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BIRC6 (Baculoviral IAP repeat-containing 6)

Identity

Other namesBaculoviral IAP repeat-containing ubiquitin-conjugating enzyme (BRUCE)
Baculoviral IAP repeat-containing 6 (Apollon)
FLJ13726
FLJ13786
KIAA1289
HGNC BIRC6
Location 2p22
Local_order CARD12 (caspase recruitment domain family member 12) {encoded on minus strand, 32.303.029-32.344.427}
YPF4 (YIP1 domain family member 4) {32.356.483-32.385.159}
BIRC6 {32.435.234-32.697.467}
TTC27 (tetratricopeptide repeat domain 27) {32.706.633-32.899.620}
LTBP1 (latent transforming growth factor beta binding protein 1) {33.025.896-33.478.077}

DNA/RNA

Description The BIRC6 gene comprises 75 exons resulting in a transcript of 16066 bps. The ATG is in the first exon.
Transcription Only one variant of BIRC6 has been found so far which comprises 14490 bps. There are several synonymous and nonsynonymous SNPs reported for BIRC6 (E589K, L1742F, R2187T, T2646S, T3708N, E3864K, Q4323H, N4324Y, S4325C, N4326T, P4329R).
Pseudogene Not known. There is evidence for a processed pseudogene in M. musculus.

Protein

 
  BRUCE is component of the apoptosis regulatory network. Multiple protein-protein interactions allow a switch from apoptosis inhibition to inactivation in later steps in apoptosis. BRUCEšs action on activated caspases and other pro-apoptotic molecules might be restricted to the trans-Golgi network and the vesicular system.
Description BIRC6 contains two functionally validated domains: A N-terminal BIR repeat (SMART SM00238, aa: 256-332) and a C-terminal UBC domain (SMART SM00212, aa: 4548 ­ 4712). The BIR repeat is needed for interactions with caspases and IAP-binding motiv (IBM) containing proteins (HtrA2, Smac). The UBC domain can form a thiolester linkage with ubiquitin transferred by E1.
Between aa 1589-1633 a coiled-coil region can be found.
Expression BRUCE is highly expressed in brain, testis, lymphatic cells and secretory organs and also found in any other tissue. It is highly expressed in the mouse embryos up to E11 and then transcript levels drop.
Localisation Localized to membranes of the trans Golgi network (TGN) and the endosomal system.
Function BRUCE is a peripheral membrane protein of the trans-Golgi network that protects cells from apoptosis by functioning as an inhibitor of apoptosis protein (IAP). BRUCE can bind and inhibit activated caspases CASP-3, CASP-6, CASP-7, CASP-8 and CASP-9. Furthermore it ubiquitylates caspase-9, HtrA2 (a pro-apoptotic serine protease) and DIABLO/Smac (a competitor for caspase-IAP interactions) thereby most likely targeting them for proteasomal degradation. The ubiquityltion reactions do not require an ubiquitin E3 ligase making BRUCE a chimeric E2/E3 ubiquitin ligase.
Homology ubc-17 (C. elegans)
IAP6 (A. gambiae)
Bruce (D. melanogaster)
BIRC6 (X. tropicalis)
Birc6 (M. musculus).

Mutations

Note There are several synonymous and nonsynonymous SNPs reported for BIRC6 (E589K, L1742F, R2187T, T2646S, T3708N, E3864K, Q4323H, N4324Y, S4325C, N4326T, P4329R).

Implicated in

Entity Overexpression of BRUCE is found in several cancer cell lines (brain SF-268, SNB-78 ­ ovarian cancer OVCAR-8). High level expression of BRUCE in these cell lines seems to correlate with their resistance to apoptotic reagents. Furthermore, bone marrow cells of myelodysplastic syndromes exhibit significant expression of BIRC6.
  

