HCSGD entry for BUB1B


1. General information

Official gene symbolBUB1B
Entrez ID701
Gene full nameBUB1 mitotic checkpoint serine/threonine kinase B
Other gene symbolsBUB1beta BUBR1 Bub1A MAD3L MVA1 SSK1 hBUBR1
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:0000278Mitotic cell cycleTASbiological_process
GO:0000776KinetochoreIDA NAS TAScellular_component
GO:0000777Condensed chromosome kinetochoreIDAcellular_component
GO:0000778Condensed nuclear chromosome kinetochoreIEAcellular_component
GO:0000940Condensed chromosome outer kinetochoreIDAcellular_component
GO:0004672Protein kinase activityNASmolecular_function
GO:0004674Protein serine/threonine kinase activityIEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005524ATP bindingIEAmolecular_function
GO:0005680Anaphase-promoting complexTAScellular_component
GO:0005737CytoplasmIDAcellular_component
GO:0005815Microtubule organizing centerIEAcellular_component
GO:0005829CytosolTAScellular_component
GO:0006915Apoptotic processIEAbiological_process
GO:0007049Cell cycleNASbiological_process
GO:0007051Spindle organizationNASbiological_process
GO:0007067MitosisNASbiological_process
GO:0007091Metaphase/anaphase transition of mitotic cell cycleIEAbiological_process
GO:0007093Mitotic cell cycle checkpointTASbiological_process
GO:0007094Mitotic spindle assembly checkpointTASbiological_process
GO:0008283Cell proliferationTASbiological_process
GO:0031145Anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic processTASbiological_process
GO:0034501Protein localization to kinetochoreIPIbiological_process
GO:0048015Phosphatidylinositol-mediated signalingNASbiological_process
GO:0048471Perinuclear region of cytoplasmIDAcellular_component
GO:0051233Spindle midzoneNAScellular_component
GO:0051436Negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycleTASbiological_process
GO:0051439Regulation of ubiquitin-protein ligase activity involved in mitotic cell cycleTASbiological_process
GO:0071459Protein localization to chromosome, centromeric regionIEAbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.99805748260.00000598000.99999024730.0069833333

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

Data sourceUp or downLog fold change
GSE11954Down-1.2427376203
GSE13712_SHEARDown-0.4195506243
GSE13712_STATICDown-0.1913959824
GSE19018Up0.0503095882
GSE19899_A1Down-2.6716479688
GSE19899_A2Down-4.8536456297
PubMed_21979375_A1Down-4.5286531805
PubMed_21979375_A2Down-5.8808263208
GSE35957Down-5.4824434440
GSE36640Down-5.3740809223
GSE54402Down-1.3751989605
GSE9593Down-2.4122174283
GSE43922Down-2.8587823445
GSE24585Down-0.5525487472
GSE37065Down-1.0427748825
GSE28863_A1--
GSE28863_A2--
GSE28863_A3--
GSE28863_A4--
GSE48662Down-1.7698664734

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-3pMIMAT0002819MIRT016386MicroarrayFunctional MTI (Weak)20304954
hsa-miR-193b-3pMIMAT0002819MIRT016386CLASHFunctional MTI (Weak)23622248
hsa-miR-215-5pMIMAT0000272MIRT024609MicroarrayFunctional MTI (Weak)19074876
hsa-miR-192-5pMIMAT0000222MIRT026320MicroarrayFunctional MTI (Weak)19074876
hsa-miR-22-3pMIMAT0000077MIRT050455CLASHFunctional 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

26883501In addition, tight junction coverage in microvessels and BBB integrity in BubR1 hypomorphic (BubR1(H/H)) mice, which display senescence cell-dependent phenotypes, were examined
26847209Haplo-insufficiency of both BubR1 and SGO1 accelerates cellular senescence
26847209BACKGROUND: Spindle assembly checkpoint components BubR1 and Sgo1 play a key role in the maintenance of chromosomal instability during cell division
26847209Haplo-insufficiency of either BubR1 or SGO1 results in enhanced chromosomal instability and tumor development in the intestine
26847209METHODS: We took advantage of the availability of BubR1 and SGO1 knockout mice and generated primary murine embryonic fibroblasts (MEFs) with mutations in either BubR1, SGO1, or both and analyzed cellular senescence of the MEFs of various genetic backgrounds
26847209RESULTS: We observed that BubR1(+/-) SGO(+/-) MEFs had an accelerated cellular senescence characterized by morphological changes and expressed senescence-associated beta-galactosidase
26847209In addition, compared with wild-type MEFs or MEFs with a single gene deficiency, BubR1(+/-) SGO1(+/-) MEFs expressed enhanced levels of p21 but not p16
26847209CONCLUSIONS: Taken together, our observations suggest that combined deficiency of BubR1 and Sgo1 accelerates cellular senescence
23212104The use of a progeroid mouse model (which expresses low amounts of the mitotic checkpoint protein BubR1) has been instrumental in demonstrating that p16(Ink4a)-positive senescent cells drive age-related pathologies and that selective elimination of these cells can prevent or delay age-related deterioration
22048312Here we show that in the BubR1 progeroid mouse background, INK-ATTAC removes p16(Ink4a)-positive senescent cells upon drug treatment
18769141One approach to bypass this problem would be to inactivate these pathways in a murine segmental progeria model such as mice that express low amounts of the mitotic checkpoint protein BubR1 (BubR1 hypomorphic mice)
18769141Importantly, BubR1 hypomorphism elevates both p16(Ink4a) and p19(Arf) expression in skeletal muscle and fat
18769141Inactivation of p16(Ink4a) in BubR1 mutant mice delays both cellular senescence and aging specifically in these tissues
18516091Opposing roles for p16Ink4a and p19Arf in senescence and ageing caused by BubR1 insufficiency
18516091Here, we show that skeletal muscle and fat, two tissues that develop early ageing-associated phenotypes in response to BubR1 insufficiency, have high levels of p16(Ink4a) and p19(Arf)
18516091Conversely, p19(Arf) inactivation exacerbates senescence and ageing in BubR1 mutant mice
18516091Thus, we identify BubR1 insufficiency as a trigger for activation of the Cdkn2a locus in certain mouse tissues, and demonstrate that p16(Ink4a) is an effector and p19(Arf) an attenuator of senescence and ageing in these tissues
16476774Mice that have small amounts of the mitotic checkpoint protein BubR1 age much faster than normal mice, but whether other mitotic checkpoint genes function to prevent the early onset of aging is unknown
16476774Furthermore, although BubR1 hypomorphic mice have less aneuploidy than Bub3/Rae1 haploinsufficient mice, they age much faster
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