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WormBase Tree Display for Interaction: WBInteraction000542323

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Name Class

WBInteraction000542323Interaction_typeRegulatoryChange_of_localization
InteractorInteractor_overlapping_geneWBGene00002275Interactor_typeTrans_regulated
TransgeneWBTransgene00001856
ConstructWBCnstr00001838
WBGene00003210Interactor_typeTrans_regulator
Interaction_summaryAfter control RNAi treatment, GFP-LEM-2 was evenly distributed in pronuclear NEs, redistributed to the endoplasmic reticulum (ER) during mitosis, and recruited around chromosomes 60 to 100 s after anaphase entry. In mel-28(RNAi) one-cell embryos, no clear nuclear rim staining was visible despite the acquisition of several confocal sections at each time point. Small and misshapen pronuclei were sometime seen, and GFP signal concentrated around the centrosomes prior to mitosis. Later during mitosis, more GFP-LEM-2 accumulated at centrosomes than in control RNAi-treated embryos, but mitosis proceeded normally in terms of centrosome and cytokinesis. At mitotic exit, GFP-LEM-2 signal on the chromatin surface increased to a lesser degree than in the control RNAi embryos and at best formed a discontinuous, small, and misshapen NE-like structure.
Detection_methodConstruct
Reporter_gene[lem-2::gfp], translational fusion of GFP with LEM-1, driven by pie-1 promoter
Transgene
Regulation_resultNegative_regulateSubcellular_localizationaccumulated around centrosomes in mel-28(RNAi) embryos
Interaction_RNAiWBRNAi00065562
PaperWBPaper00028456