Secreted Wingless-interacting molecule (Swim) promotes long-range signaling by maintaining Wingless solubility |
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Authors: | Mulligan Kimberly A Fuerer Christophe Ching Wendy Fish Matt Willert Karl Nusse Roeland |
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Affiliation: | The Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA. |
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Abstract: | Lipid-modified Wnt/Wingless (Wg) proteins can signal to their target cells in a short- or long-range manner. How these hydrophobic proteins travel through the extracellular environment remains an outstanding question. Here, we report on a Wg binding protein, Secreted Wg-interacting molecule (Swim), that facilitates Wg diffusion through the extracellular matrix. Swim, a putative member of the Lipocalin family of extracellular transport proteins, binds to Wg with nanomolar affinity in a lipid-dependent manner. In quantitative signaling assays, Swim is sufficient to maintain the solubility and activity of purified Wg. In Drosophila, swim RNAi phenotypes resemble wg loss-of-function phenotypes in long-range signaling. We propose that Swim is a cofactor that promotes long-range Wg signaling in vivo by maintaining the solubility of Wg. |
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Keywords: | development morphogenesis pattern palmitoylation lipid modification |
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