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WormBase Tree Display for Expr_pattern: Expr11880

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Name Class

Expr11880Expression_ofGeneWBGene00004962
Reflects_endogenous_expression_ofWBGene00004962
Expression_dataAnatomy_termWBbt:0006798Certain
WBbt:0006799Certain
GO_termGO:0005886
GO:0005737
Subcellular_localizationSPE-8 localizes to the cell membrane during spermatogenesis. All cellular stages of spermatogenesis showed green fluorescence associated with the cell membrane. Unfortunately, developing sperm cells have autofluorescent internal structures. In comparison, control (non-reporter) developing sperm do not have green fluorescence associated with the cell membrane. The primary spermatocytes expressing the reporter appear much more fluorescent even interior to the cell membrane than N2 controls, suggesting that SPE-8 may be accumulating in the cytosol and translocating to the membrane at this stage. By the secondary spermatocyte stage, the cytosol appears no more fluorescent than controls, but the plasma membrane is strongly fluorescent as the reporter has taken up residence there. At the budding spermatid stage a strong GFP signal comes from the residual body, where non-essential cellular components are disposed. It is unclear if native SPE-8 enters the residual body, and an alternative possibility is that some of the fusion has degraded and segregated to the residual body. Finally, the membrane localization of GFP is most pronounced at the spermatid stage, when the cells await the activation signal. In naturally activated spermatozoa from both males and hermaphrodites, the membrane localization found in spermatids disperses into the cytoplasm.
TypeReporter_gene
PatternUsing the Mos-SCI technique, two SPE-8::GFP translational fusions were integrated into the ttTi5605 Mos1 transposon insertion on Chromosome II. One fusion had GFP on the N-terminus, and the other had GFP on the C-terminus. Both showed green fluorescence in the male germline.
PictureWBPicture0000013738
RemarkTemporal description
ReferenceWBPaper00045487
TransgeneWBTransgene00020106