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Updated: Jul 18, 2026

Detection of Small GTPase Prenylation and GTP Binding Using Membrane Fractionation and GTPase-linked Immunosorbent Assay
Published on: November 11, 2018
Sprinter: a novel transmembrane protein required for Wg secretion and signaling
Robyn M Goodman1, Shreya Thombre, Zeynep Firtina
1University of Delaware, Department of Biological Sciences, Newark DE, USA.
Abstract:
Wingless (Wg) is a secreted ligand that differentially activates gene expression in target tissues. It belongs to the Wnt family of secreted signaling molecules that regulate cell-to-cell interactions during development. Activation of Wg targets is dependent on the ligand concentration in the extracellular milieu; cellular mechanisms that govern the synthesis, delivery and receipt of Wg are elaborate and complex. We have identified sprinter (srt), which encodes a novel, evolutionarily conserved transmembrane protein required for the transmission of the Wg signal. Mutations in srt cause the accumulation of Wg in cells that express it, and retention of the ligand prevents activation of its target genes in signal-receiving cells. In the absence of Srt activity, levels of Wg targets (including Engrailed in embryos lacking maternal and zygotic srt, and Senseless and Achaete in wing discs) are reduced. Activation of Wg targets in the receiving cells does not require srt. Hence, the function of Srt is restricted to events occurring within the Wg-producing cells. We show that srt is not required for any aspect of Hedgehog (Hh) signal transduction, suggesting specificity of srt for the Wg pathway. We propose that srt encodes a protein required for Wg secretion that regulates maturation, membrane targeting or delivery of Wg. Loss of srt function in turn diminishes Wg-pathway activation in receiving cells.
Insights
The novel sprinter (srt) protein is essential for Wingless (Wg) secretion from producing cells. Loss of srt function prevents Wg signaling, impacting target gene activation during development.
Area of Science:
- Developmental Biology
- Cell Signaling
- Molecular Genetics
Background:
- Wingless (Wg) is a crucial secreted ligand in the Wnt family, regulating cell-to-cell interactions and gene expression during development.
- Wg signaling pathway activation is dependent on extracellular ligand concentration, involving complex cellular mechanisms for synthesis, delivery, and reception.
- Understanding the precise mechanisms of Wg secretion and transport is vital for comprehending developmental processes.
Purpose of the Study:
- To identify novel factors involved in the Wingless (Wg) signaling pathway.
- To elucidate the function of the newly identified sprinter (srt) gene in Wg signal transmission.
- To determine the cellular site and specificity of Srt protein action within the Wg pathway.
Main Methods:
- Genetic screens to identify mutations affecting Wg signaling.
- Analysis of Wg target gene expression in mutant embryos and wing discs.
- Characterization of the sprinter (srt) gene and its encoded transmembrane protein.
- Comparative analysis with Hedgehog (Hh) signaling to assess pathway specificity.
Main Results:
- Identification of sprinter (srt) as a gene encoding a novel transmembrane protein essential for Wg signal transmission.
- Mutations in srt lead to the accumulation of Wg within producing cells and reduced Wg target gene activation (Engrailed, Senseless, Achaete).
- Srt function is confined to Wg-producing cells and is specific to the Wg pathway, not affecting Hedgehog signaling.
Conclusions:
- The sprinter (srt) gene product is required for the efficient secretion or release of Wingless (Wg) ligand from producing cells.
- Srt likely plays a role in Wg maturation, membrane targeting, or export, regulating the availability of functional ligand.
- Disruption of Srt function impairs Wg pathway activation in receiving cells due to a lack of secreted Wg.
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