AURKC

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Aurora kinase C
Identifiers
Symbols AURKC ; AIE2; AIK3; AurC; STK13; aurora-C
External IDs Template:OMIM5 HomoloGene68302
RNA expression pattern
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

Aurora kinase C, also known as AURKC, is a human gene.[1]

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.[1]

References

  1. 1.0 1.1 "Entrez Gene: AURKC aurora kinase C".

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.
  • Bernard M, Sanseau P, Henry C; et al. (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. doi:10.1006/geno.1998.5522. PMID 9799611.
  • 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.
  • 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.
  • 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.
  • Clark AG, Glanowski S, Nielsen R; et al. (2003). "Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios". Science. 302 (5652): 1960–3. doi:10.1126/science.1088821. PMID 14671302.
  • Grimwood J, Gordon LA, Olsen A; et al. (2004). "The DNA sequence and biology of human chromosome 19". Nature. 428 (6982): 529–35. doi:10.1038/nature02399. PMID 15057824.
  • 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. doi:10.1074/jbc.M403029200. PMID 15316025.
  • 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. doi:10.1002/cm.20039. PMID 15499654.
  • 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. doi:10.1016/j.bbrc.2004.12.168. PMID 15670791.
  • 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. doi:10.1007/s11373-005-0980-0. PMID 15917996.
  • 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. doi:10.1111/j.1365-2443.2005.00863.x. PMID 15938719.
  • 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.
  • Dieterich K, Soto Rifo R, Faure AK; et al. "Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility". Nat. Genet. 39 (5): 661–5. doi:10.1038/ng2027. PMID 17435757.

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