AURKC
Serine/threonine-protein kinase 13 is an enzyme that in humans is encoded by the AURKC gene.[3][4]
This gene encodes a member of the Aurora subfamily of serine/threonine protein kinases. The encoded protein is a chromosomal passenger protein that forms complexes with Aurora-B and inner centromere proteins and may play a role in organizing microtubules in relation to centrosome/spindle function during mitosis. This gene is overexpressed in several cancer cell lines, suggesting an involvement in oncogenic signal transduction. Alternative splicing results in multiple transcript variants.[4]
References
- ↑ "Human PubMed Reference:".
- ↑ "Mouse PubMed Reference:".
- ↑ Bernard M, Sanseau P, Henry C, Couturier A, Prigent C (Dec 1998). "Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipl1 that maps on chromosome 19q13.3-ter". Genomics. 53 (3): 406–9. PMID 9799611. doi:10.1006/geno.1998.5522.
- 1 2 "Entrez Gene: AURKC aurora kinase C".
External links
- Human AURKC genome location and AURKC gene details page in the UCSC Genome Browser.
Further reading
- Katayama H, Brinkley WR, Sen S (2004). "The Aurora kinases: role in cell transformation and tumorigenesis.". Cancer Metastasis Rev. 22 (4): 451–64. PMID 12884918. doi:10.1023/A:1023789416385.
- Tseng TC, Chen SH, Hsu YP, Tang TK (1998). "Protein kinase profile of sperm and eggs: cloning and characterization of two novel testis-specific protein kinases (AIE1, AIE2) related to yeast and fly chromosome segregation regulators.". DNA Cell Biol. 17 (10): 823–33. PMID 9809744. doi:10.1089/dna.1998.17.823.
- Kimura M, Matsuda Y, Yoshioka T, Okano Y (1999). "Cell cycle-dependent expression and centrosome localization of a third human aurora/Ipl1-related protein kinase, AIK3.". J. Biol. Chem. 274 (11): 7334–40. PMID 10066797. doi:10.1074/jbc.274.11.7334.
- 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. PMC 139241 . PMID 12477932. doi:10.1073/pnas.242603899.
- Clark AG, Glanowski S, Nielsen R, et al. (2003). "Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios.". Science. 302 (5652): 1960–3. PMID 14671302. doi:10.1126/science.1088821.
- Grimwood J, Gordon LA, Olsen A, et al. (2004). "The DNA sequence and biology of human chromosome 19.". Nature. 428 (6982): 529–35. PMID 15057824. doi:10.1038/nature02399.
- Li X, Sakashita G, Matsuzaki H, et al. (2004). "Direct association with inner centromere protein (INCENP) activates the novel chromosomal passenger protein, Aurora-C.". J. Biol. Chem. 279 (45): 47201–11. PMID 15316025. doi:10.1074/jbc.M403029200.
- Sasai K, Katayama H, Stenoien DL, et al. (2005). "Aurora-C kinase is a novel chromosomal passenger protein that can complement Aurora-B kinase function in mitotic cells.". Cell Motil. Cytoskeleton. 59 (4): 249–63. PMID 15499654. doi:10.1002/cm.20039.
- Yan X, Wu Y, Li Q, et al. (2005). "Cloning and characterization of a novel human Aurora C splicing variant.". Biochem. Biophys. Res. Commun. 328 (1): 353–61. PMID 15670791. doi:10.1016/j.bbrc.2004.12.168.
- Chen HL, Tang CJ, Chen CY, Tang TK (2005). "Overexpression of an Aurora-C kinase-deficient mutant disrupts the Aurora-B/INCENP complex and induces polyploidy.". J. Biomed. Sci. 12 (2): 297–310. PMID 15917996. doi:10.1007/s11373-005-0980-0.
- Yan X, Cao L, Li Q, et al. (2005). "Aurora C is directly associated with Survivin and required for cytokinesis.". Genes Cells. 10 (6): 617–26. PMID 15938719. doi:10.1111/j.1365-2443.2005.00863.x.
- Dutertre S, Hamard-Péron E, Cremet JY, et al. (2006). "The absence of p53 aggravates polyploidy and centrosome number abnormality induced by Aurora-C overexpression.". Cell Cycle. 4 (12): 1783–7. PMID 16258285. doi:10.4161/cc.4.12.2172.
- Dieterich K, Soto Rifo R, Faure AK, et al. (2007). "Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility.". Nat. Genet. 39 (5): 661–5. PMID 17435757. doi:10.1038/ng2027.
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