C. elegans 14-3-3 proteins regulate life span and interact with SIR-2.1 and DAF-16/FOXO

被引:93
作者
Wang, Yamei
Oh, Seung Wook
Deplancke, Bart
Luo, Jianyuan
Walhout, Albertha J. M.
Tissenbaum, Heidi A. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA
关键词
14-3-3; SIR2; SIR-2.1; DAF-16; FOXO; Insulin/IGF-1; signaling; PAR-5; FTT-2; aging; life span; C elegans;
D O I
10.1016/j.mad.2006.05.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
14-3-3 proteins are evolutionarily conserved and ubiquitous proteins that function in a wide variety of biological processes. Here we define a new role for C elegans 14-3-3 proteins in life span regulation. We identify two C elegans 14-3-3 proteins as interacting proteins of a major life span regulator, the C. elegans SIR2 ortholog, SIR-2.1. Similar to sir-2.1, we find that overexpression of either 14-3-3 protein (PAR-5 or FTT-2) extends life span and that this is dependent on DAF-16, a forkhead transcription factor (FOXO), another important life span regulator in the insulin/IGF-1 signaling pathway. Furthermore, we show that both 14-3-3 proteins are co-expressed with DAF-16 and SIR-2.1 in the tissues critical for life span regulation. Finally, we show that DAF-16/FOXO also physically interacts with the 14-3-3 proteins. These results suggest that C. elegans 14-3-3 proteins can regulate longevity by cooperating with both SIR-2.1 and DAF-16/FOXO. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:741 / 747
页数:7
相关论文
共 41 条
[1]   Insulin/IGF-I-signaling pathway:: an evolutionarily conserved mechanism of longevity from yeast to humans [J].
Barbieri, M ;
Bonafè, M ;
Franceschi, C ;
Paolisso, G .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (05) :E1064-E1071
[2]   The Sir2 family of protein deacetylases [J].
Blander, G ;
Guarente, L .
ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 :417-435
[3]  
BRENNER S, 1974, GENETICS, V77, P71
[4]   Transcription-dependent and -independent control of neuronal survival by the PI3K-Akt signaling pathway [J].
Brunet, A ;
Datta, SR ;
Greenberg, ME .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) :297-305
[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]   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
[8]   Silent information regulator 2 potentiates Foxo1-mediated transcription through its deacetylase activity [J].
Daitoku, H ;
Hatta, M ;
Matsuzaki, H ;
Aratani, S ;
Ohshima, T ;
Miyagishi, M ;
Nakajima, T ;
Fukamizu, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (27) :10042-10047
[9]   14-3-3 proteins: Structure, function, and regulation [J].
Fu, HA ;
Subramanian, RR ;
Masters, SC .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2000, 40 :617-647
[10]   A SIMPLE METHOD FOR MAINTAINING LARGE, AGING POPULATIONS OF CAENORHABDITIS-ELEGANS [J].
GANDHI, S ;
SANTELLI, J ;
MITCHELL, DH ;
STILES, JW ;
RAOSANADI, D .
MECHANISMS OF AGEING AND DEVELOPMENT, 1980, 12 (02) :137-150