HCSGD entry for PBRM1


1. General information

Official gene symbolPBRM1
Entrez ID55193
Gene full namepolybromo 1
Other gene symbolsBAF180 PB1
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:0000228Nuclear chromosomeNAScellular_component
GO:0000776KinetochoreIEAcellular_component
GO:0001890Placenta developmentIEAbiological_process
GO:0003677DNA bindingIEAmolecular_function
GO:0003682Chromatin bindingIEA NASmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0006338Chromatin remodelingTASbiological_process
GO:0006351Transcription, DNA-templatedIEAbiological_process
GO:0006355Regulation of transcription, DNA-templatedIEAbiological_process
GO:0007067MitosisTASbiological_process
GO:0007507Heart developmentIEAbiological_process
GO:0008285Negative regulation of cell proliferationIMPbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.96299555870.04827924090.99999024730.4115048867

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

Data sourceUp or downLog fold change
GSE11954Down-0.3675622104
GSE13712_SHEARUp0.0315793398
GSE13712_STATICDown-0.2514975740
GSE19018Down-0.3345399003
GSE19899_A1Down-0.3236334321
GSE19899_A2Down-0.4611563085
PubMed_21979375_A1Down-0.5146210030
PubMed_21979375_A2Down-0.2855791703
GSE35957Down-0.1207666039
GSE36640Down-0.5740687164
GSE54402Down-0.0156520743
GSE9593Down-0.1435970714
GSE43922Down-0.2160243187
GSE24585Up0.0477760026
GSE37065Down-0.0710472068
GSE28863_A1Up0.5712888665
GSE28863_A2Up0.4890217331
GSE28863_A3Down-0.0749273148
GSE28863_A4Down-0.1509017990
GSE48662Down-0.1776105627

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-30a-5pMIMAT0000087MIRT005153pSILAC//Proteomics;OtherFunctional MTI (Weak)18668040
hsa-miR-155-5pMIMAT0000646MIRT020793ProteomicsFunctional MTI (Weak)18668040
hsa-miR-155-5pMIMAT0000646MIRT020793Reporter assay;OtherNon-Functional MTI20584899
hsa-miR-93-5pMIMAT0000093MIRT028017SequencingFunctional MTI (Weak)20371350
hsa-miR-21-5pMIMAT0000076MIRT030867MicroarrayFunctional MTI (Weak)18591254
hsa-miR-1229-3pMIMAT0005584MIRT036263CLASHFunctional MTI (Weak)23622248
hsa-miR-1226-3pMIMAT0005577MIRT036515CLASHFunctional MTI (Weak)23622248
hsa-miR-877-3pMIMAT0004950MIRT036962CLASHFunctional 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

26992241BAF180 (also called PBRM1), a subunit of the SWI/SNF complex, plays critical roles in the regulation of chromatin remodeling and gene transcription, and is frequently mutated in several human cancers
26992241However, the role of mammalian BAF180 in tumor suppression and tissue maintenance in vivo remains largely unknown
26992241Here, using a conditional somatic knockout approach, we explored the cellular and organismal functions of BAF180 in mouse
26992241BAF180 deletion in primary mouse embryonic fibroblasts (MEFs) triggers profound cell cycle arrest, premature cellular senescence, without affecting DNA damage response or chromosomal integrity
26992241While somatic deletion of BAF180 in adult mice does not provoke tumor development, BAF180 deficient mice exhibit defects in hematopoietic system characterized by progressive reduction of hematopoietic stem cells (HSCs), defective long-term repopulating potential, and hematopoietic lineage developmental aberrations
26992241BAF180 deletion results in elevated p21 expression in both MEFs and HSCs
26992241Mechanistically, we showed that BAF180 binds to p21 promoter, and BAF180 deletion enhances the binding of modified histones associated with transcriptional activation on p21 promoter
26992241Deletion of p21 rescues cell cycle arrest and premature senescence in BAF180 deficient MEFs, and partially rescues hematopoietic defects in BAF180 deficient mice
26992241Together, our study identifies BAF180 as a critical regulator of cellular senescence and HSC homeostasis, which is at least partially regulated through BAF180-mediated suppression of p21 expression
26992241Our results also suggest that senescence triggered by BAF180 inactivation may serve as a failsafe mechanism to restrain BAF180 deficiency-associated tumor development, providing a conceptual framework to further understand BAF180 function in tumor biology
20660729Polybromo-associated BRG1-associated factor components BRD7 and BAF180 are critical regulators of p53 required for induction of replicative senescence
20660729Here we describe BRD7 and BAF180 as unique regulators of replicative senescence in human cells
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