Molecular mechanisms underlying genotype-dependent responses to dietary restriction

被引:104
|
作者
Schleit, Jennifer [1 ]
Johnson, Simon C. [1 ]
Bennett, Christopher F. [1 ,2 ]
Simko, Marissa [1 ]
Trongtham, Natalie [1 ]
Castanza, Anthony [1 ]
Hsieh, Edward J. [3 ]
Moller, Richard M. [1 ]
Wasko, Brian M. [1 ]
Delaney, Joe R. [1 ,2 ]
Sutphin, George L. [1 ,2 ]
Carr, Daniel [1 ]
Murakami, Christopher J. [1 ]
Tocchi, Autumn [1 ]
Xian, Bo [4 ]
Chen, Weiyang [4 ]
Yu, Tao [4 ]
Goswami, Sarani [1 ]
Higgins, Sean [1 ]
Holmberg, Mollie [1 ]
Jeong, Ki-Soo [1 ]
Kim, Jin R. [1 ]
Klum, Shannon [1 ]
Liao, Eric [1 ]
Lin, Michael S. [1 ]
Lo, Winston [1 ]
Miller, Hillary [1 ]
Olsen, Brady [1 ]
Peng, Zhao J. [1 ]
Pollard, Tom [1 ]
Pradeep, Prarthana [1 ]
Pruett, Dillon [1 ]
Rai, Dilreet [1 ]
Ros, Vanessa [1 ]
Singh, Minnie [1 ]
Spector, Benjamin L. [1 ]
Vander Wende, Helen [1 ]
An, Elroy H. [1 ]
Fletcher, Marissa [1 ]
Jelic, Monika [1 ]
Rabinovitch, Peter S. [1 ]
MacCoss, Michael J. [3 ]
Han, Jing-Dong J. [4 ]
Kennedy, Brian K. [5 ,6 ]
Kaeberlein, Matt [1 ,6 ]
机构
[1] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[2] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[4] Chinese Acad Sci, Shanghai Inst Biol Sci, CAS Max Planck Partner Inst Computat Biol, CAS Key Lab Computat Biol, Shanghai, Peoples R China
[5] Buck Inst Age Res, Novato, CA USA
[6] Guangdong Med Coll, Inst Aging Res, Dongguan, Peoples R China
关键词
aging; replicative lifespan; longevity; yeast; dietary restriction; mitochondria; mitochondrial unfolded protein response; EXTENDS LIFE-SPAN; CALORIC RESTRICTION; MITOCHONDRIAL PROTEINS; PROHIBITINS; TRANSLATION; INHIBITION; LONGEVITY; EXTENSION; INCREASE; DISEASE;
D O I
10.1111/acel.12130
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dietary restriction (DR) increases lifespan and attenuates age-related phenotypes in many organisms; however, the effect of DR on longevity of individuals in genetically heterogeneous populations is not well characterized. Here, we describe a large-scale effort to define molecular mechanisms that underlie genotype-specific responses to DR. The effect of DR on lifespan was determined for 166 single gene deletion strains in Saccharomyces cerevisiae. Resulting changes in mean lifespan ranged from a reduction of 79% to an increase of 103%. Vacuolar pH homeostasis, superoxide dismutase activity, and mitochondrial proteostasis were found to be strong determinants of the response to DR. Proteomic analysis of cells deficient in prohibitins revealed induction of a mitochondrial unfolded protein response (mtUPR), which has not previously been described in yeast. Mitochondrial proteotoxic stress in prohibitin mutants was suppressed by DR via reduced cytoplasmic mRNA translation. A similar relationship between prohibitins, the mtUPR, and longevity was also observed in Caenorhabditis elegans. These observations define conserved molecular processes that underlie genotype-dependent effects of DR that may be important modulators of DR in higher organisms.
引用
收藏
页码:1050 / 1061
页数:12
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