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WormBase Tree Display for Expr_pattern: Expr3238

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Name Class

Expr3238Expression_ofGeneWBGene00004377
Reflects_endogenous_expression_ofWBGene00004377
Expression_dataAnatomy_termWBbt:0003681Certain
WBbt:0005733Certain
WBbt:0005751Certain
WBbt:0005772Certain
WBbt:0006797Certain
GO_termGO:0005886
GO:0030132
Subcellular_localizationIn intestinal and pharyngeal cells, GFP-RME-6 was clearly concentrated on the plasma membrane. In coelomocytes, GFP-RME-6 was also localized on or very close to the plasma membrane.
Most GFP-RME-6 did not overlap with mRFP1-EEA-1 or mRFP1-RAB-5. In contrast, strong colocalization of GFP-RME-6 was found with mRFP1-CHC-1 and mRFP1-alpha-adaptin on or near the plasma membrane of coelomocytes. mRFP1-CHC-1 and mRFP1-alpha-adaptin as well as GFP-RME-6 were distributed unevenly around the plasma membrane, with regions of high and low labelling, reminiscent of the uneven distribution of endocytic pit structures that can be seen in coleomocytes by electron microscopy. Similar colocalization was observed with mRFP-RME-6 and GFP-CHC-1. These results indicate that most RME-6 is associated with clathrin-coated pits and that only a minor fraction of the RME-6 in the cells is associated with early endosomes.
Similar subcellular localization of GFP-RME-6 was observed in oocytes and the hypodermis. To analyse RME-6 distribution in oocytes, strains that express GFP-RME-6 in the rme-6(b1014) background under pie-1 promoter control were established . Expression of GFP-RME-6 in oocytes completely rescued the yolk endocytosis defect of the rme-6(b1014)-null mutant. GFP-RME-6 was concentrated on small puncta, which were on or close to the plasma membrane of oocytes. Strong colocalization of this GFP-RME-6 with mRFP1CHC-1 surface puncta was observed, indicating that RME-6 labels coated pits or vesicles. On the other hand, GFP-RME-6 in oocytes showed little spatial overlap with endogenous EEA-1, as assayed using a previously published anti-EEA-1 antibody. Clear colocalization of GFP-RME-6 and mRFP-CHC-1 was also evident in hypodermal cells. RME-6 and coated pit marker colocalization was not perfect and that the ratio of intensities of GFP-RME-6 and mRFP1-CHC-1 varied from puncta to puncta, implying that GFP-RME-6 may associate with clathrin-coated pits at a specific stage in their formation.
TypeReporter_geneTransgenic worms that expressed RME-6 with either N- or C-terminal GFP tags, each under the control of the rme-6 promoter. Expression of these RME-6 fusion proteins fully rescues the coelomocyte endocytosis defect of rme-6(b1014), indicating that both GFP fusions are functional and are very likely to be correctly localized.
PatternGFP-RME-6 was expressed in many tissues, including coelomocytes, oocytes, hypodermis, intestinal and pharyngeal cells.
ReferenceWBPaper00025193
TransgeneWBTransgene00001781