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WormBase Tree Display for Analysis: Microarray_Study.WBPaper00050520.ce.mr

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Name Class

Microarray_Study.WBPaper00050520.ce.mrDB_infoDatabaseGEOGSE84894
TitleExpression data from starved first larval stage of wildtype and hyl-1(ok976); lagr-1(gk327) C. elegans
DescriptionOur understanding of cellular mechanisms by which animals regulate their response to starvation is limited despite the close relevance of the problem to major human health issues. L1 diapause of Caenorhabditis elegans, where newly hatched first stage larval arrested in response to food-less environment, is an excellent system to study the problem. We found through genetic manipulation and lipid analysis that ceramide biosynthesis, particularly those with longer fatty acid side chains, critically impacts animal survival during L1 diapause. Genetic and expression analyses indicate that ceramide likely regulate this response by affecting gene expression and activity in multiple regulatory pathways known to regulate starvation-induced stress, including the insulin-IGF-1 signaling (IIS) pathway, Rb and other pathways that mediate pathogen/toxin/oxidative stress responses. These findings provide an important insight into the roles of sphingolipid metabolism in not only starvation response but also aging and food-response related human health problems.
Categoryresponse to starvation
Microarray_experimentWBPaper00050520:N2_starved-L1_rep1
WBPaper00050520:N2_starved-L1_rep2
WBPaper00050520:N2_starved-L1_rep3
WBPaper00050520:hyl-1(ok976);lagr-1(gk327)_starved-L1_rep1
WBPaper00050520:hyl-1(ok976);lagr-1(gk327)_starved-L1_rep2
WBPaper00050520:hyl-1(ok976);lagr-1(gk327)_starved-L1_rep3
Species_in_analysisCaenorhabditis elegans
ReferenceWBPaper00050520