Abstract
Defects in glycosaminoglycan biosynthesis disrupt animal development and can cause human disease. So far much of the focus on glycosaminoglycans has been on heparan sulphate. Mutations in eight squashed vulva (sqv) genes in Caenorhabditis elegans cause defects in cytokinesis during embryogenesis and in vulval morphogenesis during postembryonic development. Seven of the eight sqv genes have been shown to control the biosynthesis of the glycosaminoglycans chondroitin and heparan sulphate. Here we present the molecular identification and characterization of the eighth gene, sqv-5. This gene encodes a bifunctional glycosyltransferase that is probably localized to the Golgi apparatus and is responsible for the biosynthesis of chondroitin but not heparan sulphate. Our findings show that chondroitin is crucial for both cytokinesis and morphogenesis during C. elegans development.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alleles
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Amino Acid Sequence
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Animals
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Caenorhabditis elegans / embryology*
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Caenorhabditis elegans / enzymology
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Caenorhabditis elegans / genetics
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Caenorhabditis elegans / metabolism*
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Caenorhabditis elegans Proteins / analysis
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Caenorhabditis elegans Proteins / chemistry
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Caenorhabditis elegans Proteins / genetics
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Caenorhabditis elegans Proteins / metabolism
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Chondroitin / biosynthesis*
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Cloning, Molecular
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Female
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Gene Deletion
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Gene Expression Profiling
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Glycosyltransferases / analysis
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Glycosyltransferases / chemistry
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Glycosyltransferases / genetics
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Glycosyltransferases / metabolism
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Heparitin Sulfate / biosynthesis
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Molecular Sequence Data
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Morphogenesis*
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Sequence Alignment
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Substrate Specificity
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Vulva / embryology*
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Vulva / enzymology
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Vulva / metabolism*
Substances
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Caenorhabditis elegans Proteins
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Chondroitin
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Heparitin Sulfate
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Glycosyltransferases
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sqv-5 protein, C elegans