Molecular mechanisms of mTOR-mediated translational control

被引:2027
作者
Ma, Xiaoju Max [1 ]
Blenis, John [2 ]
机构
[1] Genentech Inc, Dept Res Oncol Diagnost, San Francisco, CA 94080 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
MESSENGER-RNA TRANSLATION; ACTIVATED PROTEIN-KINASE; INITIATION-FACTOR; 4E; KAPPA-B-KINASE; SPLICING FACTOR SF2/ASF; RICH AKT SUBSTRATE; 40 KDA PRAS40; TUBEROUS-SCLEROSIS; MAMMALIAN TARGET; CELL-GROWTH;
D O I
10.1038/nrm2672
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The process of translation requires substantial cellular resources. Cells have therefore evolved complex mechanisms to control overall protein synthesis as well as the translation of specific mRNAs that are crucial for cell growth and proliferation. At the heart of this process is the mammalian target of rapamycin (mTOR) signalling pathway, which senses and responds to nutrient availability, energy sufficiency, stress, hormones and mitogens to modulate protein synthesis. Here, we highlight recent findings on the regulators and effectors of mTOR and discuss specific cases that serve as paradigms for the different modes of mTOR regulation and its control of translation.
引用
收藏
页码:307 / 318
页数:12
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