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WormBase Tree Display for RNAi: WBRNAi00092769

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Name Class

WBRNAi00092769HomolHomol_homolW10C8:RNAi
Sequence_infoDNA_textATGATGGCCGACGAAGAGCTCGGCGATGAGGTGAAGGTGTTCCGTCGGGATGAGGATGCTGACGATGATCCAATGATTAGTGGTGAAACGTCAGAACAACAGTTAGCCGATGATAAAAAAGAAGCTGTAATGGAAGCAGAATTAGACGGTGCCGGTCGAAATCCATCGATTGATGTGTTAAAAAGTGCATTTCCAAAAGTCGAACCAATGTCACCATCGTTTCCCGGTTTAATGTCACACTTCAGTCCTGGATACTCGGCAGCTGCTTTACCCATGTTTATGCCTCTATTTATGAATCCATACGCAGCAGCACTACGATCACCAAGCCTGATGTTTCCAATGGGAGCAATGAGCCCCACATTTCCAATGTTCCCGCCAAGTCCTGTCTATGGAGCAGCAATCGCTGCGGCAGCCGCCAAACAACACTTTGAGAATATGGCTCCACTGAACATGCGAGCCGGTCATCCAATGAATCAGATGGGAATGCCACCATACATGCATCCATCATCAATGGCTCCACAGAATGTCGATCGAAGGGCTCAAGGAGGTGGAAAAGCGAAGAAGGATGATCATGTGAAGAAGCCATTAAACGCGTTCATGTGGTTTATGAAGGAAAATCGAAAAGCACTGCTGGAAGAGATTGGAAATAATGAGAAACAGAGTGCAGAGTTGAATAAAGAGCTTGGAAAGAGGTGGCATGATTTGTCGAAGGAAGAACAGGCGAAATATTTTGAAATGGCAAAGAAGGATAAGGAAACACACAAGGAACGGTATCCGGAGTGGTCGGCGCGGGAAAATTATGCGGTTAATAAGAAAAAGACGAAGAAACGAAGGGATAAGAGTATTCCATCGGAGAACAACGATCAGAAGAAGTGCCGAGCCAGATTCGGAGTTAACAACACAGAAATGTGGTGTAAATTCTGCAAGCGGAAGAAGAAGTGCGAGTACGCAACTGATCGTTCGGGCGGTTCCGATATAACTGACAGTCAGGATGGACGAGGTACAAGTGGTGCGTATAGCAGTAGCTCGGAGAGCCCATCACCAAAGGCAAACGCTGGAATTGCACTGACCACACAGCAGCAGCAAGCAGCAATGATGCATACGATGTTGATGCAAATGCGTCTAGGATCGACGACGGGAGCATCGACGCACGTTCCATCACCACTGGCGTCCTCGTCGGCAGGCAGGAGTCCGCTGGATGCGAACGCGTCGGATTCGGAATCTGATGTTGAGGAGGAGGAAGACGAGCAGATTGATCCGACGGTTATGCAGCAGACACATGATATGCTTATGCAGGAATCGATGTGTACTATTTAA
ExperimentLaboratoryJJ
Date01 JAN 1998 00:00:00
Genotypeglp-1(e2141); H20-GFP [neuronal marker]
Delivered_byInjection
InhibitsPredicted_geneW10C8.2Inferred_automaticallyRNAi_primary
GeneWBGene00004077Inferred_automaticallyRNAi_primary
TranscriptW10C8.2.1Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00002998
PhenotypeWBPhenotype:0000097Remarkglp-1(e2141);pop-1(RNAi) embryos had a much larger amount of hypodermal tissue than did glp-1(e2141) mutant embryos, but few if any neurons, as indicated by the lack of H20-GFP expression. The development of the first two AB daughters was analyzed individually in glp-1(e2141);pop-1(RNAi) embryos by killing all other blastomeres with a laser microbeam. Each AB daughter produced hypodermal cells almost exclusively. The lack of neurons in these experimental embryos indicates that pop-1(+) activity is required for the ABxxa fate.
WBPhenotype:0001312Remarkglp-1(e2141);pop-1(RNAi) embryos had a much larger amount of hypodermal tissue than did glp-1(e2141) mutant embryos, but few if any neurons, as indicated by the lack of H20-GFP expression. The development of the first two AB daughters was analyzed individually in glp-1(e2141);pop-1(RNAi) embryos by killing all other blastomeres with a laser microbeam. Each AB daughter produced hypodermal cells almost exclusively. The lack of neurons in these experimental embryos indicates that pop-1(+) activity is required for the ABxxa fate.
WBPhenotype:0001643Remarkglp-1(e2141);pop-1(RNAi) embryos had a much larger amount of hypodermal tissue than did glp-1(e2141) mutant embryos, but few if any neurons, as indicated by the lack of H20-GFP expression. The development of the first two AB daughters was analyzed individually in glp-1(e2141);pop-1(RNAi) embryos by killing all other blastomeres with a laser microbeam. Each AB daughter produced hypodermal cells almost exclusively. The lack of neurons in these experimental embryos indicates that pop-1(+) activity is required for the ABxxa fate.
WBPhenotype:0008001Remarkglp-1(e2141);pop-1(RNAi) embryos had a much larger amount of hypodermal tissue than did glp-1(e2141) mutant embryos, but few if any neurons, as indicated by the lack of H20-GFP expression. The development of the first two AB daughters was analyzed individually in glp-1(e2141);pop-1(RNAi) embryos by killing all other blastomeres with a laser microbeam. Each AB daughter produced hypodermal cells almost exclusively. The lack of neurons in these experimental embryos indicates that pop-1(+) activity is required for the ABxxa fate.
Remark(Figure 4, Table 2) pop-1 RNAi. Exact sequence used for RNAi not stated by authors, spliced coding region sequence of gene used for curation.
MethodRNAi