TBCE

TBCE
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4ICU, 4ICV
Identifiers
Aliases	TBCE , HRD, KCS, KCS1, pac2, tubulin folding cofactor E, PEAMO
External IDs	OMIM: 604934 MGI: 1917680 HomoloGene: 37744 GeneCards: TBCE
Gene location (Mouse) Chr. Chromosome 13 (mouse) [1] Band 13 A1|13 5.29 cM Start 14,172,534 bp [1] End 14,214,223 bp [1]
RNA expression pattern Bgee Human Mouse (ortholog) n/a Top expressed in superior frontal gyrus cerebellar cortex spermatid neural tube ganglionic eminence mirror thymus saccule facial motor nucleus lip BioGPS More reference expression data
Gene ontology Molecular function chaperone binding protein binding alpha-tubulin binding Cellular component cytoplasm microtubule cytoskeleton Biological process post-chaperonin tubulin folding pathway protein folding mitotic spindle organization microtubule cytoskeleton organization tubulin complex assembly Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 6905 70430 Ensembl ENSG00000116957 ENSMUSG00000039233 UniProt Q15813 Q8CIV8 RefSeq (mRNA) NM_003193 NM_001079515 NM_001287801 NM_001287802 NM_178337 RefSeq (protein) NP_001072983 NP_001274730 NP_001274731 NP_003184 NP_848027 Location (UCSC) n/a Chr 13: 14.17 – 14.21 Mb PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Tubulin-specific chaperone E is a protein that in humans is encoded by the TBCE gene. ^{[4] [5]}

Cofactor E is one of four proteins (cofactors A, D, E, and C) involved in the pathway leading to correctly folded beta-tubulin from folding intermediates. Cofactors A and D are believed to play a role in capturing and stabilizing beta-tubulin intermediates in a quasi-native confirmation. Cofactor E binds to the cofactor D/beta-tubulin complex; interaction with cofactor C then causes the release of beta-tubulin polypeptides that are committed to the native state. Two transcript variants encoding the same protein have been found for this gene. ^[5]

The TBCE gene is either deleted or mutated in Sanjad-Sakati Syndrome

References

1. GRCm38: Ensembl release 89: ENSMUSG00000039233 - Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. Tian G, Huang Y, Rommelaere H, Vandekerckhove J, Ampe C, Cowan NJ (Sep 1996). "Pathway leading to correctly folded beta-tubulin". Cell. 86 (2): 287–96. doi: 10.1016/S0092-8674(00)80100-2 . PMID   8706133. S2CID   18359371.
5. "Entrez Gene: TBCE tubulin folding cofactor E".

Further reading

• Lewis SA, Tian G, Vainberg IE, Cowan NJ (1996). "Chaperonin-mediated folding of actin and tubulin". J. Cell Biol. 132 (1–2): 1–4. doi:10.1083/jcb.132.1.1. PMC   2120700 . PMID   8567715.
• Parvari R, Diaz GA, Hershkovitz E (2007). "Parathyroid development and the role of tubulin chaperone E". Horm. Res. 67 (1): 12–21. doi: 10.1159/000095944 . PMID   17008776.
• Tian G, Lewis SA, Feierbach B, et al. (1997). "Tubulin subunits exist in an activated conformational state generated and maintained by protein cofactors". J. Cell Biol. 138 (4): 821–32. doi:10.1083/jcb.138.4.821. PMC   2138046 . PMID   9265649.
• Parvari R, Hershkovitz E, Kanis A, et al. (1998). "Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43". Am. J. Hum. Genet. 63 (1): 163–9. doi:10.1086/301915. PMC   1377236 . PMID   9634513.
• Diaz GA, Khan KT, Gelb BD (1999). "The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43". Genomics. 54 (1): 13–8. doi:10.1006/geno.1998.5530. PMID   9806825.
• Roobol A, Sahyoun ZP, Carden MJ (1999). "Selected subunits of the cytosolic chaperonin associate with microtubules assembled in vitro". J. Biol. Chem. 274 (4): 2408–15. doi: 10.1074/jbc.274.4.2408 . PMID   9891010.
• Parvari R, Hershkovitz E, Grossman N, et al. (2002). "Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome". Nat. Genet. 32 (3): 448–52. doi:10.1038/ng1012. PMID   12389028. S2CID   23979186.
• Martin N, Jaubert J, Gounon P, et al. (2002). "A missense mutation in Tbce causes progressive motor neuronopathy in mice". Nat. Genet. 32 (3): 443–7. doi:10.1038/ng1016. PMID   12389029. S2CID   7279049.
• Bommel H, Xie G, Rossoll W, et al. (2003). "Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease". J. Cell Biol. 159 (4): 563–9. doi:10.1083/jcb.200208001. PMC   2173089 . PMID   12446740.
• 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.
• Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID   12665801. S2CID   23783563.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi: 10.1038/ng1285 . PMID   14702039.
• 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.
• Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID   16189514. S2CID   4427026.
• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC   1356129 . PMID   16344560.
• Gregory SG, Barlow KF, McLay KE, et al. (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. 441 (7091): 315–21. Bibcode:2006Natur.441..315G. doi: 10.1038/nature04727 . PMID   16710414.
• Kortazar D, Fanarraga ML, Carranza G, et al. (2007). "Role of cofactors B (TBCB) and E (TBCE) in tubulin heterodimer dissociation". Exp. Cell Res. 313 (3): 425–36. doi:10.1016/j.yexcr.2006.09.002. PMID   17184771.