共 6 条
Activation/Proliferation-associated Protein 2 (Caprin-2) Positively Regulates CDK14/Cyclin Y-mediated Lipoprotein Receptor-related Protein 5 and 6 (LRP5/6) Constitutive Phosphorylation
被引:18
|作者:
Wang, Xin
[1
]
Jia, Yingying
[1
]
Fei, Cong
[1
]
Song, Xiaomin
[1
]
Li, Lin
[1
]
机构:
[1] Chinese Acad Sci, Ctr Excellence Mol Cell Sci, Innovat Ctr Cell Signaling Network, State Key Lab Mol Biol,Inst Biochem & Cell Biol,S, Shanghai 200031, Peoples R China
基金:
中国国家自然科学基金;
关键词:
CELL-CYCLE CONTROL;
LRP6;
PHOSPHORYLATION;
BETA-CATENIN;
WNT PATHWAY;
STEM-CELLS;
IDENTIFICATION;
ACTIVATION;
EXPRESSION;
STABILIZATION;
DROSOPHILA;
D O I:
10.1074/jbc.M116.744607
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:
Low-density lipoprotein receptor-related proteins 5 and 6 (LRP5/6) are co-receptors for Wnt ligands. Upon ligand binding, LRP5/6 undergo glycogen synthase kinase 3 (GSK3)/casein kinase I (CKI)-mediated phosphorylation at multiple PPP(S/T) P motifs in the intracellular domain, which is essential for canonical Wnt signal transduction. On the other hand, in the Wnt-off state, the mitosis-specific CDK14-Cyclin Y kinase complex phosphorylates Ser-1490 of LRP5/6 at G(2)/M, thereby priming the receptor for Wnt-induced phosphorylation. However, it remains unclear how CDK14/Cyclin Y is recruited to LRP5/6 and whether there are other cofactors involved in this process. Previously, we identified Caprin-2 as a positive regulator of canonical Wnt signaling by promoting GSK3-depedent LRP5/6 phosphorylation upon Wnt stimulation. Here we uncovered that Caprin-2 positively regulates constitutive LRP5/6 Ser-1490 phosphorylation by complexing with CDK14/Cyclin Y. Caprin-2-mediated LRP5/6 phosphorylation is cell cycle-dependent in a pattern similar to that of CDK14/Cyclin Y-dependent LRP5/6 phosphorylation. Moreover, knockdown of Caprin-2 disrupts not only the interaction between CDK14 and Cyclin Y but also the interaction between CDK14/Cyclin Y and LRP6. Overall, our findings revealed an unrecognized role of Caprin-2 in facilitating LRP5/6 constitutive phosphorylation at G(2)/M through forming a quaternary complex with CDK14, Cyclin Y, and LRP5/6.
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页码:26427 / 26434
页数:8
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