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Heritable disorders in the metabolism of the dolichols: A bridge from sterol biosynthesis to molecular glycosylation.


ABSTRACT: Dolichols, polyisoprene alcohols derived from the mevalonate pathway of cholesterol synthesis, serve as carriers of glycan precursors for the formation of oligosaccharides important in protein glycosylation. Seven autosomal-recessively inherited disorders in the metabolism (synthesis, utilization, recycling) of the dolichols have recently been described, and all are associated with decreased lipid-linked oligosaccharides leading to underglycosylated proteins or lipids which facilitate their detection in the diagnostic laboratory. Multisystem pathology encompasses developmental delays and eye, heart, skin and muscle abnormalities; outcomes range from death in infancy to mild, late-onset disease.

SUBMITTER: Wolfe LA 

PROVIDER: S-EPMC3995744 | biostudies-other | 2012 Nov

REPOSITORIES: biostudies-other

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Heritable disorders in the metabolism of the dolichols: A bridge from sterol biosynthesis to molecular glycosylation.

Wolfe Lynne A LA   Morava Eva E   He Miao M   Vockley Jerry J   Gibson K Michael KM  

American journal of medical genetics. Part C, Seminars in medical genetics 20121011 4


Dolichols, polyisoprene alcohols derived from the mevalonate pathway of cholesterol synthesis, serve as carriers of glycan precursors for the formation of oligosaccharides important in protein glycosylation. Seven autosomal-recessively inherited disorders in the metabolism (synthesis, utilization, recycling) of the dolichols have recently been described, and all are associated with decreased lipid-linked oligosaccharides leading to underglycosylated proteins or lipids which facilitate their dete  ...[more]

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