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CPAP interacts with 14-3-3 in a cell cycle-dependent manner
被引:9
作者:
Chen, CY
Olayioye, MA
Lindeman, GJ
Tang, TK
[1
]
机构:
[1] Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei 114, Taiwan
[3] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
关键词:
centrosome;
CPAP;
14-3-3;
cell cycle;
protein;
4.1;
phosphorylation;
D O I:
10.1016/j.bbrc.2006.02.089
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
We have previously reported that CPAP (Centrosomal Protein 4.1-Associated Protein) carries a novel microtubule-destabilizing motif that may regulate microtubule dynamics at the centrosome. In this study, we searched for conserved sequence motifs in CPAP and identified two classical 14-3-3 binding sites. The interaction between CPAP and 14-3-3 was demonstrated by both yeast two-hybrid and co-immunoprecipitation experiments. Further analyses revealed that the 14-3-3 binding motif is located within the C-terminal domain of CPAP. Alkaline phosphatase treatment disrupted CPAP binding to 14-3-3, Suggesting that phosphorylation is required for the interaction. Mutation of serine 1109 to alanine (S1 109A) in the 14-3-3 binding motif completely abolished the association of CPAP with 14-3-3. Taking together, these results imply that phosphorylation of CPAP on serine 1109 is required for 14-3-3 binding. Furthermore, we observed that the interaction between CPAP and 14-3-3 was significantly reduced in mitotic cells. suggesting that 14-3-3 binding to CPAP is regulated during cell cycle progression. In Summary, Our results show a direct interaction between CPAP and 14-3-3, and this interaction appears to be phosphorylation and cell cycle dependent. (c) 2006 Elsevier Inc. All rights reserved.
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页码:1203 / 1210
页数:8
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