SPELL - Nematode - Dataset Details
New Search

Dataset Listing

Show Expression Levels

Download Expression Data

About the Website

SPELL Version 2.0.3

Citation Depuydt G, Xie F, Petyuk VA, Shanmugam N, Smolders A, Dhondt I, Brewer HM, Camp DG, Smith RD, Braeckman BP. Reduced insulin/insulin-like growth factor-1 signaling and dietary restriction inhibit translation but preserve muscle mass in Caenorhabditis elegans. Mol Cell Proteomics, 2013.
PubMed ID 24002365
Short Description Reduced insulin/insulin-like growth factor-1 signaling and dietary restriction inhibit translation but preserve muscle mass in Caenorhabditis elegans.
GEO Record: N.A. Platform: N.A.
Download gene-centric, log2 transformed data: WBPaper00044128.ce.ms.csv
# of Conditions 15
Full Description 1316625150_help Reduced signaling through the C. elegans insulin/insulin-like growth factor-1-like tyrosine kinase receptor daf-2 and dietary restriction via bacterial dilution are two well-characterized lifespan-extending interventions that operate in parallel or through (partially) independent mechanisms. Using accurate mass and time tag LC-MS/MS quantitative proteomics, we detected that the abundance of a large number of ribosomal subunits is decreased in response to dietary restriction, as well as in the daf-2(e1370) insulin/insulin-like growth factor-1-receptor mutant. In addition, general protein synthesis levels in these long-lived worms are repressed. Surprisingly, ribosomal transcript levels were not correlated to actual protein abundance, suggesting that post-transcriptional regulation determines ribosome content. Proteomics also revealed the increased presence of many structural muscle cell components in long-lived worms, which appeared to result from the prioritized preservation of muscle cell volume in nutrient-poor conditions or low insulin-like signaling. Activation of DAF-16, but not diet restriction, stimulates mRNA expression of muscle-related genes to prevent muscle atrophy. Important daf-2-specific proteome changes include overexpression of aerobic metabolism enzymes and general activation of stress-responsive and immune defense systems, whereas the increased abundance of many protein subunits of the proteasome core complex is a dietary-restriction-specific characteristic.
Experimental Details:
MassSpec_WBPaper00044128:control-FullyFed_rep1
MassSpec_WBPaper00044128:control-FullyFed_rep2
MassSpec_WBPaper00044128:control-FullyFed_rep3
MassSpec_WBPaper00044128:control-FullyFed_rep4
MassSpec_WBPaper00044128:control-FullyFed_rep5
MassSpec_WBPaper00044128:control-DietaryRestricted_rep1
MassSpec_WBPaper00044128:control-DietaryRestricted_rep2
MassSpec_WBPaper00044128:control-DietaryRestricted_rep3
MassSpec_WBPaper00044128:control-DietaryRestricted_rep4
MassSpec_WBPaper00044128:control-DietaryRestricted_rep5
MassSpec_WBPaper00044128:daf2-FullyFed_rep1
MassSpec_WBPaper00044128:daf2-FullyFed_rep2
MassSpec_WBPaper00044128:daf2-FullyFed_rep3
MassSpec_WBPaper00044128:daf2-FullyFed_rep4
MassSpec_WBPaper00044128:daf2-FullyFed_rep5.
Tags 1316625150_help
Method: proteomics, Species: Caenorhabditis elegans, Topic: response to starvation