Forward and reverse genetics approaches to uncover metabolic aging pathways in Caenorhabditis elegans

被引:17
|
作者
Gao, Arwen W. [1 ]
de Bos, Jelmi Uit [1 ]
Sterken, Mark G. [2 ]
Kammenga, Jan E. [2 ]
Smith, Reuben L. [1 ]
Houtkooper, Riekelt H. [1 ]
机构
[1] Acad Med Ctr Amsterdam, Lab Genet Metab Dis, NL-1105 AZ Amsterdam, Netherlands
[2] Wageningen Univ & Res, Lab Nematol, NL-6708 PB Wageningen, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2018年 / 1864卷 / 09期
基金
欧洲研究理事会;
关键词
C; elegans; Aging; Metabolism; Forward genetics; QTL mapping; Gene x environment interaction; ACTIVATED PROTEIN-KINASE; RESTRICTION-INDUCED LONGEVITY; LIFE-SPAN; C; ELEGANS; STRESS-RESPONSE; DIETARY RESTRICTION; QUANTITATIVE TRAITS; NATURAL VARIATION; MODEL ORGANISMS; COMPLEX;
D O I
10.1016/j.bbadis.2017.09.006
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 biological mechanisms of aging have been studied in depth and prominent findings in this field promote the development of new therapies for age-associated disorders. Various model organisms are used for research on aging; among these, the nematode Caenorhabditis elegans has been widely used and has provided valuable knowledge in determining the regulatory mechanisms driving the aging process. Many genes involved in lifespan regulation are associated with metabolic pathways and are influenced by genetic and environmental factors. In line with this, C. elegans provides a promising platform to study such gene by environment interactions, in either a reverse or forward genetics approach. In this review, we discuss longevity mechanisms related to metabolic networks that have been discovered in C. elegans. We also highlight the use of wild populations to study the complex genetic basis of natural variation for quantitative traits that mediate longevity.
引用
收藏
页码:2697 / 2706
页数:10
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