WormBase Tree Display for Expr_pattern: Expr3686
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Expr3686 | Expression_of | Gene | WBGene00001345 | |
---|---|---|---|---|
Reflects_endogenous_expression_of | WBGene00001345 | |||
Expression_data | Anatomy_term | WBbt:0004522 | Certain | |
WBbt:0005175 | Partial | |||
WBbt:0007831 | Certain | |||
WBbt:0008435 | Certain | |||
GO_term | GO:0005634 | |||
Subcellular_localization | fos-1a::YFP-TL protein localized to the nucleus | |||
Type | Reporter_gene | |||
Pattern | Transgenic animals containing the fos-1a::YFP-TX and -TL reporters showed the same expression pattern at all times examined, and fos-1a::YFP-TL protein localized to the nucleus. fos-1a::YFP-TL also rescued the AC-invasion defect when expressed in fos-1(ar105) mutants. fos-1a was expressed at the highest level in the AC and at lower levels in neighboring somatic gonad cells during AC invasion. No expression of fos-1a was detected in vulval cells. In contrast, both the fos-1b::CFP-TX and -TL reporters directed expression in vulval cells and the AC. fos-1b::CFP-TL also drove expression in neighboring uterine cells, whereas fos-1b::CFP-TX did not, suggesting the presence of a downstream uterine enhancer element in fos-1b::CFP-TL. Unlike fos-1a expression, levels of fos-1b::CFP-TL protein were not greater in the AC compared to neighboring cells. Moreover, whereas the fos-1a reporters drove expression almost exclusively in the somatic gonad cells, the fos-1b reporters directed expression in nearly all cells at the L3 stage. | |||
Picture | WBPicture0000009387 | |||
Reference | WBPaper00026611 | |||
Transgene | WBTransgene00028815 |