Source:http://linkedlifedata.com/resource/pubmed/id/15499654
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2004-11-1
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pubmed:abstractText |
The function of Aurora-C kinase, a member of the Aurora kinase family identified in mammals, is currently unknown. We present evidence that Aurora-C, like Aurora-B kinase, is a chromosomal passenger protein localizing first to centromeres and then to the midzone of mitotic cells. Aurora-C transcript is expressed at a moderate level albeit about an order of magnitude lower than Aurora-B transcript in diploid human fibroblasts. The level of Aurora-C transcript is elevated in several human cancer cell types. Aurora-C and Aurora-B mRNA and protein expressions are maximally elevated during the G2/M phase but their expression profiles in synchronized cells reveal differential temporal regulation through the cell cycle with Aurora-C level peaking after that of Aurora-B during the later part of the M phase. Aurora-C, like Aurora-B, interacts with the inner centromere protein (INCENP) at the carboxyl terminal end spanning the conserved IN box domain. Competition binding assays and transfection experiments revealed that, compared with Aurora-C, Aurora-B has preferential binding affinity to INCENP and co-expression of the two in vivo interferes with INCENP binding, localization, and stability of these proteins. A kinase-dead mutant of Aurora-C had a dominant negative effect inducing multinucleation in a dose-dependent manner. siRNA mediated silencing of Aurora-C and Aurora-B also gave rise to multinucleated cells with the two kinases silenced at the same time displaying an additive effect. Finally, Aurora-C could rescue the Aurora-B silenced multinucleation phenotype, demonstrating that Aurora-C kinase function overlaps with and complements Aurora-B kinase function in mitosis.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chromosomal Proteins, Non-Histone,
http://linkedlifedata.com/resource/pubmed/chemical/INCENP protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/aurora kinase
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0886-1544
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pubmed:author |
pubmed-author:BrinkleyWilliam RWR,
pubmed-author:EarnshawWilliam CWC,
pubmed-author:FujiiSatoshiS,
pubmed-author:HondaReikoR,
pubmed-author:KatayamaHiroshiH,
pubmed-author:KimuraMasashiM,
pubmed-author:NiggErich AEA,
pubmed-author:OkanoYukioY,
pubmed-author:SasaiKaoriK,
pubmed-author:SenSubrataS,
pubmed-author:StenoienDavid LDL,
pubmed-author:SuzukiFumioF,
pubmed-author:TatsukaMasaakiM
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pubmed:copyrightInfo |
2004 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
59
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
249-63
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pubmed:dateRevised |
2011-7-11
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pubmed:meshHeading |
pubmed-meshheading:15499654-Cell Division,
pubmed-meshheading:15499654-Centromere,
pubmed-meshheading:15499654-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:15499654-Chromosomes, Human,
pubmed-meshheading:15499654-Fibroblasts,
pubmed-meshheading:15499654-G2 Phase,
pubmed-meshheading:15499654-HL-60 Cells,
pubmed-meshheading:15499654-HeLa Cells,
pubmed-meshheading:15499654-Humans,
pubmed-meshheading:15499654-Protein Binding,
pubmed-meshheading:15499654-Protein-Serine-Threonine Kinases,
pubmed-meshheading:15499654-RNA, Small Interfering,
pubmed-meshheading:15499654-Recombinant Proteins,
pubmed-meshheading:15499654-Tumor Cells, Cultured
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pubmed:year |
2004
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pubmed:articleTitle |
Aurora-C kinase is a novel chromosomal passenger protein that can complement Aurora-B kinase function in mitotic cells.
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pubmed:affiliation |
Department of Molecular Pathology, Division of Pathology and Laboratory Medicine, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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