MDM2 interacts with and downregulates a sarcomeric protein, TCAP

被引:41
|
作者
Tian, Li-Feng [1 ]
Li, Hui-Yan [1 ]
Jin, Bao-Feng [1 ]
Pan, Xin [1 ]
Man, Jiang-Hong [1 ]
Zhang, Pei-Jing [1 ]
Li, Wei-Hua [1 ]
Liang, Bing [1 ]
Liu, Hui [1 ]
Zhao, He [1 ]
Gong, Wei-Li [1 ]
Zhou, Tao [1 ]
Zhang, Xue-Min [1 ]
机构
[1] Natl Ctr Biomed Anal, Beijing 100850, Peoples R China
基金
中国国家自然科学基金;
关键词
MDM2; interaction; TCAP; p14(ARF); degradation; yeast two-hybrid screen; cardiac hypertrophy; UBIQUITIN LIGASE ACTIVITY; BETA-CATENIN; G(1) ARREST; P53; PROTEIN; DEGRADATION; PROMOTES; TELETHONIN; MUTATIONS; STABILITY; APOPTOSIS;
D O I
10.1016/j.bbrc.2006.04.108
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
Recent reports have shown that MDM2 may attenuate hypertrophy of cardiac myocytes. However, mechanism of MDM2 involving in this process is unclear. In this study, we identified a novel specific MDM2-binding protein TCAP by the yeast two-hybrid screen. It was validated by GST pull-down and co-immunoprecipitation assays. Confocal analysis showed that MDM2 and TCAP co-localized in the nucleus, and elevated MDM2 expression could alter the subcellular localization of TCAP. Notably, MDM2 downregulated the protein level of TCAP through the proteasomal pathway, and this downregulation was inhibited by p14(ARF). In addition, our results suggested that the degradation of TCAP by MDM2 was through the ubiquitin-independent pathway. Given that TCAP is a key component involving in the cardiac hypertrophy, the degradation of TCAP by MDM2 might be connected with the roles of MDM2 in cardiac hypertrophy. Further investigation will focus on the biological significance of MDM2-TCAP interaction in cardiac hypertrophy. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:355 / 361
页数:7
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