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Citation Zhang Z, Liu L, Twumasi-Boateng K, Block DH, Shapira M. FOS-1 functions as a transcriptional activator downstream of the C. elegans JNK homolog KGB-1. Cell Signal, 2016.
PubMed ID 27864060
Short Description FOS-1 functions as a transcriptional activator downstream of the C. elegans JNK homolog KGB-1.
GEO Record: GSE82238 Platform: GPL9458
Download gene-centric, log2 transformed data: WBPaper00050448.ce.mr.csv
# of Conditions 33
Full Description 1316625150_help JNK proteins are conserved stress-activated MAP kinases. In C. elegans, the JNK-homolog KGB-1 plays essential roles in protection from heavy metals and protein folding stress. However, the contributions of KGB-1 are age-dependent, providing protection in larvae, but reducing stress resistance and shortening lifespan in adults. Attenuation of DAF-16 was linked to the detrimental contributions of KGB-1 in adults, but its involvement in KGB-1-dependent protection in larvae remains unclear. To characterize age-dependent contributions of KGB-1, we used microarray analysis to measure gene expression following KGB-1 activation either in developing larvae or in adults, achieved by knocking down its negative phosphatase regulator vhp-1. This revealed a robust KGB-1 regulon, most of which consisting of genes induced following KGB-1 activation regardless of age; a smaller number of genes was regulated in an age-dependent manner. We found that the bZIP transcription factor FOS-1 was essential for age-invariant KGB-1-dependent gene induction, but not for age-dependent expression. The latter was more affected by DAF-16, which was further found to be required for KGB-1-dependent cadmium resistance in larvae. Our results identify FOS-1 as a transcriptional activator mediating age-invariant contributions of KGB-1, including a regulatory loop of KGB-1 signaling, but also stress the importance of DAF-16 as a mediator of age-dependent contributions.
Experimental Details:
WBPaper00050448:N2_control(RNAi)_development_rep1
WBPaper00050448:N2_control(RNAi)_development_rep2
WBPaper00050448:N2_control(RNAi)_development_rep3
WBPaper00050448:N2_vhp-1(RNAi)_development_rep1
WBPaper00050448:N2_vhp-1(RNAi)_development_rep2
WBPaper00050448:N2_vhp-1(RNAi)_development_rep3
WBPaper00050448:N2_control(RNAi)_adult_rep1
WBPaper00050448:N2_control(RNAi)_adult_rep2
WBPaper00050448:N2_control(RNAi)_adult_rep3
WBPaper00050448:N2_vhp-1(RNAi)_adult_rep1
WBPaper00050448:N2_vhp-1(RNAi)_adult_rep2
WBPaper00050448:N2_vhp-1(RNAi)_adult_rep3
WBPaper00050448:kgb-1(km21)_control(RNAi)_development_rep1
WBPaper00050448:kgb-1(km21)_control(RNAi)_development_rep2
WBPaper00050448:kgb-1(km21)_control(RNAi)_development_rep3
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_development_rep1
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_development_rep2
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_development_rep3
WBPaper00050448:kgb-1(km21)_control(RNAi)_adult_rep1
WBPaper00050448:kgb-1(km21)_control(RNAi)_adult_rep2
WBPaper00050448:kgb-1(km21)_control(RNAi)_adult_rep3
WBPaper00050448:kgb-1(km21)_control(RNAi)_adult_rep4
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_adult_rep1
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_adult_rep2
WBPaper00050448:kgb-1(km21)_vhp-1(RNAi)_adult_rep3
WBPaper00050448:daf-16(mu86);pmk-1(km25)_control(RNAi)_development_rep1
WBPaper00050448:daf-16(mu86);pmk-1(km25)_control(RNAi)_development_rep2
WBPaper00050448:daf-16(mu86);pmk-1(km25)_vhp-1(RNAi)_development_rep1
WBPaper00050448:daf-16(mu86);pmk-1(km25)_vhp-1(RNAi)_development_rep2
WBPaper00050448:daf-16(mu86);pmk-1(km25)_control(RNAi)_adult_rep1
WBPaper00050448:daf-16(mu86);pmk-1(km25)_control(RNAi)_adult_rep2
WBPaper00050448:daf-16(mu86);pmk-1(km25)_vhp-1(RNAi)_adult_rep1
WBPaper00050448:daf-16(mu86);pmk-1(km25)_vhp-1(RNAi)_adult_rep2.
Tags 1316625150_help
Method: microarray, Species: Caenorhabditis elegans, Topic: RNAi gene function study, Topic: WT vs. mutant