WormBase Tree Display for Expr_pattern: Expr2582
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Expr2582 | Expression_of | Gene | WBGene00003864 | |
---|---|---|---|---|
Reflects_endogenous_expression_of | WBGene00003864 | |||
Expression_data | Life_stage | WBls:0000006 | ||
WBls:0000007 | ||||
WBls:0000008 | ||||
Anatomy_term | WBbt:0004015 | Certain | ||
WBbt:0004422 | Certain | |||
WBbt:0005906 | Certain | |||
WBbt:0005994 | Certain | |||
WBbt:0006873 | Certain | |||
WBbt:0006874 | Certain | |||
WBbt:0006876 | Certain | |||
GO_term | GO:0043186 | |||
Subcellular_localization | The OMA-1::GFP fluorescence in the developing oocytes and one-cell embryos recapitulated the wild-type spatial and temporal patterns of OMA-1 antibody staining. The punctate staining appeared more pronounced and resembled the characteristic pattern of germline P granules. Starting with the onset of the first mitotic division, the intensity of OMA-1-GFP fluorescence rapidly decreased, and by the time the division was complete, only approximately 10% remained. Interestingly, that remaining 10% of the GFP signal in the two-cell embryo was predominantly found in the germline precursor, P1, associated with what appeared to be P granules. The GFP signal continued to decrease in two-cell embryos and again was asymmetric after the next division, with most of the remaining fluorescence segregated to P2, where it was also predominantly associated with granules. The OMA-1-GFP signal became too weak to detect in the embryo after the four-cell stage. | |||
Type | Reporter_gene | |||
Reference | WBPaper00005930 | |||
Transgene | WBTransgene00004720 |