Identification of extracellular signal-regulated kinase 3 as a new interaction partner of cyclin D3

被引:16
|
作者
Sun, MY
Wei, YY
Yao, LY
Xie, JH
Chen, XN
Wang, HZ
Jiang, JH
Gu, JX [1 ]
机构
[1] Fudan Univ, Shanghai Med Coll, State Key Lab Genet Engn, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Ctr Gene Res, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
cyclin D3; ERK3; yeast two-hybrid; protein interaction;
D O I
10.1016/j.bbrc.2005.12.003
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
Cyclin D3, like cyclin D1 and D2 isoforms, is a crucial component of the core cell cycle machinery in mammalian cells. It also exhibits its unique properties in many other physiological processes. In the present study, using yeast two-hybrid screening, we identified ERK3, an atypical mitogen-activated protein kinase (MAPK), as a cyclin D3 binding partner. GST pull-down assays showed that cyclin D3 interacts directly and specifically with ERK3 in vitro. The binding of cyclin D3 and ERK3 was further confirmed in vivo by co-immunoprecipitation assay and confocal microscopic analysis. Moreover, carboxy-terminal extension of ERK3 was responsible for its association with intact cyclin D3. These findings further expand distinct roles of cyclin D3 and suggest the potential activity of ERK3 in cell proliferation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:209 / 214
页数:6
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