Gene-diet interactions and aging in C. elegans

被引:25
作者
Yen, Chia An [1 ]
Curran, Sean P. [1 ,2 ]
机构
[1] Univ Southern Calif, Dornsife Coll Letters Arts & Sci, Dept Mol & Computat Biol, Los Angeles, CA 90007 USA
[2] Univ Southern Calif, Davis Sch Gerontol, Los Angeles, CA USA
关键词
Diet-gene pairs; C; elegans; Metabolism; E; coli; LIFE-SPAN EXTENSION; RESTRICTION-INDUCED LONGEVITY; SYSTEMATIC RNAI SCREEN; AGE-1; PI3; KINASE; CAENORHABDITIS-ELEGANS; CALORIC RESTRICTION; LARVAL DEVELOPMENT; NATURAL VARIATION; SIGNALING PATHWAY; NUCLEAR RECEPTORS;
D O I
10.1016/j.exger.2016.02.012
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Diet is the most variable aspect of life history, as most individuals have a large diversity of food choices, varying in the type and amount that they ingest. In the short-term, diet can affect metabolism and energy levels. However, in the long run, the net deficiency or excess of calories from diet can influence the progression and severity of age related diseases. An old and yet still debated question is: how do specific dietary choices impact health-and lifespan? It is clear that genetics can play a critical role perhaps just as important as diet choices. For example, poor diet in combination with genetic susceptibility can lead to metabolic disorders, such as obesity and type 2 diabetes. Recent work in Caenorhabditis elegans has identified the existence of diet-gene pairs, where the consequence of mutating a specific gene is only realized on specific diets. Many core metabolic pathways are conserved from worm to human. Although only a handful of these diet-gene pairs has been characterized, there are potentially hundreds, if not thousands, of such interactions, which may explain the variability in the rates of aging in humans and the incidence and severity of age-related diseases. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:106 / 112
页数:7
相关论文
共 139 条
[1]   C. elegans behavior of preference choice on bacterial food [J].
Abada, Emad Abd-elmoniem ;
Sung, Hyun ;
Dwivedi, Meenakshi ;
Park, Byung-Jae ;
Lee, Sun-Kyung ;
Ahnn, Joohong .
MOLECULES AND CELLS, 2009, 28 (03) :209-213
[2]   Chromosome-scale selective sweeps shape Caenorhabditis elegans genomic diversity [J].
Andersen, Erik C. ;
Gerke, Justin P. ;
Shapiro, Joshua A. ;
Crissman, Jonathan R. ;
Ghosh, Rajarshi ;
Bloom, Joshua S. ;
Felix, Marie-Anne ;
Kruglyak, Leonid .
NATURE GENETICS, 2012, 44 (03) :285-U83
[3]  
[Anonymous], 2012, NATURE NUTR UNIFYING
[4]   Nuclear hormone receptors and gene expression [J].
Aranda, A ;
Pascual, A .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1269-1304
[5]   C-elegans for anti-infective discovery [J].
Arvanitis, Marios ;
Glavis-Bloom, Justin ;
Mylonakis, Eleftherios .
CURRENT OPINION IN PHARMACOLOGY, 2013, 13 (05) :769-774
[6]   Obesity, Diabetes and Atrial Fibrillation; Epidemiology, Mechanisms and Interventions [J].
Asghar, O. ;
Alam, U. ;
Hayat, S. A. ;
Aghamohammadzadeh, R. ;
Heagerty, A. M. ;
Malik, R. A. .
CURRENT CARDIOLOGY REVIEWS, 2012, 8 (04) :253-264
[7]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[8]   Food transport in the C-elegans pharynx [J].
Avery, L ;
Shtonda, BB .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2003, 206 (14) :2441-2457
[9]   CONTROL OF LARVAL DEVELOPMENT BY CHEMOSENSORY NEURONS IN CAENORHABDITIS-ELEGANS [J].
BARGMANN, CI ;
HORVITZ, HR .
SCIENCE, 1991, 251 (4998) :1243-1246
[10]   ODORANT-SELECTIVE GENES AND NEURONS MEDIATE OLFACTION IN C-ELEGANS [J].
BARGMANN, CI ;
HARTWIEG, E ;
HORVITZ, HR .
CELL, 1993, 74 (03) :515-527