Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

GenDR

General information

URL: http://genomics.senescence.info/diet
Full name: The Dietary restriction gene database
Description: GenDR includes two datasets: 1) genes inferred from experiments in model organisms in which genetic manipulations cancel out or disrupt the life-extending effects of DR; 2) genes robustly altered due to DR, derived from a meta-analysis of microarray DR studies in mammals.
Year founded: 2012
Last update:
Version:
Accessibility:
Accessible
Country/Region: United Kingdom

Classification & Tag

Data type:
DNA
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: University of Liverpool
Address: Institute of Ageing and Chronic Disease William Duncan Building, Room 281 University of Liverpool 6 West Derby Street, Liverpool L7 8TX United Kingdom
City: Liverpool
Province/State:
Country/Region: United Kingdom
Contact name (PI/Team): João Pedro de Magalhães
Contact email (PI/Helpdesk): jp@senescence.info

Publications

22912585
Dissecting the gene network of dietary restriction to identify evolutionarily conserved pathways and new functional genes. [PMID: 22912585]
Wuttke D, Connor R, Vora C, Craig T, Li Y, Wood S, Vasieva O, Shmookler Reis R, Tang F, de Magalhães JP.

Dietary restriction (DR), limiting nutrient intake from diet without causing malnutrition, delays the aging process and extends lifespan in multiple organisms. The conserved life-extending effect of DR suggests the involvement of fundamental mechanisms, although these remain a subject of debate. To help decipher the life-extending mechanisms of DR, we first compiled a list of genes that if genetically altered disrupt or prevent the life-extending effects of DR. We called these DR-essential genes and identified more than 100 in model organisms such as yeast, worms, flies, and mice. In order for other researchers to benefit from this first curated list of genes essential for DR, we established an online database called GenDR (http://genomics.senescence.info/diet/). To dissect the interactions of DR-essential genes and discover the underlying lifespan-extending mechanisms, we then used a variety of network and systems biology approaches to analyze the gene network of DR. We show that DR-essential genes are more conserved at the molecular level and have more molecular interactions than expected by chance. Furthermore, we employed a guilt-by-association method to predict novel DR-essential genes. In budding yeast, we predicted nine genes related to vacuolar functions; we show experimentally that mutations deleting eight of those genes prevent the life-extending effects of DR. Three of these mutants (OPT2, FRE6, and RCR2) had extended lifespan under ad libitum, indicating that the lack of further longevity under DR is not caused by a general compromise of fitness. These results demonstrate how network analyses of DR using GenDR can be used to make phenotypically relevant predictions. Moreover, gene-regulatory circuits reveal that the DR-induced transcriptional signature in yeast involves nutrient-sensing, stress responses and meiotic transcription factors. Finally, comparing the influence of gene expression changes during DR on the interactomes of multiple organisms led us to suggest that DR commonly suppresses translation, while stimulating an ancient reproduction-related process.

PLoS Genet. 2012:8(8) | 44 Citations (from Europe PMC, 2025-12-20)

Ranking

All databases:
3126/6895 (54.677%)
Health and medicine:
780/1738 (55.178%)
Interaction:
585/1194 (51.089%)
3126
Total Rank
43
Citations
3.308
z-index

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Record metadata

Created on: 2018-01-28
Curated by:
Pei Wang [2018-03-21]
Pei Wang [2018-02-23]
Hao Zhang [2018-01-28]