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WormBase Tree Display for Interaction: WBInteraction000501565

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Name Class

WBInteraction000501565Interaction_typeRegulatory
InteractorInteractor_overlapping_geneWBGene00002299Interactor_typeTrans_regulator
WBGene00002992Interactor_typeTrans_regulator
WBGene00002996Interactor_typeTrans_regulator
WBGene00004400Interactor_typeTrans_regulated
Expr_patternExpr3457
Variation_interactorWBVar00143988Interactor_typeTrans_regulator
Interaction_summaryTo test whether the inductive AC signal is required for the elevated rom-1::nls::gfp expression in the proximal VPCs, the precursors of the somatic gonad Z1 and Z4 in zhIs5 animals was ablated. Uniformly low rom-1::nls::gfp expression was found in all six VPCs of gonad-ablated zhIs5 animals at the late L2 to early L3 stage, before the descendants of the tertiary VPCs had fused to hyp7. To test whether rom-1::nls::gfp expression depends on RTK/RAS-/MAPK signaling in the VPCs, the zhIs5 transgene was introduced into lin-7(e1413) mutants that exhibit a penetrant Vul phenotype due to reduced LET-23 EGFR activity. In lin-7(e1413); zhIs5 animals, the up-regulation of rom-1::nls::gfp occurred less frequently (in 13%, 33%, and 7% of the cases in P5.p, P6.p, and P7.p, respectively, n = 15). Thus, the AC signal up-regulates rom-1::nls::gfp expression in the VPCs that adopt vulval cell fates.
Detection_methodReporter_gene[rom-1::nls-gfp] translational fusion. A transcriptional rom-1 reporter was generated by fusing 6.9 kb of the 5 rom-1 promoter/enhancer region to the green fluorescent protein (gfp) ORF carrying a nuclear localizing signal (zhIs5[rom-1::nls::gfp]).
PaperWBPaper00024876