Regulation of FoxO transcription factors by acetylation and protein-protein interactions

被引:225
作者
Daitoku, Hiroaki [1 ]
Sakamaki, Jun-ichi [1 ]
Fukamizu, Akiyoshi [1 ]
机构
[1] Univ Tsukuba, Life Sci Ctr, Tsukuba, Ibaraki 3058577, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2011年 / 1813卷 / 11期
关键词
FoxO; Acetylation; Protein-protein interactions; FORKHEAD TRANSCRIPTION; OXIDATIVE STRESS; FOXO1-MEDIATED TRANSCRIPTION; FUNCTIONAL INTERACTION; BETA-CATENIN; DNA-BINDING; LIFE-SPAN; SIRT1; LONGEVITY; RECEPTOR;
D O I
10.1016/j.bbamcr.2011.03.001
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 forkhead box O transcription factors convert a variety of external stimuli, including growth factors, nutrients, and oxidative stress, into diverse biological responses through modulation of specific gene expression. Forkhead box O regulation is principally achieved by two distinct mechanisms: post-translational modifications and protein-protein interactions. Among several modifications of forkhead box O factors, we focus on reversible acetylation, describing past research and current advances. In the latter part of this review, we also provide an overview of forkhead box O-binding partners that control the transcriptional activity of forkhead box O factors. These two layers of regulation mostly overlap and thereby enable a more precise fine-tuning of forkhead box O functions involved in metabolism, longevity, and tumor suppression. This article is part of a Special Issue entitled: PI3K-AKT-FoxO axis in cancer and aging. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1954 / 1960
页数:7
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