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SPELL Version 2.0.3

Citation Honjoh S, Yamamoto T, Uno M, Nishida E. Signalling through RHEB-1 mediates intermittent fasting-induced longevity in C. elegans. Nature, 2009.
PubMed ID 19079239
Short Description Signalling through RHEB-1 mediates intermittent fasting-induced longevity in C. elegans.
GEO Record: GSE9682 Platform: GPL200
Download gene-centric, log2 transformed data: WBPaper00032430.ce.mr.csv
# of Conditions 24
Full Description 1316625150_help Dietary restriction is the most effective and reproducible intervention to extend lifespan in divergent species. In mammals, two regimens of dietary restriction, intermittent fasting (IF) and chronic caloric restriction, have proven to extend lifespan and reduce the incidence of age-related disorders. An important characteristic of IF is that it can increase lifespan even when there is little or no overall decrease in calorie intake. The molecular mechanisms underlying IF-induced longevity, however, remain largely unknown. Here we establish an IF regimen that effectively extends the lifespan of Caenorhabditis elegans, and show that the low molecular weight GTPase RHEB-1 has a dual role in lifespan regulation; RHEB-1 is required for the IF-induced longevity, whereas inhibition of RHEB-1 mimics the caloric-restriction effects. RHEB-1 exerts its effects in part by the insulin/insulin growth factor (IGF)-like signalling effector DAF-16 in IF. Our analyses demonstrate that most fasting-induced upregulated genes require RHEB-1 function for their induction, and that RHEB-1 and TOR signalling are required for the fasting-induced downregulation of an insulin-like peptide, INS-7. These findings identify the essential role of signalling by RHEB-1 in IF-induced longevity and gene expression changes, and suggest a molecular link between the IF-induced longevity and the insulin/IGF-like signalling pathway.
Experimental Details:
WBPaper00032430:N2-controlRNAi-fed_1
WBPaper00032430:N2-controlRNAi-fed_2
WBPaper00032430:N2-controlRNAi-fed_3
WBPaper00032430:N2-controlRNAi-fed_4
WBPaper00032430:N2-controlRNAi-fed_5
WBPaper00032430:N2-controlRNAi-fasting_1
WBPaper00032430:N2-controlRNAi-fasting_2
WBPaper00032430:N2-controlRNAi-fasting_3
WBPaper00032430:N2-controlRNAi-fasting_4
WBPaper00032430:N2-controlRNAi-fasting_5
WBPaper00032430:N2-Cel-RhebRNAi-fed_1
WBPaper00032430:N2-Cel-RhebRNAi-fed_2
WBPaper00032430:N2-Cel-RhebRNAi-fed_3
WBPaper00032430:N2-Cel-RhebRNAi-fed_4
WBPaper00032430:N2-Cel-RhebRNAi-fasting_1
WBPaper00032430:N2-Cel-RhebRNAi-fasting_2
WBPaper00032430:N2-Cel-RhebRNAi-fasting_3
WBPaper00032430:N2-Cel-RhebRNAi-fasting_4
WBPaper00032430:N2-Cel-TORRNAi-fed_1
WBPaper00032430:N2-Cel-TORRNAi-fed_2
WBPaper00032430:N2-Cel-TORRNAi-fed_3
WBPaper00032430:N2-Cel-TORRNAi-fasting_1
WBPaper00032430:N2-Cel-TORRNAi-fasting_2
WBPaper00032430:N2-Cel-TORRNAi-fasting_3.
Tags 1316625150_help
Method: microarray, Species: Caenorhabditis elegans, Topic: aging, Topic: response to starvation