External links

Nomenclature
HGNCBIRC6   13516
Entrez_GeneBIRC6  57448  baculoviral IAP repeat-containing 6
Cards
AtlasBIRC6ID798ch2p22
GeneCardsBIRC6
EnsemblBIRC6 [Search_View]   ENSG00000115760 [Gene_View]
GenatlasBIRC6
GeneLynxBIRC6
eGenomeBIRC6
euGene57448
Genomic and cartography
GoldenPathBIRC6  -  2p22   chr2:32435600-32697469 +  2p22.3   [Description]    (hg18-Mar_2006)
EnsemblBIRC6 - 2p22.3 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneBIRC6
Gene and transcription
GenbankAA315620 [ ENTREZ ]
GenbankAB033115 [ ENTREZ ]
GenbankAF265555 [ ENTREZ ]
GenbankAK023788 [ ENTREZ ]
GenbankAK023848 [ ENTREZ ]
RefSeqNM_016252 [ SRS ]    NM_016252 [ ENTREZ ]
RefSeqAC_000045 [ SRS ]    AC_000045 [ ENTREZ ]
RefSeqAC_000134 [ SRS ]    AC_000134 [ ENTREZ ]
RefSeqNC_000002 [ SRS ]    NC_000002 [ ENTREZ ]
RefSeqNT_022184 [ SRS ]    NT_022184 [ ENTREZ ]
RefSeqNW_001838769 [ SRS ]    NW_001838769 [ ENTREZ ]
RefSeqNW_927719 [ SRS ]    NW_927719 [ ENTREZ ]
AceViewBIRC6 AceView - NCBI
UnigeneHs.150107 [ SRS ]    Hs.150107 [ NCBI ]     HS150107 [ spliceNest ]
Fast-db3875 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtQ9H8B7 [ SRS]    Q9H8B7 [ EXPASY ]     Q9H8B7 [ INTERPRO ]     Q9H8B7 [ UNIPROT ]
PrositePS50127 UBIQUITIN_CONJUGAT_2 [ SRS ]    PS50127 UBIQUITIN_CONJUGAT_2 [ Expasy ]
InterproIPR016135 UBQ-conjugat/RWD-like [ SRS ]    IPR016135 UBQ-conjugat/RWD-like [ EBI ]
InterproIPR000608 UBQ-conjugat_E2 [ SRS ]    IPR000608 UBQ-conjugat_E2 [ EBI ]
CluSTrQ9H8B7
PfamPF00179 UQ_con [ SRS ]    PF00179 UQ_con [ Sanger ]    pfam00179 [ NCBI-CDD ]
SmartSM00212 UBCc [EMBL]
ProdomPD000461 UBQ_conjugat[INRA-Toulouse]
ProdomQ9H8B7 Q9H8B7_HUMAN [ Domain structure ]   Q9H8B7 Q9H8B7_HUMAN  [ sequences sharing at least 1 domain ]
BlocksQ9H8B7
HPRD05731
Protein Interaction databases
DIPQ9H8B7
IntActQ9H8B7
Polymorphism : SNP, mutations, diseases
OMIM605638    [ map ]   
GENECLINICS605638
SNPBIRC6 [dbSNP-NCBI]  
SNPNM_016252 [SNP-NCI]  
SNPBIRC6 [GeneSNPs - Utah]  BIRC6] [HGBASE - SRS]
HAPMAPBIRC6 [HAPMAP]  
COSMICBIRC6 [Somatic mutation (COSMIC-CGP-Sanger)]  
HGMDBIRC6
General knowledge
Family BrowserBIRC6 [UCSC Family Browser]
SOURCENM_016252
SMDHs.150107
SAGEHs.150107
GOubiquitin-protein ligase activity [Amigo]  ubiquitin-protein ligase activity
GOcysteine protease inhibitor activity [Amigo]  cysteine protease inhibitor activity
GOprotein binding [Amigo]  protein binding
GOcellular_component [Amigo]  cellular_component
GOintracellular [Amigo]  intracellular
GOmembrane fraction [Amigo]  membrane fraction
GOapoptosis [Amigo]  apoptosis
GOanti-apoptosis [Amigo]  anti-apoptosis
GOpositive regulation of cell proliferation [Amigo]  positive regulation of cell proliferation
GOligase activity [Amigo]  ligase activity
GOregulation of protein metabolic process [Amigo]  regulation of protein metabolic process
PubGeneBIRC6
TreeFamBIRC6
CTD57448 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeBIRC6 Related clones (RZPD - Berlin)
PubMed
PubMed12 Pubmed reference(s) in LocusLink

Bibliography

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Drosophila Bruce can potently suppress Rpr- and Grim-dependent but not Hid-dependent cell death.
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Dual role of BRUCE as an antiapoptotic IAP and a chimeric E2/E3 ubiquitin ligase.
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PMID 15200957
 
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PMID 14765125
 
Bone marrow cells of myelodysplastic syndromes exhibit significant expression of apollon, livin and ILP-2 with reduction after transformation to overt leukemia.
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Progressive loss of the spongiotrophoblast layer of Birc6/Bruce mutants results in embryonic lethality.
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HtrA2 cleaves Apollon and induces cell death by IAP-binding motif in Apollon-deficient cells.
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PMID 15781261
 
Bruce/apollon promotes hippocampal neuron survival and is downregulated by kainic acid.
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Comparative study of gene expression by cDNA microarray in human colorectal cancer tissues and normal mucosa.
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PMID 16773188
 
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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Contributor(s)

Written11-2006Christian Pohl, Stefan Jentsch

Citation

This paper should be referenced as such :
Pohl C, Jentsch S . BIRC6 (Baculoviral IAP repeat-containing 6). Atlas Genet Cytogenet Oncol Haematol. November 2006 .
URL : http://AtlasGeneticsOncology.org/Genes/BIRC6ID798ch2p22.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Aug 11 21:12:30 2008


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