Regulation and function of ribosomal protein S6 kinase (S6K) within mTOR signalling networks

被引:783
作者
Magnuson, Brian [1 ]
Ekim, Bilgen [1 ]
Fingar, Diane C. [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Div Metab Endocrinol & Diabet, Dept Med, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
mammalian target of rapamycin complex 1 (mTORC1); mammalian target of rapamycin complex 2 (mTORC2); S6 kinase 1 (S6K1); S6 kinase 2 (S6K2); target of rapamycin (TOR); TOP MESSENGER-RNAS; HYDROPHOBIC MOTIF PHOSPHORYLATION; IKK-BETA SUPPRESSION; IN-VIVO ROLE; MAMMALIAN TARGET; CELL-GROWTH; TUBEROUS SCLEROSIS; RAPAMYCIN MTOR; KAPPA-B; TRANSLATION INITIATION;
D O I
10.1042/BJ20110892
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
The ribosomal protein S6K (S6 kinase) represents an extensively studied effector of the TORC1 [TOR (target of rapamycin) complex 1]. which possesses important yet incompletely defined roles in cellular and organismal physiology. TORC1 functions as an environmental sensor by integrating signals derived from diverse environmental cues to promote anabolic and inhibit catabolic cellular functions. mTORC1 (mammalian TORC1) phosphorylates and activates S6K1 and S6K2, whose first identified substrate was rpS6 (ribosomal protein S6), a component of the 40S ribosome. Studies over the past decade have uncovered a number of additional S6K1 substrates, revealing multiple levels at which the mTORC1-S6K1 axis regulates cell physiology. The results thus far indicate that the mTORC1-S6K1 axis controls fundamental cellular processes, including transcription, translation, protein and lipid synthesis, cell growth/size and cell metabolism. In the present review we summarize the regulation of S6Ks, their cellular substrates and functions, and their integration within rapidly expanding mTOR (mammalian TOR) signalling networks. Although our understanding of the role of mTORC1-S6K1 I signalling in physiology remains in its infancy, evidence indicates that this signalling axis controls, at least in part, glucose homoeostasis, insulin sensitivity, adipocyte metabolism, body mass and energy balance, tissue and organ size, learning, memory and aging. As dysregulation of this signalling axis contributes to diverse disease states, improved understanding of S6K regulation and function within mTOR signalling networks may enable the development of novel therapeutics.
引用
收藏
页码:1 / 21
页数:21
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