TRIB1

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TRIB1
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases TRIB1, C8FW, GIG-2, GIG2, SKIP1, TRB-1, TRB1, tribbles pseudokinase 1
External IDs MGI: 2443397 HomoloGene: 75216 GeneCards: TRIB1
RNA expression pattern
PBB GE TRIB1 202241 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001282985
NM_025195

NM_144549

RefSeq (protein)

NP_001269914
NP_079471

NP_653132

Location (UCSC) Chr 8: 125.43 – 125.44 Mb Chr 15: 59.65 – 59.66 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Tribbles homolog 1 is a protein kinase that in humans is encoded by the TRIB1 gene.[3][4][5] Orthologs of this protein pseudokinase (pseudoenzyme) can be found almost ubiquitously throughout the animal kingdom.[6] It exerts its biological functions through binding to signalling proteins of the MAPKK level of the MAPK pathway, therefore eliciting a regulatory role in the function of this pathway which mediates proliferation, apoptosis and differentiation in cells. Tribbles-1 is encoded by the trib1 gene, which in humans can be found on chromosome 8 at position 24.13 on the longest arm (q). Recent crystal structures show that Tribbles 1 has an unusual 3D structure, containing a 'broken' C-helix region, a binding site for ubiquitinated substrates such as C/EBPalpha and a key regulatory C-tail region.[7] Like TRIB2 and TRIB3, TRIB1 has recently been considered as a potential allosteric drug target [8]

Function[edit]

Tribbles-1 is one of three members of the Tribbles subfamily, which is a part of the CAMK Ser/Thr protein kinase family, of the protein kinase superfamily. The Tribbles subfamily is one of the pseudokinases, meaning that while expressing putative kinase regions in its structure, it is non-catalytic. The Tribbles subfamily lacks a functional ATP binding pocket, and therefore cannot phosphorylate its substrates; instead, Tribbles proteins function as scaffold proteins, which bind their substrates to localize them to or from their function [6]

Expression of Tribbles-1 is highly variable, constantly changing with respect to time and cell-type,[9] which suggests a large amount of regulation that exists in the cell. The protein's primary structure contains a PEST region, indicative of proteins that are highly susceptible to degradation in the cell; Tribbles-1 plays a role in regulating its own expression by binding to its substrate, which not only produces its function on the MAPK pathway, but also works to protect it from degradation whilst binding. This, in part, creates a positive feedback loop in the function of Tribbles-1, as the function of Tribbles-1 directly aids in the increase of the amount of it. As positive feedback loops are often seen throughout biology in circumstances that require the alleviation of an external stimulus, the positive feedback loop exhibited by Tribbles-1 suggests that it plays a functional role in cell response.

Clinical significance[edit]

Tribbles-1 is an inflammatory regulator.

Tribbles-1 is associated with Acute Myeloid Leukemia (AML).

Tribbles-1 has been implicated in atherosclerosis.

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ Wilkin F; Suarez-Huerta N; Robaye B; Peetermans J; Libert F; Dumont JE; Maenhaut C (Nov 1997). "Characterization of a phosphoprotein whose mRNA is regulated by the mitogenic pathways in dog thyroid cells". Eur J Biochem. 248 (3): 660–68. PMID 9342215. doi:10.1111/j.1432-1033.1997.t01-1-00660.x. 
  4. ^ Hegedus Z, Czibula A, Kiss-Toth E (Aug 2006). "Tribbles: novel regulators of cell function; evolutionary aspects". Cell Mol Life Sci. 63 (14): 1632–41. PMID 16715410. doi:10.1007/s00018-006-6007-9. 
  5. ^ "Entrez Gene: TRIB1 tribbles homolog 1 (Drosophila)". 
  6. ^ a b Eyers PA, Keeshan K, Kannan N (2016). "Tribbles in the 21st Century: The Evolving Roles of Tribbles Pseudokinases in Biology and Disease.". Trends in Cell Biology. In Press (9): S0962–8924(16)30178–7. PMID 27908682. doi:10.1016/j.tcb.2016.11.002. 
  7. ^ Eyers PA, Keeshan K, Kannan N (2015). "Molecular Mechanism of CCAAT-Enhancer Binding Protein Recruitment by the TRIB1 Pseudokinase.". Structure. 23 (11): 2111–2121. PMID 26455797. doi:10.1016/j.str.2015.08.017. 
  8. ^ Foulkes DM, Byrne DP, Eyers PA (2015). "Tribbles pseudokinases: novel targets for chemical biology and drug discovery?". Biochem Soc Transactions. 43 (5): 1095–1103. PMID 26517930. doi:10.1042/BST20150109. 
  9. ^ Sung HY, Francis SE, Crossman DC, Kiss-Toth E (Apr 2006). "Regulation of expression and signalling modulator function of mammalian tribbles is cell-type specific". Immunology Lett. 104 (1-2): 171–177. PMID 16364454. doi:10.1016/j.imlet.2005.11.010. 

Further reading[edit]

External links[edit]