eIF4在细胞增殖中的作用。

Cancer surveys Pub Date : 1996-01-01
A Flynn, C G Proud
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引用次数: 0

摘要

翻译控制在调节细胞生长中起着关键作用。mRNA结合翻译因子(mRNA binding translation factors, eIF4s)根据不同mRNA的特性,特别是其5'非翻译区抑制二级结构的程度,选择性地调节不同mRNA的翻译。mRNA 5'帽被eIF4E识别,然后eIF4E可以招募其他翻译因子,包括解旋酶cIF4A。过表达eIF4E可导致细胞转化或生长紊乱。它还增强了某些mrna的翻译,包括cyclin D1的翻译。eIF4E表达降低导致细胞生长速率降低。转化细胞表达高水平的eIF4E。eIF4E受磷酸化影响,刺激翻译的药物会增加磷酸化。然而,eIF4E磷酸化的作用及其控制的信号通路仍有待阐明。致癌ras导致eIF4E磷酸化增加,当eIF4E表达降低时,ras转化细胞的能力减弱,这意味着eIF4E是ras介导转化的关键介质。最近发现的eIF4E抑制剂(eIF4E结合蛋白,4EBP1/2)为该系统增加了另一个调节成分。尽管4EBP1在细胞转化(或者更确切地说是阻碍细胞转化)中的作用尚未确定,但这是一个令人兴奋和可能的可能性。还应注意的是,4EBP1似乎受p70S6K通路的控制,p70S6K通路在细胞周期进程中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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The role of eIF4 in cell proliferation.

Translational control has a key role in regulating cell growth. The mRNA binding translation factors (eIF4s) selectively modulate the translation of different mRNAs based on their differing properties, especially the extent of inhibitory secondary structure in their 5' untranslated regions. The mRNA 5' cap is recognized by eIF4E, which can then recruit other translation factors including the helicase cIF4A. Overexpression of eIF4E leads to cell transformation or disordered growth. It also enhances the translation of certain mRNAs, including that for cyclin D1. Decreased expression of eIF4E leads to reduced rates of cell growth. Transformed cells express elevated levels of eIF4E. eIF4E is subject to phosphorylation, which is increased by agents that stimulate translation. However, the role of eIF4E phosphorylation and the signalling pathways through which it is controlled remain to be elucidated. Oncogenic ras leads to increased phosphorylation of eIF4E, and the ability of ras to transform cells is diminished when eIF4E expression is decreased, implying that eIF4E is a key mediator of ras mediated transformation. The recent discovery of inhibitors of eIF4E (eIF4E binding proteins, 4EBP1/2) adds another regulatory component to the system. Although a role for 4EBP1 in cell transformation (or rather in impeding it) has yet to be established, this is an exciting and likely possibility. It should also be noted that 4EBP1 seems to be under the control of the p70S6K pathway, which has a role in cell cycle progression.

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