Phosphorylation and acetylation modifications of FOXO3a: Independently or synergistically?

被引:124
作者
Wang, Xianwang [1 ]
Hu, Shujuan [2 ]
Liu, Lei [3 ,4 ]
机构
[1] Yangtze Univ, Sch Med, Lab Neuronal Network & Brain Dis Modulat, 1 South Circle Rd, Jingzhou 434023, Hubei, Peoples R China
[2] Yangtze Univ, Inst Phys Educ, Jingzhou 434023, Hubei, Peoples R China
[3] South China Normal Univ, MOE Key Lab Laser Life Sci, 55 Zhongshan Rd West, Guangzhou 510631, Guangdong, Peoples R China
[4] South China Normal Univ, Inst Laser Life Sci, Coll Biophoton, 55 Zhongshan Rd West, Guangzhou 510631, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
FOXO3a; phosphorylation; acetylation; SIRT1; transactivation; FORKHEAD TRANSCRIPTION FACTOR; OXIDATIVE STRESS; POSTTRANSLATIONAL MODIFICATIONS; PROMOTES TUMORIGENESIS; CELL-PROLIFERATION; INHIBITING FOXO3A; SIGNALING PATHWAY; SURVIVAL; CANCER; AKT;
D O I
10.3892/ol.2017.5851
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Forkhead box class O 3a (FOXO3a) is a transcription factor that has emerged as being a tumor suppressor and longevity factor. The precise regulation of FOXO3a trans activation of target genes is achieved via post-translational modifications (PTMs) and specific protein-protein interactions. The multiple types of PTMs that FOXO3a undergoes, including phosphorylation, acetylation, methylation and ubiquitination, serve important roles in directing its subcellular localization and transcription activity, which arc central to the integration of insulin/growth factor signaling and oxidative/nutrient stress signaling. The present review summarizes the modifications of FOXO3a that occur via phosphorylation and acetylation. In addition, the synergistic effect of multiple phosphorylations on FOXO3a and the crosstalk between phosphorylation and acetylation in the regulation of FOXO3a are discussed. These discussions may highlight potential strategies for the prevention of cancer and aging.
引用
收藏
页码:2867 / 2872
页数:6
相关论文
共 47 条
[1]   Posttranslational modifications control FoxO3 activity during denervation [J].
Bertaggia, Enrico ;
Coletto, Luisa ;
Sandri, Marco .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2012, 302 (03) :C587-C596
[2]   c-Jun N-terminal Kinase Enhances MST1-mediated Pro-apoptotic Signaling through Phosphorylation at Serine 82 [J].
Bi, Wenzhi ;
Xiao, Lei ;
Jia, Yunfeng ;
Wu, Junbing ;
Xie, Qi ;
Ren, Jian ;
Ji, Guangju ;
Yuan, Zengqiang .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (09) :6259-6264
[3]   Regulation of Foxo-Dependent Transcription by Post-Translational Modifications [J].
Boccitto, Marco ;
Kalb, Robert G. .
CURRENT DRUG TARGETS, 2011, 12 (09) :1303-1310
[4]   Protein kinase SGK mediates survival signals by phosphorylating the forkhead transcription factor FKHRL1 (FOXO3a) [J].
Brunet, A ;
Park, J ;
Tran, H ;
Hu, LS ;
Hemmings, BA ;
Greenberg, ME .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (03) :952-965
[5]   Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor [J].
Brunet, A ;
Bonni, A ;
Zigmond, MJ ;
Lin, MZ ;
Juo, P ;
Hu, LS ;
Anderson, MJ ;
Arden, KC ;
Blenis, J ;
Greenberg, ME .
CELL, 1999, 96 (06) :857-868
[6]   Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase [J].
Brunet, A ;
Sweeney, LB ;
Sturgill, JF ;
Chua, KF ;
Greer, PL ;
Lin, YX ;
Tran, H ;
Ross, SE ;
Mostoslavsky, R ;
Cohen, HY ;
Hu, LS ;
Cheng, HL ;
Jedrychowski, MP ;
Gygi, SP ;
Sinclair, DA ;
Alt, FW ;
Greenberg, ME .
SCIENCE, 2004, 303 (5666) :2011-2015
[7]   The FoxO code [J].
Calnan, D. R. ;
Brunet, A. .
ONCOGENE, 2008, 27 (16) :2276-2288
[8]   AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity [J].
Canto, Carles ;
Gerhart-Hines, Zachary ;
Feige, Jerome N. ;
Lagouge, Marie ;
Noriega, Lilia ;
Milne, Jill C. ;
Elliott, Peter J. ;
Puigserver, Pere ;
Auwerx, Johan .
NATURE, 2009, 458 (7241) :1056-U140
[9]   Mst1 regulates glioma cell proliferation via the AKT/mTOR signaling pathway [J].
Chao, Yuewen ;
Wang, Yan ;
Liu, Xuejiao ;
Ma, Peng ;
Shi, Yi ;
Gao, Jian ;
Shi, Qiong ;
Hu, Jinxia ;
Yu, Rutong ;
Zhou, Xiuping .
JOURNAL OF NEURO-ONCOLOGY, 2015, 121 (02) :279-288
[10]   CO-CRYSTAL STRUCTURE OF THE HNF-3/FORK HEAD DNA-RECOGNITION MOTIF RESEMBLES HISTONE-H5 [J].
CLARK, KL ;
HALAY, ED ;
LAI, ES ;
BURLEY, SK .
NATURE, 1993, 364 (6436) :412-420