Ammonium is a key determinant on the dietary restriction of yeast chronological aging in culture medium

被引:16
作者
Santos, Julia [1 ,2 ]
Leitao-Correia, Fernanda [3 ]
Sousa, Matria Joao [3 ]
Leao, Cecilia [1 ,2 ]
机构
[1] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[3] Univ Minho, Dept Biol, Mol & Environm Biol Ctr CBMA, Braga, Portugal
关键词
Ammonium; lifespan; dietary restriction; amino acid restriction; yeast; DNA-REPLICATION STRESS; LIFE-SPAN; SACCHAROMYCES-CEREVISIAE; PROTEIN-KINASE; CONTROLS TORC1; LONGEVITY; EXTENDS; HOMEOSTASIS; SUPEROXIDE; AUTOPHAGY;
D O I
10.18632/oncotarget.2989
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New evidences have recently emerged from studies in yeast and in higher eukaryotes showing the importance of nutrient balance in dietary regimes and its effects on longevity regulation. We have previously shown that manipulation of ammonium concentration in the culture and/or aging medium can drastically affect chronological lifespan (CLS) of Saccharomyces cerevisiae, especially in amino acid restricted cells. Here we describe that the CLS shortening under amino acid restriction can be completely reverted by removing ammonium from the culture medium. Furthermore, the absence of ammonium, and of any rich nitrogen source, was so effective in extending CLS that no beneficial effect could be observed by further imposing calorie restriction conditions. When present in the culture medium, ammonium impaired the consumption of the auxotrophy-complementing amino acids and caused in an improper cell cycle arrest of the culture. TOR1 deletion reverted ammonium effects both in amino acid restricted and non-restricted cultures, whereas, Ras2p and Sch9p seem to have only a milder effect in the mediation of ammonium toxicity under amino acid restriction and no effect on non-restricted cultures. Our studies highlight ammonium as a key effector in the nutritional equilibrium between rich and essential nitrogen sources and glucose required for longevity promotion.
引用
收藏
页码:6511 / 6523
页数:13
相关论文
共 51 条
[1]   Autophagy and amino acid homeostasis are required for chronological longevity in Saccharomyces cerevisiae [J].
Alvers, Ashley L. ;
Fishwick, Laura K. ;
Wood, Michael S. ;
Hu, Doreen ;
Chung, Hye S. ;
Dunn, William A., Jr. ;
Aris, John P. .
AGING CELL, 2009, 8 (04) :353-369
[2]   The Vam6 GEF Controls TORC1 by Activating the EGO Complex [J].
Binda, Matteo ;
Peli-Gulli, Marie-Pierre ;
Bonfils, Gregory ;
Panchaud, Nicolas ;
Urban, Joerg ;
Sturgill, Thomas W. ;
Loewith, Robbie ;
De Virgilio, Claudio .
MOLECULAR CELL, 2009, 35 (05) :563-573
[3]   Influence of genotype and nutrition on survival and metabolism of starving yeast [J].
Boer, Viktor M. ;
Amini, Sasan ;
Botstein, David .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (19) :6930-6935
[4]   Leucyl-tRNA Synthetase Controls TORC1 via the EGO Complex [J].
Bonfils, Gregory ;
Jaquenoud, Malika ;
Bontron, Severine ;
Ostrowicz, Clemens ;
Ungermann, Christian ;
De Virgilio, Claudio .
MOLECULAR CELL, 2012, 46 (01) :105-110
[5]   Coordination of growth rate, cell cycle, stress response, and metabolic activity in yeast [J].
Brauer, Matthew J. ;
Huttenhower, Curtis ;
Airoldi, Edoardo M. ;
Rosenstein, Rachel ;
Matese, John C. ;
Gresham, David ;
Boer, Viktor M. ;
Troyanskaya, Olga G. ;
Botstein, David .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (01) :352-367
[6]   A molecular mechanism of chronological aging in yeast [J].
Burtner, Christopher R. ;
Murakami, Christopher J. ;
Kennedy, Brian K. ;
Kaeberlein, Matt .
CELL CYCLE, 2009, 8 (08) :1256-1270
[7]   The general amino acid control pathway regulates mTOR and autophagy during serum/glutamine starvation [J].
Chen, Rui ;
Mao, Dongxue ;
Sun, Daxiao ;
Gao, Guanguang ;
Shi, Jingwen ;
Liu, Xiaoqing ;
Zhu, Chen ;
Yang, Mingyu ;
Ye, Wanlu ;
Hao, Qianqian ;
Li, Ruiqiang ;
Yu, Li .
JOURNAL OF CELL BIOLOGY, 2014, 206 (02) :173-182
[8]   The Sch9 protein kinase in the yeast Saccharomyces cerevisiae controls cAPK activity and is required for nitrogen activation of the fermentable-growth-medium-induced (FGM) pathway [J].
Crauwels, M ;
Donaton, MCV ;
Pernambuco, MB ;
Winderickx, J ;
deWinde, JH ;
Thevelein, JM .
MICROBIOLOGY-UK, 1997, 143 :2627-2637
[9]   Sequential Use of Nitrogen Compounds by Saccharomyces cerevisiae during Wine Fermentation: a Model Based on Kinetic and Regulation Characteristics of Nitrogen Permeases [J].
Crepin, Lucie ;
Nidelet, Thibault ;
Sanchez, Isabelle ;
Dequin, Sylvie ;
Camarasa, Carole .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2012, 78 (22) :8102-8111
[10]   GENETIC AND BIOCHEMICAL-EVIDENCE FOR YEAST GCN2 PROTEIN-KINASE POLYMERIZATION [J].
DIALLINAS, G ;
THIREOS, G .
GENE, 1994, 143 (01) :21-27