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WormBase Tree Display for RNAi: WBRNAi00088831

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Name Class

WBRNAi00088831HomolHomol_homolK04D7:RNAi
Sequence_infoPCR_productsjj_K04D7.1
ExperimentLaboratoryMAD
Date14 Mar 2011 00:00:00
Genotype[DYN-1::GFP]
TreatmentL4-stage hermaphrodites were fed bacteria expressing double-stranded RNA. rack-1(RNAi) experiments were performed for 40-48 hours at 20 degrees C, or 30-36 hours at 25 degrees C.
Delivered_byBacterial_feeding
InhibitsPredicted_geneK04D7.1Inferred_automaticallyRNAi_primary
GeneWBGene00010556Inferred_automaticallyRNAi_primary
TranscriptK04D7.1.1Inferred_automaticallyRNAi_primary
K04D7.1.3Inferred_automaticallyRNAi_primary
K04D7.1.2Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00038375
PhenotypeWBPhenotype:0000679RemarkIn rack-1(RNAi) embryos, the initial anterior enrichment of DYN-1-GFP foci during establishment phase was not affected (Fig. 3E; also see Video S6). However, during maintenance phase bright DYN-1-GFP puncta expanded into the posterior cortex (Fig. 3F, 7/12 embryos), and sometimes shrunk to a smaller size than that of wild type (2/12 embryos). The expansion/shrinkage was corrected with furrow initiation, and the cleavage furrow was properly placed (Fig. 3G). DYN-1 localization in the two daughter cells was normal, with the exception that in embryos with failed cytokinesis DYN-1-GFP expanded to the posterior cortex after furrow regression (Fig. 3H). We also noticed that in rack-1(RNAi) embryos, the DYN-1-GFP foci were clumping into larger foci than in wild type.
Remarkrack-1 RNAi
MethodRNAi