Translational Homeostasis via the mRNA Cap-Binding Protein, elF4E

被引:137
作者
Yanagiya, Akiko [1 ,2 ]
Suyama, Eigo [3 ]
Adachi, Hironori [1 ,2 ]
Svitkin, Yuri V. [1 ,2 ]
Aza-Blanc, Pedro [3 ]
Imataka, Hiroaki [5 ]
Mikami, Satoshi [6 ]
Martineau, Yvan [1 ,2 ]
Ronai, Ze'ev A. [4 ]
Sonenberg, Nahum [1 ,2 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3A 1A3, Canada
[2] McGill Univ, McGill Canc Ctr, Montreal, PQ H3A 1A3, Canada
[3] Sanford Burnham Med Res Inst, Funct Genom Core, La Jolla, CA 92037 USA
[4] Sanford Burnham Med Res Inst, Signal Transduct Program, La Jolla, CA 92037 USA
[5] Univ Hyogo, Grad Sch Engn, Dept Mat Sci & Chem, Himeji, Hyogo 6712280, Japan
[6] RIKEN Syst & Struct Biol Ctr, Yokohama, Kanagawa 2300045, Japan
基金
加拿大健康研究院; 日本学术振兴会;
关键词
INITIATION-FACTOR; 4E; PHOSPHORYLATION; INHIBITOR; UBIQUITINATION; DEGRADATION; EXPRESSION; STABILITY; RIBOSOME; ADAPTERS; INSULIN;
D O I
10.1016/j.molcel.2012.04.004
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
Translational control of gene expression plays a key role in many biological processes. Consequently, the activity of the translation apparatus is under tight homeostatic control. elF4E, the mRNA 5' cap-binding protein, facilitates cap-dependent translation and is a major target for translational control. elF4E activity is controlled by a family of repressor proteins, termed 4E-binding proteins (4E-BPs). Here, we describe the surprising finding that despite the importance of elF4E for translation, a drastic knockdown of elF4E caused only minor reduction in translation. This conundrum can be explained by the finding that 4E-BP1 is degraded in elF4E-knock-down cells. Hypophosphorylated 4E-BP1, which binds to elF4E, is degraded, whereas hyperphosphorylated 4E-BP1 is refractory to degradation. We identified the KLHL25-CUL3 complex as the E3 ubiquitin ligase, which targets hypophosphorylated 4E-BP1. Thus, the activity of elF4E is under homeostatic control via the regulation of the levels of its repressor protein 4E-BP1 through ubiquitination.
引用
收藏
页码:847 / 858
页数:12
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