C. elegans SIR-2.1 interacts with 14-3-3 proteins to activate DAF-16 and extend life span

被引:302
作者
Berdichevsky, Ala
Viswanathan, Mohan
Horvitz, H. Robert
Guarente, Leonard
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cell.2006.04.036
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 longevity of Caenorhabditis elegans is promoted by extra copies of the sir-2.1 gene in a manner dependent on the forkhead transcription factor DAF-16. We identify two C. elegans 14-3-3 proteins as SIR-2.1 binding partners and show that 14-3-3 genes are required for the life-span extension conferred by extra copies of sir-2.1. 14-3-3 proteins are also required for SIR-2.1-induced transcriptional activation of DAF-16 and stress resistance. Following heat stress, SIR-2.1 can bind DAF-16 in a 14-3-3-dependent manner. Ely contrast, low insulin-like signaling does not promote SIR-2.1/DAF-16 interaction, and sir-2.1 and the 14-3-3 genes are not required for the regulation of life span by the insulin-like signaling pathway. We propose the existence of a stress-dependent pathway in which SIR-2.1 and 14-3-3 act in parallel to the insulin-like pathway to activate DAF16 and extend life span.
引用
收藏
页码:1165 / 1177
页数:13
相关论文
共 58 条
  • [1] The Sir2 family of protein deacetylases
    Blander, G
    Guarente, L
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 : 417 - 435
  • [2] SIRT1 deacetylation and repression of p300 involves lysine residues 1020/1024 within the cell cycle regulatory domain 1
    Bouras, T
    Fu, MF
    Sauve, AA
    Wang, F
    Quong, AA
    Perkins, ND
    Hay, RT
    Gu, W
    Pestell, RG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (11) : 10264 - 10276
  • [3] BRENNER S, 1974, GENETICS, V77, P71
  • [4] 14-3-3 transits to the nucleus and participates in dynamic nucleocytoplasmic transport
    Brunet, A
    Kanai, F
    Stehn, J
    Xu, J
    Sarbassova, D
    Frangioni, JV
    Dalal, SN
    DeCaprio, JA
    Greenberg, ME
    Yaffe, MB
    [J]. JOURNAL OF CELL BIOLOGY, 2002, 156 (05) : 817 - 828
  • [5] Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor
    Brunet, A
    Bonni, A
    Zigmond, MJ
    Lin, MZ
    Juo, P
    Hu, LS
    Anderson, MJ
    Arden, KC
    Blenis, J
    Greenberg, ME
    [J]. CELL, 1999, 96 (06) : 857 - 868
  • [6] Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase
    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
    [J]. 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
    Cahill, CM
    Tzivion, G
    Nasrin, N
    Ogg, S
    Dore, J
    Ruvkun, G
    Alexander-Bridges, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) : 13402 - 13410
  • [8] Translocation of C. elegans CED-4 to nuclear membranes during programmed cell death
    Chen, FL
    Hersh, BM
    Conradt, B
    Zhou, Z
    Riemer, D
    Gruenbaum, Y
    Horvitz, HR
    [J]. SCIENCE, 2000, 287 (5457) : 1485 - 1489
  • [9] Calorie restriction promotes mammalian cell survival by inducing the SIRT1 deacetylase
    Cohen, HY
    Miller, C
    Bitterman, KJ
    Wall, NR
    Hekking, B
    Kessler, B
    Howitz, KT
    Gorospe, M
    de Cabo, R
    Sinclair, DA
    [J]. SCIENCE, 2004, 305 (5682) : 390 - 392
  • [10] The molecular basis of FHA Domain:Phosphopeptide binding specificity and implications for phospho-dependent signaling mechanisms
    Durocher, D
    Taylor, IA
    Sarbassova, D
    Haire, LF
    Westcott, SL
    Jackson, SP
    Smerdon, SJ
    Yaffe, MB
    [J]. MOLECULAR CELL, 2000, 6 (05) : 1169 - 1182