The life cycle of C-myc - From synthesis to degradation

被引:303
作者
Sears, RC [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Mol & Med Genet, Portland, OR 97239 USA
关键词
c-Myc; Ras; ERK; GSK-3; beta; Pin1; PP2A; Threonine; 58; Serine; 62; stability;
D O I
10.4161/cc.3.9.1145
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The c-Myc transcription factor is a potent regulator of cellular proliferation and cell fate decision. Precise regulation of c-Myc protein levels is essential to maintain normal cell function. In order to maintain proper levels of c-Myc, its protein stability is tightly controlled. c-Myc is degraded through the ubiquitin-proteasome pathway. This perspective discusses a sophisticated and complex signaling pathway that controls the life cycle of c-Myc from protein synthesis to ubiquitin-mediated degradation. The pathway involves Ras-activated kinases, the Pin1 prolyl isomerase, the PP2A phosphatase and a series of c-Myc phosphorylation and dephosphorylation events that control its stability.
引用
收藏
页码:1133 / 1137
页数:5
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