Abstract

Embryos of the sea urchin, Stronglyocentrotus purpuratus, synthesize several classes of sulfated and non-sulfated glycoproteins during gastrulation. The antibiotic tunicamycin, which is a specific inhibitor of the N-glycosylation of proteins, inhibits the synthesis of lipid-linked oligosaccharides in these embryos at concentrations which have little effect on the biosynthesis of other classes of glycolipids or on protein synthesis. As a consequence of this inhibition, glycoproteins with oligosaccharide side chains of the general type (Man)5-7-(GlcNAc)2 are not synthesized. In addition, the biosynthesis of a novel class of sulfated glycoproteins is inhibited. In contrast, no effect upon the synthesis of sulfated glycosaminoglycans is seen. The morphogenetic consequence of tunicamycin treatment is that development of embryos from the mesenchyme blastula to the gastrula stage is arrested. The results provide evidence that during development glycoproteins containing both unsulfated and sulfated N-glycosidically linked oligosaccharide chains are synthesized via the lipid-linked pathway. The biosynthesis of these molecules appears to be a prerequisite to the differentiation and morphogenesis that occurs during gastrulation.

Highlights

  • Embryos of the sea urchin, Strongylocentrotus purpumtus, synthesize several classes of sulfated and nonsulfated glycoproteins during gastrulation

  • The results provide evidence that during development glycoproteins containing both unsulfated and sulfated N-glycosiditally linked oligosaccharide chains are synthesized via the lipid-linked pathway

  • The biosynthesis of these molecules appears to be a prerequisite to the differentiation and morphogenesis that occurs during gastrulation

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Summary

Introduction

Embryos of the sea urchin, Strongylocentrotus purpumtus, synthesize several classes of sulfated and nonsulfated glycoproteins during gastrulation. The results provide evidence that during development glycoproteins containing both unsulfated and sulfated N-glycosiditally linked oligosaccharide chains are synthesized via the lipid-linked pathway. The biosynthesis of these molecules appears to be a prerequisite to the differentiation and morphogenesis that occurs during gastrulation. Interactions of the filopodia of mesenchyme cells with specific cell surface sites are believed to play a role in the migratory and morphogenetic movements [3] that culminate in gastrulation. During this migratory process these embryonic cells acquire an increased negative surface charge [4]. Enhanced incorporation of [“5S]Os during development has been correlated with changes in intercellular adhesions and movements of mesenchyme cells within the embryo [7]

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