The intracellular concentration of sialic acid regulates the polysialylation of the neural cell adhesion molecule |
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Authors: | Bork Kaya Reutter Werner Gerardy-Schahn Rita Horstkorte Rüdiger |
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Affiliation: | Institut für Biochemie und Molekularbiologie, Charité-Universit?tsmedizin Berlin, Campus Benjamin Franklin, Arnimallee 22, 14195 Berlin-Dahlem, Germany. |
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Abstract: | Sialic acids are expressed as terminal sugars in many glycoconjugates and play an important role during development and regeneration, as they are involved as polysialic acid in a variety of cell-cell interactions mediated by the neural cell adhesion molecule NCAM. The key enzyme for the biosynthesis of sialic acid is the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine-kinase (GNE). Mutations in the binding site of the feedback inhibitor CMP-sialic acid of the GNE leads to sialuria, a disease in which patients produce sialic acid in gram scale. Here, we report on the consequences after expression of a sialuria-mutated GNE. Expression of the sialuria-mutated GNE leads to a dramatic increase of both cellular sialic acid and polysialic acid on NCAM. This could also be achieved by application of the sialic acid precursor N-acetylmannosamine. Our data suggest that biosynthesis of sialic acid regulates and limits the synthesis of polysialic acid. |
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Keywords: | UDP-N-Acetylglucosamine 2-epimerase/N-acetylmannosaminekinase N-Acetylmannosamine |
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