Insulin/TOR signaling in growth and homeostasis: A view from the fly world

被引:175
作者
Grewal, Savraj S. [1 ,2 ]
机构
[1] Univ Calgary, So Alberta Canc Res Inst, Dept Biochem & Mol Biol, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Dept Oncol, Calgary, AB T2N 4N1, Canada
关键词
Insulin; PI3; kinase; TOR; Cell growth; Ribosome synthesis; Translation; Autophagy; Endocytosis; CELL-GROWTH; LIFE-SPAN; TRANSCRIPTIONAL RESPONSE; DROSOPHILA-MELANOGASTER; CAENORHABDITIS-ELEGANS; STRESS RESISTANCE; OXIDATIVE STRESS; FAT-BODY; TOR; PATHWAY;
D O I
10.1016/j.biocel.2008.10.010
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 insulin/TOR pathway is a conserved regulator of cell and organism growth in metazoans. Over the last several years, an array of signaling inputs to this pathway has been defined. However the growth-regulatory outputs are less clear. Drosophila has proven to be a powerful genetic model system in which to study insulin[TOR signaling. This review highlights recent studies in Drosophila that have identified essential outputs and key effectors of the pathway. These include the regulation of ribosome synthesis, mRNA translation, autophagy and endocytosis, through downstream effectors such as Myc, FOXO, HIF1-alpha, TIF-1A, 4EBP and Atg1. This network of outputs and effectors can regulate cell and organismal metabolism, and is essential for the control of tissue growth, responses to starvation and stress, and aging. The mechanisms identified in Drosophila likely operate in most metazoans, and are relevent to our understanding of diseases caused by aberrent insulin/TOR signaling such as cancer, diabetes and obesity. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1006 / 1010
页数:5
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