WormBase Tree Display for RNAi: WBRNAi00101916
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WBRNAi00101916 | Homol | Homol_homol | CC4:RNAi | ||
---|---|---|---|---|---|
Sequence_info | PCR_product | sjj_CC4.2 | |||
Experiment | Laboratory | IZ | |||
Date | 18 Jul 2014 00:00:00 | ||||
Genotype | L-AChR(gf) (ufIs6) | ||||
Temperature | 20 | ||||
Delivered_by | Bacterial_feeding | ||||
Inhibits | Predicted_gene | CC4.2 | Inferred_automatically | RNAi_primary | |
Gene | WBGene00003753 | Inferred_automatically | RNAi_primary | ||
Transcript | CC4.2.1 | Inferred_automatically | RNAi_primary | ||
Species | Caenorhabditis elegans | ||||
Interaction | WBInteraction000523936 | ||||
Reference | WBPaper00045671 | ||||
Phenotype | WBPhenotype:0000643 | Remark | This RNAi was able to suppress the locomotion phenotypes found in L-AChR(gf) animals. L-AChR(gf) enhances synaptic activation of muscles by increasing L-AChR function. | ||
Remark | The authors wanted to enhance synaptic activation of muscles by increasing L-AChR function, thus they introduced an amino acid change at a highly conserved position in the pore-lining M2 regions of cDNAs encoding the UNC-29, UNC-38 and LEV-1 subunits. They constructed a strain (ufIs6) stably expressing the unc-29(L/S), unc-38(V/S) and lev-1(L/S) cDNAs under control of the muscle-specific myo-3 promoter, and refer to this as L-AChR(gf). | ||||
Method | RNAi |