BMI1
Polycomb complex protein BMI-1
Also known as: BMI1_HUMAN, PCGF4, RNF51
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P35226
- Gene
- BMI1
- Ensembl
- ENSG00000168283
- Chromosome
- 10
- Canonical length
- 326 aa
- Protein class
- Cancer-related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nuclear bodies,Cytosol
OverviewNCBI Gene
This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
326 residues, UniProt reviewed canonical sequence.
>P35226|BMI1
1 MHRTTRIKIT ELNPHLMCVL CGGYFIDATT IIECLHSFCK TCIVRYLETS KYCPICDVQV
61 HKTRPLLNIR SDKTLQDIVY KLVPGLFKNE MKRRRDFYAA HPSADAANGS NEDRGEVADE
121 DKRIITDDEI ISLSIEFFDQ NRLDRKVNKD KEKSKEEVND KRYLRCPAAM TVMHLRKFLR
181 SKMDIPNTFQ IDVMYEEEPL KDYYTLMDIA YIYTWRRNGP LPLKYRVRPT CKRMKISHQR
241 DGLTNAGELE SDSGSDKANS PAGGIPSTSS CLPSPSTPVQ SPHPQFPHIS STMNGTSNSP
301 SGNHQSSFAN RPRKSSVNGS SATSSGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BMI1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.47
- Highest tissue expression
- 54 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 54 nTPM
- skeletal muscle: 42 nTPM
- retina: 37 nTPM
- spleen: 34 nTPM
- smooth muscle: 34 nTPM
- breast: 34 nTPM
Single-cell type
- late spermatids: 265 nCPM
- early spermatids: 183 nCPM
- parietal cells: 51 nCPM
- plasma cells: 51 nCPM
- gastric progenitor cells: 47 nCPM
- smooth muscle cells: 46 nCPM
Immune cell
- basophil: 15 nTPM
- MAIT T-cell: 7.1 nTPM
- memory CD4 T-cell: 5.4 nTPM
- gdT-cell: 5.2 nTPM
- NK-cell: 5.2 nTPM
- memory CD8 T-cell: 5 nTPM
Brain region
- white matter: 76 nTPM
- basal ganglia: 56 nTPM
- medulla oblongata: 49 nTPM
- midbrain: 47 nTPM
- spinal cord: 46 nTPM
- cerebellum: 46 nTPM
ReferencesPubMed · IEDB
Publications for BMI1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
4 publications
- A Panel of Tumor-associated Autoantibodies for the Detection of Early-stage Breast Cancer.
2021 · J Cancer · RCR 1 · 16 citations - Prognostic relevance of Bmi-1 expression and autoantibodies in esophageal squamous cell carcinoma.
2010 · BMC Cancer · RCR 1 · 37 citations - BMI-1 autoantibody as a new potential biomarker for cervical carcinoma.
2011 · PLoS One · RCR 0.6 · 23 citations - BMI-1 autoantibody in serum as a new potential biomarker of nasopharyngeal carcinoma.
2008 · Cancer Biol Ther · RCR 0.3 · 12 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.35
- gnomAD pLI
- 0.94
- gnomAD missense Z
- 2.43
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic signaling pathway
- brain development
- cellular response to dexamethasone stimulus
- cellular response to interleukin-1
- chromatin remodeling
- DNA methylation-dependent constitutive heterochromatin formation
- embryonic skeletal system morphogenesis
- hemopoiesis
- humoral immune response
- in utero embryonic development
- negative regulation of apoptotic signaling pathway
- negative regulation of gene expression, epigenetic
- negative regulation of transcription by RNA polymerase II
- positive regulation of B cell proliferation
- positive regulation of fibroblast proliferation
- positive regulation of immature T cell proliferation in thymus
- positive regulation of ubiquitin-protein transferase activity
- regulation of adaxial/abaxial pattern formation
- regulation of gene expression
- regulation of kidney development
- rostrocaudal neural tube patterning
- segment specification
- somatic stem cell division
Molecular functions
- promoter-specific chromatin binding
- RING-like zinc finger domain binding
- ubiquitin-protein transferase activator activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BMI1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads BMI1 as an antibody target. Whether an autoantibody or antibody against BMI1 could matter depends on whether native BMI1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BMI1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label BMI1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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