Transcriptional response to dietary restriction in Drosophila melanogaster

被引:14
|
作者
Ding, Feifei [1 ]
Gil, M. Pilar [1 ]
Franklin, Michael [1 ]
Ferreira, Jonathan [1 ]
Tatar, Marc [2 ]
Helfand, Stephen L. [1 ]
Neretti, Nicola [1 ,3 ]
机构
[1] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
[2] Brown Univ, Dept Ecol & Evolutionary Biol, Providence, RI 02912 USA
[3] Brown Univ, Ctr Computat Mol Biol, Providence, RI 02912 USA
关键词
Life span; Dietary restriction; Dietary switch; Gene expression; Pathway analysis; Drosophila melanogaster; LIFE-SPAN EXTENSION; CALORIC RESTRICTION; GENES; TOR; PHOSPHORYLATION; MORTALITY; HEALTH;
D O I
10.1016/j.jinsphys.2014.05.002
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Dietary restriction (DR) extends lifespan in a wide variety of organisms. Although several genes and pathways associated with this longevity response have been identified, the specific mechanism through which DR extends lifespan is not fully understood. We have recently developed a novel methodology to screen for transcriptional changes in response to acutely imposed DR upon adult Drosophila melanogaster and identified groups of genes that switch their transcriptional patterns from a normal diet pattern to a restricted diet pattern, or 'switching genes'. In this current report we extend our transcriptional data analysis with gene set enrichment analysis to generate a pathway-centered perspective. The pattern of temporal behavior in response to the diet switch is strikingly similar within and across pathways associated with mRNA processing and protein translation. Furthermore, most genes within these pathways display an initial spike in activity within 6-8 h from the diet switch, followed by a coordinated, partial down-regulation after 24 h. We propose this represents a stereotypical response to DR, which ultimately leads to a mild but widespread inhibition of transcriptional and translational activity. Inhibition of the protein synthesis pathway has been observed in DR in other studies and has been shown to extend lifespan in several model organisms. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:101 / 106
页数:6
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