BAG4

Protein-coding gene in the species Homo sapiens
BAG4
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1M62, 1M7K

Identifiers
AliasesBAG4, BAG-4, SODD, BCL2 associated athanogene 4, BAG cochaperone 4
External IDsOMIM: 603884; MGI: 1914634; HomoloGene: 31270; GeneCards: BAG4; OMA:BAG4 - orthologs
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for BAG4
Genomic location for BAG4
Band8p11.23Start38,176,533 bp[1]
End38,213,301 bp[1]
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)[2]
Chromosome 8 (mouse)
Genomic location for BAG4
Genomic location for BAG4
Band8|8 A2Start26,254,566 bp[2]
End26,275,315 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • Brodmann area 23

  • lateral nuclear group of thalamus

  • postcentral gyrus

  • germinal epithelium

  • pons

  • entorhinal cortex

  • epithelium of nasopharynx

  • superior frontal gyrus

  • Pars compacta

  • cerebellar vermis
Top expressed in
  • primary oocyte

  • dentate gyrus of hippocampal formation granule cell

  • zygote

  • Region I of hippocampus proper

  • seminiferous tubule

  • visual cortex

  • lateral septal nucleus

  • retinal pigment epithelium

  • ventromedial nucleus

  • primary visual cortex
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
  • chaperone binding
  • ubiquitin protein ligase binding
  • protein binding
  • adenyl-nucleotide exchange factor activity
  • RNA binding
Cellular component
  • cytoplasm
  • plasma membrane
  • cytosol
  • nucleus
Biological process
  • positive regulation of peptidyl-serine phosphorylation
  • positive regulation of fibroblast migration
  • negative regulation of apoptotic process
  • negative regulation of protein targeting to mitochondrion
  • cellular response to epidermal growth factor stimulus
  • positive regulation of protein kinase B signaling
  • negative regulation of phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity
  • positive regulation of stress fiber assembly
  • protein folding
  • tumor necrosis factor-mediated signaling pathway
  • positive regulation of actin filament polymerization
  • protein localization to plasma membrane
  • ruffle assembly
  • positive regulation of cell adhesion
  • regulation of cellular response to heat
  • cellular response to tumor necrosis factor
  • negative regulation of mRNA modification
  • protein heterooligomerization
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

9530

67384

Ensembl

ENSG00000156735

ENSMUSG00000037316

UniProt

O95429

Q8CI61

RefSeq (mRNA)

NM_004874
NM_001204878

NM_026121

RefSeq (protein)

NP_001191807
NP_004865

NP_080397

Location (UCSC)Chr 8: 38.18 – 38.21 MbChr 8: 26.25 – 26.28 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

BAG family molecular chaperone regulator 4 is a protein that in humans is encoded by the BAG4 gene.[5][6][7]

Function

The protein encoded by this gene is a member of the BAG1-related protein family. BAG1 is an anti-apoptotic protein that functions through interactions with a variety of cell apoptosis and growth related proteins including BCL-2, Raf-protein kinase, steroid hormone receptors, growth factor receptors and members of the heat shock protein 70 kDa family. This protein contains a BAG domain near the C-terminus, which could bind and inhibit the chaperone activity of Hsc70/Hsp70. This protein was found to be associated with the death domain of tumor necrosis factor receptor type 1 (TNF-R1) and death receptor-3 (DR3), and thereby negatively regulates downstream cell death signaling. The regulatory role of this protein in cell death was demonstrated in epithelial cells which undergo apoptosis while integrin mediated matrix contacts are lost.[7]

Interactions

BAG4 has been shown to interact with:

