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WormBase Tree Display for RNAi: WBRNAi00088416

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Name Class

WBRNAi00088416HomolHomol_homolF10G7:RNAi
Sequence_infoDNA_textATGTTCTATGCACAGTTCGTTCTCGCCAAAAAGGGACCGTTGGCAAAAGTGTGGCTGGCAGCTCACTGGGAAAAAAAGCTGACAAAGGCGCAAATCTTCGAAACAGATGTTCCCCAAGCGATCGAGGAAGTCATTCGCCCCAAGGTTAAAATGGCGCTCCGAACAGTTGGACATCTTCTCCTTGGAATCGTGAGAATCTACTCGAAGAAGACACGATATCTTCTGGCTGATACAAATGAAGCGTATCAAAAGATGAAGATTAACTTCCGCAACGGATTCAGTTTTGAAGTCGACATTCCAGAGAATGCAGAAATTGAAGAGGATTTCTCAAACTTCATTGATAAGTACAATATCACAGTGCCCGAGTTCCACGATGCCGACTACAATGAGCAGCTCATTATGGCTAATGTGAGCCGTCGTGAAGACATCACCATGAAAGAAACCGTCAATTTCAATGTCGAGTTCAACATTGACGCAGATTTCGATGGGTTCGGTGACGAAGGAGAATCTTGGCAACTCGATCATCTCTACGGATCGGTGGAACCTTTGTCTTTGCGCCCCACTCCTCAGCCAGAATCGTTGATGGAAGTCGAACGAGATCGTGATGTGGCTGCAAATGGAACGGAAATTTCCCGTATAGATGCGGATAGTGTGATTTTCTCCGAAGGACCAACACGTCCAAATCTTATTTTTGACAATCAGGAAGGCGGAAATTTCATGCCTGAAATGAACCTGAAGGTTGAGAATCAAACACTGGAAAACGATGGTGGTGTTGGGCCTGCTGATATGTTCAGCTCAATGATTCATCCCGTCAGAGAGCATGCTGTCGCAGATGTTCAAAACGACGATGGTATGGACTTTGACTATCAACCGTTCGAGCCTGAAAACGTTGAGCCATCGAGACCACAAAGTCCCGAGTCATTTGCCCTGGAGCCTCTAGATGTGGAGCACATGGAAGGACGGAAAAAACGTCAGAGAAAAGCGAGAAAGCTGATTGTCGATGCTGAAACTATGATTTCAAACGACGCTTTCCGAGAGCAACAAGAAGACTTCTCCGATACGATGCGAGTAGTTGAAATGGCGCCTCCTACCAGAAAGATGTTCAATTTATGCGTCAGCGGAGATCTTCAACACCTCAGCCGTGAACCTGGATGCAAAATGTTCAACAGAGAACTCCTTCAAAGATACAGGAGATGTTTGGTCACCCGAGAGTTCGATCTCAATTACACCATGCAAGAGTTGAGCGATAGTTCGAGTTTCACTCCGTCAATGGAAGCTCAAGCTGAGCCATGGGAGGACTTGAACCTCAATGAGGACATTCAAGAAGATATTCAAGCGCAGGGACCAGCCGTTGATGAATTCTTTAATGATGTGCGCATGGATGATGATGATGACAGACAACCAGCTCAGGAAATGGACTTTGGTGACAACTTCGATTTTCCACAAGAAGTAGAACATCAAGAGTGTGCTCCGATCCCTATCCAGAGTGGATTCGCTGGAGAGAACAAAGAGAACGAGGACGCAGAGGATTGGTCTGATCCGTTCGGTTCTTCAAATTCCAGCAGACGTGGCCAGCTTGAAGCCTATGGATTCGGAAATACTTCGACCTACAAGGAAGACGATGGCAAATGGGCGAAACGCGCCAAGCACATTCTAAAGAAAGTCTCCGCGGATATTGAGACTTCGGGACAAGCGGACTTCTCATCTGTCACAGCAACTGCCAAGAATCGCAAGCAAGCTGCAGAGCAATTTTATTCGTTGCTTACCCTGGCCAAGTCTCAAGCAATAAGTGTTGATCAATCAGAGCCATACGGAGAGATCGTAATTCGTCCAGGAGCCAATTTCAAAGAAGCATGTCCACTGAGCTCTCCGAAACCGATGGGACTTGGAAATACAATGGAAAATTCCACTATGAGAACCCCAATGAGACCAGTTTAA
ExperimentLaboratoryYM
Date01 Jun 2003 00:00:00
StrainWBStrain00000001
Temperature20
Delivered_bySoaking
InhibitsPredicted_geneF10G7.4Inferred_automaticallyRNAi_primary
GeneWBGene00004737Inferred_automaticallyRNAi_primary
TranscriptF10G7.4.1Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00005937
PhenotypeWBPhenotype:0000050RemarkF1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes.
PenetranceComplete
WBPhenotype:0000059RemarkF1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes.
WBPhenotype:0000688RemarkF1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes.
WBPhenotype:0000697RemarkF1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes.
WBPhenotype:0000773RemarkF1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes.
PenetranceComplete
Remarkpaper remark: Exact sequence used for RNAi not stated by authors, spliced coding region sequence of gene used for curation. Authors used yk256h5(scc-1/coh-2).
MethodRNAi