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

被引:92
|
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
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