High osmolarity extends life span in Saccharomyces cerevisiae by a mechanism related to calorie restriction

被引:111
作者
Kaeberlein, M [1 ]
Andalis, AA
Fink, GR
Guarente, L
机构
[1] Longen Inc, Waltham, MA 02451 USA
[2] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1128/MCB.22.22.8056-8066.2002
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
Calorie restriction (CR) extends life span in many different organisms, including mammals. We describe here a novel pathway that extends the life span of Saccharomyces cerevisiae mother cells but does not involve a reduction in caloric content of the media, i.e., there is growth of yeast cells in the presence of a high concentration of external osmolytes. Like CR, this longevity-promoting response to high osmolarity requires SIR2, suggesting a common mechanism of life span regulation. Genetic and microarray analysis indicates that high osmolarity extends the life span by activating Hog1p, leading to an increase in the biosynthesis of glycerol from glycolytic intermediates. This metabolic shift likely increases NAD levels, thereby activating Sir2p and promoting longevity.
引用
收藏
页码:8056 / 8066
页数:11
相关论文
共 44 条
  • [1] GPD1, WHICH ENCODES GLYCEROL-3-PHOSPHATE DEHYDROGENASE, IS ESSENTIAL FOR GROWTH UNDER OSMOTIC-STRESS IN SACCHAROMYCES-CEREVISIAE, AND ITS EXPRESSION IS REGULATED BY THE HIGH-OSMOLARITY GLYCEROL RESPONSE PATHWAY
    ALBERTYN, J
    HOHMANN, S
    THEVELEIN, JM
    PRIOR, BA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) : 4135 - 4144
  • [2] Stress-induced MAP kinase Hog1 is part of transcription activation complexes
    Alepuz, PM
    Jovanovic, A
    Reiser, V
    Ammerer, G
    [J]. MOLECULAR CELL, 2001, 7 (04) : 767 - 777
  • [3] Manipulation of a nuclear NAD+ salvage pathway delays aging without altering steady-state NAD+ levels
    Anderson, RM
    Bitterman, KJ
    Wood, JG
    Medvedik, O
    Cohen, H
    Lin, SS
    Manchester, JK
    Gordon, JI
    Sinclair, DA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) : 18881 - 18890
  • [4] [Anonymous], 1991, Methods Enzymol, V194, P1
  • [5] Mutations in Saccharomyces cerevisiae gene SIR2 can have differential effects on in vivo silencing phenotypes and in vitro histone deacetylation activity
    Armstrong, CM
    Kaeberlein, M
    Imai, SI
    Guarente, L
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (04) : 1427 - 1438
  • [6] Isolation of hyperactive mutants of the MAPK p38/Hog1 that are independent of MAPK kinase activation
    Bell, M
    Capone, R
    Pashtan, I
    Levitzki, A
    Engelberg, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) : 25351 - 25358
  • [7] Blomberg A, 2000, FEMS MICROBIOL LETT, V182, P1
  • [8] Transcriptional silencing of Ty1 elements in the RDN1 locus of yeast
    Bryk, M
    Banerjee, M
    Murphy, M
    Knudsen, KE
    Garfinkel, DJ
    Curcio, MJ
    [J]. GENES & DEVELOPMENT, 1997, 11 (02) : 255 - 269
  • [9] Remodeling of yeast genome expression in response to environmental changes
    Causton, HC
    Ren, B
    Koh, SS
    Harbison, CT
    Kanin, E
    Jennings, EG
    Lee, TI
    True, HL
    Lander, ES
    Young, RA
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (02) : 323 - 337
  • [10] YPD™, PombePD™ and WormPD™:: model organism volumes of the BioKnowledge™ Library, an integrated resource for protein information
    Costanzo, MC
    Crawford, ME
    Hirschman, JE
    Kranz, JE
    Olsen, P
    Robertson, LS
    Skrzypek, MS
    Braun, BR
    Hopkins, KL
    Kondu, P
    Lengieza, C
    Lew-Smith, JE
    Tillberg, M
    Garrels, JI
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (01) : 75 - 79