14-3-3 regulates life span by both DAF-16-dependent and -independent mechanisms in Caenorhabditis elegans

被引:14
作者
Araiz, Caroline [1 ]
Chateau, Marie-Therese [1 ,2 ]
Galas, Simon [1 ,2 ]
机构
[1] CRBM CNRS, F-34293 Montpellier 5, France
[2] Univ Montpellier I, Fac Pharm, F-34093 Montpellier 5, France
关键词
C; elegans; ageing; Insulin/IGF-1/DAF-2; FOXO/DAF-16; 14-3-3/ftt1/ftt2;
D O I
10.1016/j.exger.2008.03.001
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Caenorhabditis elegans life span, stress resistance and metabolism are regulated by the Insulin/IGF-1/DAF2/DAF-16 pathway. DAF-16, a member of FOXO/Forkhead transcription factor family, can be targeted by 14-3-3 proteins to promote stress resistance. We have identified a 14-3-3 C. elegans homolog which promotes life span by both DAF-2-dependent and -independent mechanisms and by an unexpected DAF-16-independent mechanism. Our results demonstrate that C. elegans 14-3-3 proteins modulate stress-responsive genes throughout adulthood. In conclusion, 14-3-3 can be considered as an acute stressresponsive regulator as well as a sustained modulator of the Insulin/IGF-1/DAF-2/DAF-76 regulatory pathway in promoting life expectancy of growing old worms. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:505 / 519
页数:15
相关论文
共 48 条
[1]
The metabolic response of heterotrophic Arabidopsis cells to oxidative stress [J].
Baxter, Charles J. ;
Redestig, Henning ;
Schauer, Nicolas ;
Repsilber, Dirk ;
Patil, Kiran R. ;
Nielsen, Jens ;
Selbig, Joachim ;
Liu, Junli ;
Fernie, Alisdair R. ;
Sweetlove, Lee J. .
PLANT PHYSIOLOGY, 2007, 143 (01) :312-325
[2]
A stress response pathway involving sirtuins, forkheads and 14-3-3 proteins [J].
Berdichevsky, Ala ;
Guarente, Leonard .
CELL CYCLE, 2006, 5 (22) :2588-2591
[3]
C. elegans SIR-2.1 interacts with 14-3-3 proteins to activate DAF-16 and extend life span [J].
Berdichevsky, Ala ;
Viswanathan, Mohan ;
Horvitz, H. Robert ;
Guarente, Leonard .
CELL, 2006, 125 (06) :1165-1177
[4]
BRENNER S, 1974, GENETICS, V77, P71
[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]
Phosphatidylinositol 3-kinase signaling inhibits DAF-16 DNA binding and function via 14-3-3-dependent and 14-3-3-independent pathways [J].
Cahill, CM ;
Tzivion, G ;
Nasrin, N ;
Ogg, S ;
Dore, J ;
Ruvkun, G ;
Alexander-Bridges, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :13402-13410
[7]
Craparo A, 1997, J BIOL CHEM, V272, P11663
[8]
Rates of behavior and aging specified by mitochondrial function during development [J].
Dillin, A ;
Hsu, AL ;
Arantes-Oliveira, NA ;
Lehrer-Graiwer, J ;
Hsin, H ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Kenyon, C .
SCIENCE, 2002, 298 (5602) :2398-2401
[9]
Timing requirements for insulin/IGF-1 signaling in C-elegans [J].
Dillin, A ;
Crawford, DK ;
Kenyon, C .
SCIENCE, 2002, 298 (5594) :830-834
[10]
Quantitative mass spectrometry identifies insulin signaling targets in C-elegans [J].
Dong, Meng-Qiu ;
Venable, John D. ;
Au, Nora ;
Xu, Tao ;
Park, Sung Kyu ;
Cociorva, Daniel ;
Johnson, Jeffrey R. ;
Dillin, Andrew ;
Yates, John R., III .
SCIENCE, 2007, 317 (5838) :660-663