FASTK

From Wikipedia, the free encyclopedia


Fas-activated serine/threonine kinase
Identifiers
Symbol(s) FASTK; FAST
External IDs OMIM: 606965 MGI1913837 HomoloGene4884
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 10922 66587
Ensembl ENSG00000164896 n/a
Uniprot Q14296 n/a
Refseq NM_006712 (mRNA)
NP_006703 (protein)
XM_982275 (mRNA)
XP_987369 (protein)
Location Chr 7: 150.4 - 150.41 Mb n/a
Pubmed search [1] [2]

Fas-activated serine/threonine kinase, also known as FASTK, is a human gene.[1]

The protein encoded by this gene is a member of the serine/threonine protein kinase family. This kinase was shown to be activated rapidly during Fas-mediated apoptosis in Jurkat cells. In response to Fas receptor ligation, it phosphorylates TIA1, an apoptosis-promoting nuclear RNA-binding protein. The encoded protein is a strong inducer of lymphocyte apoptosis. Two transcript variants encoding different isoforms have been found for this gene. Other variants exist, but their full-length natures have not yet been determined.[1]

[edit] References

[edit] Further reading

  • Tian Q, Taupin J, Elledge S, et al. (1995). "Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosis.". J. Exp. Med. 182 (3): 865–74. PMID 7544399. 
  • Auffray C, Behar G, Bois F, et al. (1995). "[IMAGE: molecular integration of the analysis of the human genome and its expression]". C. R. Acad. Sci. III, Sci. Vie 318 (2): 263–72. PMID 7757816. 
  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171–4. PMID 8125298. 
  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791–806. PMID 8889548. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149–56. PMID 9373149. 
  • 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. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Scherer SW, Cheung J, MacDonald JR, et al. (2003). "Human chromosome 7: DNA sequence and biology.". Science 300 (5620): 767–72. doi:10.1126/science.1083423. PMID 12690205. 
  • 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. 
  • Li W, Kedersha N, Chen S, et al. (2004). "FAST is a BCL-X(L)-associated mitochondrial protein.". Biochem. Biophys. Res. Commun. 318 (1): 95–102. doi:10.1016/j.bbrc.2004.03.188. PMID 15110758. 
  • 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. PMID 15489334. 
  • Li W, Simarro M, Kedersha N, Anderson P (2004). "FAST is a survival protein that senses mitochondrial stress and modulates TIA-1-regulated changes in protein expression.". Mol. Cell. Biol. 24 (24): 10718–32. doi:10.1128/MCB.24.24.10718-10732.2004. PMID 15572676. 
  • 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. doi:10.1038/nature04209. PMID 16189514. 
  • Oh JH, Yang JO, Hahn Y, et al. (2006). "Transcriptome analysis of human gastric cancer.". Mamm. Genome 16 (12): 942–54. doi:10.1007/s00335-005-0075-2. PMID 16341674. 
  • Izquierdo JM, Valcárcel J (2007). "Fas-activated serine/threonine kinase (FAST K) synergizes with TIA-1/TIAR proteins to regulate Fas alternative splicing.". J. Biol. Chem. 282 (3): 1539–43. doi:10.1074/jbc.C600198200. PMID 17135269. 
  • Simarro M, Mauger D, Rhee K, et al. (2007). "Fas-activated serine/threonine phosphoprotein (FAST) is a regulator of alternative splicing.". Proc. Natl. Acad. Sci. U.S.A. 104 (27): 11370–5. doi:10.1073/pnas.0704964104. PMID 17592127.