BAG3
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). BAG family molecular chaperone regulator 3 is a protein that in humans is encoded by the BAG3 gene. BAG3 is involved in chaperone-assisted selective autophagy.[1][2][3][4][5]
Function
[edit | edit source]BAG proteins compete with Hip-1 for binding to the Hsc70/Hsp70 ATPase domain and promote substrate release. All the BAG proteins have an approximately 45-amino acid BAG domain near the C terminus but differ markedly in their N-terminal regions. The protein encoded by this gene contains a WW domain in the N-terminal region and a BAG domain in the C-terminal region. The BAG domains of BAG1, BAG2, and BAG3 interact specifically with the Hsc70 ATPase domain in vitro and in mammalian cells. All 3 proteins bind with high affinity to the ATPase domain of Hsc70 and inhibit its chaperone activity in a Hip-repressible manner.[3]
Clinical significance
[edit | edit source]BAG gene has been implicated in age related neurodegenerative diseases such as Alzheimer's. It has been demonstrated that BAG1 and BAG3 regulate the proteasomal and lysosomal protein elimination pathways, respectively.[6][7] It has also been shown to be a cause of familial dilated cardiomyopathy.[8] That BAG3 mutations are responsible for familial dilated cardiomyopathy is confirmed by another study describing 6 new molecular variants (2 missense and 4 premature Stops ). Moreover, the same publication reported that BAG3 polymorphisms are also associated with sporadic forms of the disease together with HSPB7 locus.[9]
In muscle cells, BAG3 cooperates with the molecular chaperones Hsc70 and HspB8 to induce the degradation of mechanically damaged cytoskeleton components in lysosomes. This process is called chaperone-assisted selective autophagy and is essential for maintaining muscle activity in flies, mice and men.[4]
BAG3 is able to stimulate the expression of cytoskeleton proteins in response to mechanical tension by activating the transcription regulators YAP1 and WWTR1.[5] BAG3 balances protein synthesis and protein degradation under mechanical stress.
Interactions
[edit | edit source]PLCG1 has been shown to interact with:
- FGFR1,[10]
- CD117,[11][12]
- CD31,[13]
- Cbl gene[14][15]
- CISH[16]
- Epidermal growth factor receptor,[14][17]
- Eukaryotic translation elongation factor 1 alpha 1,[18]
- FLT1,[19]
- GAB1,[20][21]
- GIT1,[22]
- Grb2,[23][24][25]
- HER2/neu,[26][27]
- IRS2,[28]
- ITK,[29][30]
- KHDRBS1,[31][32][33]
- Linker of activated T cells,[34][35][36]
- Lymphocyte cytosolic protein 2,[37]
- PDGFRA,[38]
- PLD2,[39]
- RHOA,[40]
- SOS1,[25][41]
- TUB,[42]
- TrkA,[43][44][45][46]
- TrkB,[45][47]
- VAV1,[48] and
- Wiskott-Aldrich syndrome protein.[49][50]
References
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- ^ Gamerdinger M, Hajieva P, Kaya AM, Wolfrum U, Hartl FU, Behl C. 2009" EMBO J 28(7) 889-901. Protein quality control during aging involves recruitment of the macroautophagy pathway by BAG3
- ^ Physorg:Old Cells Work Differently
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Further reading
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External links
[edit | edit source]- GeneReviews/NIH/NCBI/UW entry on Myofibrillar Myopathy
- Human BAG3 genome location and BAG3 gene details page in the UCSC Genome Browser.
- Overview of all the structural information available in the PDB for UniProt: Q9JLV1 (Mouse BAG family molecular chaperone regulator 3) at the PDBe-KB.