Regulatory feedback loop between TP73 and TRIM32

被引:31
作者
Gonzalez-Cano, L. [1 ]
Hillje, A-L [2 ,3 ]
Fuertes-Alvarez, S. [1 ]
Marques, M. M. [4 ]
Blanch, A. [5 ,6 ]
Ian, R. W. [5 ,6 ]
Irwin, M. S. [5 ,6 ]
Schwamborn, J. C. [2 ,3 ]
Marin, M. C. [1 ]
机构
[1] Univ Leon, Inst Biomed IBIOMED, Dept Mol Biol, E-24071 Leon, Spain
[2] Univ Munster, ZMBE, Inst Cell Biol, Stem Cell Biol & Regenerat Grp, D-48149 Munster, Germany
[3] Univ Luxembourg, LCSB, L-4362 Esch Belval, Luxembourg
[4] Univ Leon, Inst Desarrollo Ganadero, E-24071 Leon, Spain
[5] Univ Toronto, Dept Pediat, Toronto, ON M5G 1X8, Canada
[6] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
p73; TRIM32; ubiquitination; transactivation; E3; ligase; neural differentiation; P73 TRANSCRIPTIONAL ACTIVITY; TUMOR-SUPPRESSOR FUNCTIONS; MOUSE NEURAL PROGENITORS; STEM-CELLS; P53; FAMILY; NEURONAL DIFFERENTIATION; SELF-RENEWAL; PROTEIN; UBIQUITIN; LIGASE;
D O I
10.1038/cddis.2013.224
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The p73 transcription factor is one of the members of the p53 family of tumor suppressors with unique biological functions in processes like neurogenesis, embryonic development and differentiation. For this reason, p73 activity is tightly regulated by multiple mechanisms, including transcription and post-translational modifications. Here, we identified a novel regulatory loop between TAp73 and the E3 ubiquitin ligase tripartite motif protein 32 (TRIM32). TRIM32, a new direct p73 transcriptional target in the context of neural progenitor cells, is differentially regulated by p73. Although TAp73 binds to the TRIM32 promoter and activates its expression, TAp73-induced TRIM32 expression is efficiently repressed by DNp73. TRIM32 in turn physically interacts with TAp73 and promotes its ubiquitination and degradation, impairing p73-dependent transcriptional activity. This mutual regulation between p73 and TRIM32 constitutes a novel feedback loop, which might have important implications in central nervous system development as well as relevance in oncogenesis, and thus emerges as a possible therapeutic target.
引用
收藏
页码:e704 / e704
页数:10
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