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WormBase Tree Display for Expr_pattern: Expr2985

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Name Class

Expr2985Expression_ofGeneWBGene00004010
Reflects_endogenous_expression_ofWBGene00004010
Expression_dataLife_stageWBls:0000024
WBls:0000038
WBls:0000027
WBls:0000035
WBls:0000041
WBls:0000015
WBls:0000021
WBls:0000010
WBls:0000013
GO_termGO:0005737
Subcellular_localizationMost if not all PHA-1::GFP fusion protein localized to the cytoplasm. This was particularly apparent in larvae, where the contribution of nonspecific GFP fluorescence coming from layers outside of the central focal plane was minimized. No evidence was observed for any dynamic regulation of PHA-1 with respect to its subcellular localization. Although these findings do not rule out the possibility that some PHA-1 protein may normally be present in nuclei, they strongly suggest that PHA-1 resides primarily, if not exclusively, in the cytoplasmic compartment. Moreover, although it was possible that the tagged fusion protein may have been mislocalized, either due to the presence of the C-terminal GFP extension, or simply through overexpression, the ability of the fusion protein to substitute functionally for wild-type PHA-1 suggests that it is localizing to the correct cellular compartment.
TypeReporter_gene
PatternExpression of the pha-1 reporter was first detected at the approximately 100-cell stage in all somatic cells of the embryo. This pattern of widespread expression continued through later stages of embryonic development, diminishing somewhat in intensity by the time of hatching. Expression was also observed in early-larval-stage animals and was present but reduced in late-stage larvae and adults.
RemarkSimilar expression patterns were also observed using reporter constructs containing approximately 2.9 kb of upstream regulatory sequences together with genomic sequences encoding the first 137 aa of PHA-1 fused to a GFP containing a nuclear localization signal.
ReferenceWBPaper00024215
TransgeneWBTransgene00028290