Literature DB >> 18430784

In vivo role of lipid adducts on Wingless.

Xavier Franch-Marro1, Franz Wendler, Janice Griffith, Madelon M Maurice, Jean-Paul Vincent.   

Abstract

Two lipids (palmitate and palmitoleic acid) are appended onto Wnt proteins. It has been suggested that palmitate is required for signalling, whereas palmitoleic acid is necessary for progression through the secretory pathway. By mutating the relevant amino acids, we have investigated how these adducts contribute to the secretion and signalling activity of Wingless, the main Drosophila member of the Wnt family. Analysis of Wingless with a Cysteine 93 to Alanine mutation ([C93A]Wingless) shows that palmitoylation is essential for signalling activity in vivo (as well as in cultured cells). Moreover, without palmitate, Wingless fails to reach the surface of imaginal disc cells and, as electron microscopy (EM) analysis suggests, appears to accumulate in the endoplasmic reticulum (ER). Artificial targeting of palmitate-deficient Wingless to the plasma membrane does not rescue signalling activity. Therefore, palmitate at C93 has a dual role: in secretion and signalling. From our analysis of [S239A]Wingless, which lacks a conserved residue shown to be acylated in Wnt3a, we infer that palmitoleic acid is not, as previously suggested, absolutely required for secretion. Nevertheless, this mutant has poor signalling activity, suggesting that palmitoleic acid contributes significantly to signalling. We suggest that the overall level of lipidation affects signalling activity.

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Year:  2008        PMID: 18430784     DOI: 10.1242/jcs.015958

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  31 in total

1.  Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation.

Authors:  Xinjun Zhang; Jose Garcia Abreu; Chika Yokota; Bryan T MacDonald; Sasha Singh; Karla Loureiro Almeida Coburn; Seong-Moon Cheong; Mingzi M Zhang; Qi-Zhuang Ye; Howard C Hang; Hanno Steen; Xi He
Journal:  Cell       Date:  2012-06-22       Impact factor: 41.582

2.  Roles of N-glycosylation and lipidation in Wg secretion and signaling.

Authors:  Xiaofang Tang; Yihui Wu; Tatyana Y Belenkaya; Qinzhu Huang; Lorraine Ray; Jia Qu; Xinhua Lin
Journal:  Dev Biol       Date:  2012-01-21       Impact factor: 3.582

Review 3.  Wnt signaling from development to disease: insights from model systems.

Authors:  Ken M Cadigan; Mark Peifer
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-08       Impact factor: 10.005

Review 4.  Wnt/beta-catenin signaling: components, mechanisms, and diseases.

Authors:  Bryan T MacDonald; Keiko Tamai; Xi He
Journal:  Dev Cell       Date:  2009-07       Impact factor: 12.270

5.  Non-acylated Wnts Can Promote Signaling.

Authors:  Kelsey F Speer; Anselm Sommer; Benjamin Tajer; Mary C Mullins; Peter S Klein; Mark A Lemmon
Journal:  Cell Rep       Date:  2019-01-22       Impact factor: 9.423

Review 6.  Palmitoylation of Hedgehog proteins.

Authors:  John A Buglino; Marilyn D Resh
Journal:  Vitam Horm       Date:  2012       Impact factor: 3.421

Review 7.  Extracellular movement of signaling molecules.

Authors:  Patrick Müller; Alexander F Schier
Journal:  Dev Cell       Date:  2011-07-19       Impact factor: 12.270

8.  env1 Mutant of VPS35 gene exhibits unique protein localization and processing phenotype at Golgi and lysosomal vacuole in Saccharomyces cerevisiae.

Authors:  Editte Gharakhanian; Onyinyechi Chima-Okereke; Daniel K Olson; Christopher Frost; M Kathleen Takahashi
Journal:  Mol Cell Biochem       Date:  2010-10-10       Impact factor: 3.396

Review 9.  Lipid-modified morphogens: functions of fats.

Authors:  Josefa Steinhauer; Jessica E Treisman
Journal:  Curr Opin Genet Dev       Date:  2009-05-11       Impact factor: 5.578

10.  Active Wnt proteins are secreted on exosomes.

Authors:  Julia Christina Gross; Varun Chaudhary; Kerstin Bartscherer; Michael Boutros
Journal:  Nat Cell Biol       Date:  2012-09-16       Impact factor: 28.824

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