Biosynthesis, Post-translation Modification, and Functional Characterization of Drm/Gremlin - Archive ouverte HAL
Article Dans Une Revue Journal of Biological Chemistry Année : 2000

Biosynthesis, Post-translation Modification, and Functional Characterization of Drm/Gremlin

Résumé

Down-regulated by mos (Drm)/Gremlin is a highly conserved protein whose properties and expression pattern suggest a role in early development, tissue-specific differentiation, and cell transformation. We have investigated the biosynthesis and processing of Drm expressed endogenously in rat fibroblasts or overexpressed following transient or stable transfection. Analysis of metabolically labeled cells revealed that Drm exists in secreted and cell-associated forms that exhibit similar mobilities in SDS-polyacrylamide gel electrophoresis. Protein analysis indicated that Drm is present in two major species: a slow migrating glycosylated form and a nonglycosylated form. Both forms of Drm are able to undergo phosphorylation. Drm is released into the media within 30 min of synthesis and is detectable for up to 4-5 h, whereas the cell-associated form has a half-life of about 1 h. Confocal immunofluorescent microscopy indicates that Drm is present both on the external surface of expressing cells, as well as within the endoplasmic reticulum and the Golgi. Both glycosylated and nonglycosylated forms of Drm exhibit identical distributions and are able to antagonize bone morphogenetic protein signaling. Like the soluble form, the cell-associated forms are capable of binding (125)I-bone morphogenetic protein-4. These properties are consistent with a role for Drm in interfering with signaling and indicate that Drm may act at the cell surface during tissue development and transformation.

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Dates et versions

hal-04717460 , version 1 (01-10-2024)

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Citer

Lilia Topol, Boris Bardot, Qingyun Zhang, James Resau, Emmanuelle Huillard, et al.. Biosynthesis, Post-translation Modification, and Functional Characterization of Drm/Gremlin. Journal of Biological Chemistry, 2000, 275 (12), pp.8785-8793. ⟨10.1074/jbc.275.12.8785⟩. ⟨hal-04717460⟩

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