Makorin-2 is a neurogenesis inhibitor downstream of phosphatidylinositol 3-kinase/Akt (PI3K/Akt) signal

被引:26
|
作者
Yang, Pai-Hao [1 ,2 ,3 ]
Cheung, William K. C. [1 ]
Peng, Ying [4 ]
He, Ming-Liang [2 ,3 ]
Wu, Guo-Qing [1 ,2 ,3 ]
Xie, Dan [2 ,3 ]
Jiang, Bing-Hua [5 ]
Huang, Qiu-Hua [6 ]
Chen, Zhu [6 ]
Lin, Marie C. M. [1 ]
Kung, Hsiang-Fu [2 ,3 ]
机构
[1] Univ Hong Kong, Dept Chem, Inst Mol Technol, Open Lab Chem Biol, Pokfulam, Hong Kong, Peoples R China
[2] Sun Yat Sen Univ, Joiny State Key Lab Oncol S China, Guangzhou 510120, Peoples R China
[3] Chinese Univ Hong Kong, Shatin, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Neurol, Guangzhou 510120, Peoples R China
[5] Nanjing Med Univ, Dept Pathol, Ctr Canc, Nanjing 210029, Jiangsu, Peoples R China
[6] Shanghai Med Univ 2, Rui Jin Hosp, Shanghai Inst Hematol, Shanghai 200025, Peoples R China
关键词
D O I
10.1074/jbc.M704768200
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
Makorin-2 belongs to the makorin RING zinc finger gene family, which encodes putative ribonucleoproteins. Here we cloned the Xenopus makorin-2 (mkrn2) and characterized its function in Xenopus neurogenesis. Forced overexpression of mkrn2 produced tadpoles with dorso-posterior deficiencies and small-head/short-tail phenotype, whereas knockdown of mkrn2 by morpholino antisense oligonucleotides induced double axis in tadpoles. In Xenopus animal cap explant assay, mkrn2 inhibited activin, and retinoic acid induced animal cap neuralization, as evident from the suppression of a pan neural marker, neural cell adhesion molecule. Surprisingly, the anti-neurogenic activity of mkrn2 is independent of the two major neurogenesis signaling cascades, BMP-4 and Wnt8 pathways. Instead, mkrn2 works specifically through the phosphatidylinositol 3-kinase( PI3K) and Akt-mediated neurogenes is pathway. Overexpression of mkrn2 completely abrogated constitutively active PI3K-and Akt-induced, but not dominant negative glycogen synthase kinase-3 beta(GSK-3 beta)-induced, neural cell adhesion molecule expression, indicating that mkrn2 acts downstream of PI3K and Akt and upstream of GSK-3 beta. Moreover, mkrn2 up-regulated them RNA and protein levels of GSK-3 beta. These results revealed for the first time the important role of mkrn2 as a new player in PI3K/Akt-mediated neurogenesis during Xenopus embryonic development.
引用
收藏
页码:8486 / 8495
页数:10
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