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WormBase Tree Display for RNAi: WBRNAi00102697

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Name Class

WBRNAi00102697HomolHomol_homolF08A8:RNAi
Sequence_infoPCR_productsjj_F08A8.4
ExperimentLaboratoryKQ
Date29 Apr 2008 00:00:00
Genotypemod-1(ok103)
TreatmentHT115 bacteria containing each RNAi vector were tested as described previously (Ashrafi et al., 2003) with the following modification: after overnight growth, bacteria were pelleted and resuspended to 5x concentration, 0.1 ml of which was used for seeding each well of a 12-well plate containing 4 ml NGM agar, 6 mM IPTG, and 25 mg/ml carbenicillin. Next, Nile red and 5-HT or HCl vehicle were added on top of each well, and the plates were allowed to equilibrate overnight. Twenty to thirty synchronized wild-type or mutant L1 animals were placed per well and incubated at 20 degrees Celsius to adulthood. Nile red assessment was performed on gravid adult animals. For each RNAi experiment, HT115 (vector alone) and OP50 control wells were also included. All 5-HT suppression phenotypes were confirmed by multiple (5-10) additional rounds of testing on the selected clones, whose identities were confirmed by DNA sequencing. At the time of scoring Nile red phenotypes, the identities of the target RNAi clones were unknown.
Delivered_byBacterial_feeding
InhibitsPredicted_geneF08A8.4Inferred_automaticallyRNAi_primary
GeneWBGene00008567Inferred_automaticallyRNAi_primary
TranscriptF08A8.4.1Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00031915
PhenotypeWBPhenotype:0001184RemarkF08A8.4 RNAi further suppressed the serotonin(5-HT)-induced reduction of fat content compared to mod-1(ok103) mutants alone
Affected_byMoleculeWBMol:00004929
Remark(Figure 6C, Table S3) F08A8.4 RNAi. Exact sequence used for RNAi not stated by authors, Ahringer laboratory clone used for curation.
MethodRNAi