component
GO:0000786NucleosomeIEAcellular_component
GO:0000939Condensed chromosome inner kinetochoreIEAcellular_component
GO:0003677DNA bindingIEAmolecular_function
GO:0003682Chromatin bindingTASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusTAScellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005829CytosolTAScellular_component
GO:0006334Nucleosome assemblyIEA TASbiological_process
GO:0016032Viral processIEAbiological_process
GO:0034080CENP-A containing nucleosome assembly at centromereTASbiological_process
GO:0046982Protein heterodimerization activityIEAmolecular_function
GO:0051382Kinetochore assemblyIDAbiological_process
GO:0071459Protein localization to chromosome, centromeric regionIDAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.98654356980.00041039090.99999024730.0380348592

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

Data sourceUp or downLog fold change
GSE11954Down-0.3351747949
GSE13712_SHEARDown-0.0163445450
GSE13712_STATICDown-0.4131253150
GSE19018Down-0.0325652830
GSE19899_A1Down-0.8137814279
GSE19899_A2Down-3.7577659085
PubMed_21979375_A1Down-1.3705329901
PubMed_21979375_A2Down-2.9193875586
GSE35957Down-1.8420494508
GSE36640Down-2.8708657977
GSE54402Down-0.6583593382
GSE9593Down-0.5470912585
GSE43922--
GSE24585--
GSE37065--
GSE28863_A1Down-0.2746013477
GSE28863_A2Up0.9798638293
GSE28863_A3Down-0.1803430247
GSE28863_A4Up0.1208974052
GSE48662Down-1.7116304283

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-215-5pMIMAT0000272MIRT024281MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026545MicroarrayFunctional MTI (Weak)19074876
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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

23292286Holliday junction recognition protein (HJURP), a centromere protein-A (CENP-A) histone chaperone, mediates centromere-specific assembly of CENP-A nucleosome, contributing to high-fidelity chromosome segregation during cell division
22132080RESULTS: Analysis of heterochromatin distribution in bovine senescent cells using fluorescent in situ hybridization for pericentric chromosomal regions, immunostaining of H3K9me3, centromeric proteins CENP A/B and DNA methylation showed a lower level of heterochromatin condensation as compared to young cells
20160010CENP-A reduction induces a p53-dependent cellular senescence response to protect cells from executing defective mitoses
20160010We examined chromatin structure in senescent human primary fibroblasts and found that CENP-A protein levels are diminished in senescent cells
20160010Senescence-associated reduction of CENP-A is caused by transcriptional and posttranslational control
20160010Surprisingly, forced reduction of CENP-A by short-hairpin RNA was found to cause premature senescence in human primary fibroblasts
20160010This premature senescence is dependent on a tumor suppressor, p53, but not on p16(INK4a)-Rb; the depletion of CENP-A in p53-deficient cells results in aberrant mitosis with chromosome missegregation
20160010We propose that p53-dependent senescence that arises from CENP-A reduction acts as a "self-defense mechanism" to prevent centromere-defective cells from undergoing mitotic proliferation that potentially leads to massive generation of aneuploid cells
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