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000156735 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000037316 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Takayama S, Xie Z, Reed JC (Feb 1999). "An evolutionarily conserved family of Hsp70/Hsc70 molecular chaperone regulators". J Biol Chem. 274 (2): 781–6. doi:10.1074/jbc.274.2.781. PMID 9873016.
  6. ^ a b Jiang Y, Woronicz JD, Liu W, Goeddel DV (Feb 1999). "Prevention of constitutive TNF receptor 1 signaling by silencer of death domains". Science. 283 (5401): 543–6. Bibcode:1999Sci...283..543J. doi:10.1126/science.283.5401.543. PMID 9915703.
  7. ^ a b "Entrez Gene: BAG4 BCL2-associated athanogene 4".
  8. ^ Lau PP, Chan L (Dec 2003). "Involvement of a chaperone regulator, Bcl2-associated athanogene-4, in apolipoprotein B mRNA editing". J. Biol. Chem. 278 (52): 52988–96. doi:10.1074/jbc.M310153200. PMID 14559896.
  9. ^ a b Miki K, Eddy EM (Apr 2002). "Tumor necrosis factor receptor 1 is an ATPase regulated by silencer of death domain". Mol. Cell. Biol. 22 (8): 2536–43. doi:10.1128/MCB.22.8.2536-2543.2002. PMC 133739. PMID 11909948.

Further reading

  • Riley BM, Schultz RE, Cooper ME, et al. (2007). "A Genome-Wide Linkage Scan for Cleft Lip and Cleft Palate Identifies a Novel Locus on 8p11-23". Am. J. Med. Genet. A. 143 (8): 846–52. doi:10.1002/ajmg.a.31673. PMC 2570349. PMID 17366557.
  • Yang ZQ, Streicher KL, Ray ME, et al. (2007). "Multiple interacting oncogenes on the 8p11-p12 amplicon in human breast cancer". Cancer Res. 66 (24): 11632–43. doi:10.1158/0008-5472.CAN-06-2946. PMID 17178857.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Lau PP, Chan L (2004). "Involvement of a chaperone regulator, Bcl2-associated athanogene-4, in apolipoprotein B mRNA editing". J. Biol. Chem. 278 (52): 52988–96. doi:10.1074/jbc.M310153200. PMID 14559896.
  • Al-Lamki RS, Wang J, Thiru S, et al. (2003). "Expression of Silencer of Death Domains and Death-Receptor-3 in Normal Human Kidney and in Rejecting Renal Transplants". Am. J. Pathol. 163 (2): 401–11. doi:10.1016/S0002-9440(10)63670-X. PMC 1868232. PMID 12875962.
  • Eichholtz-Wirth H, Fritz E, Wolz L (2003). "Overexpression of the 'silencer of death domain', SODD/BAG-4, modulates both TNFR1- and CD95-dependent cell death pathways". Cancer Lett. 194 (1): 81–9. doi:10.1016/S0304-3835(03)00009-0. PMID 12706861.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Briknarová K, Takayama S, Homma S, et al. (2002). "BAG4/SODD protein contains a short BAG domain". J. Biol. Chem. 277 (34): 31172–8. doi:10.1074/jbc.M202792200. PMID 12058034.
  • Eichholtz-Wirth H, Sagan D (2002). "Altered signaling of TNFalpha-TNFR1 and SODD/BAG4 is responsible for radioresistance in human HT-R15 cells". Anticancer Res. 22 (1A): 235–40. PMID 12017295.
  • Antoku K, Maser RS, Scully WJ, et al. (2001). "Isolation of Bcl-2 binding proteins that exhibit homology with BAG-1 and suppressor of death domains protein". Biochem. Biophys. Res. Commun. 286 (5): 1003–10. doi:10.1006/bbrc.2001.5512. PMID 11527400.
  • Frisch SM (2000). "Evidence for a function of death-receptor-related, death-domain-containing proteins in anoikis". Curr. Biol. 9 (18): 1047–9. doi:10.1016/S0960-9822(99)80455-2. PMID 10508612. S2CID 17212216.
  • v
  • t
  • e
  • 1m62: Solution structure of the BAG domain from BAG4/SODD
    1m62: Solution structure of the BAG domain from BAG4/SODD
  • 1m7k: Solution Structure of the SODD BAG Domain
    1m7k: Solution Structure of the SODD BAG Domain


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