Biometals and glycosylation in humans: Congenital disorders of glycosylation shed lights into the crucial role of Golgi manganese homeostasis

About half of the eukaryotic proteins bind biometals that participate in their structure and functions in virtually all physiological processes, including glycosylation. After reviewing the biological roles and transport mechanisms of calcium, magnesium, manganese, zinc and cobalt acting as cofactor...

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Published inBiochimica et biophysica acta. General subjects Vol. 1864; no. 10; p. 129674
Main Authors Foulquier, François, Legrand, Dominique
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.10.2020
Elsevier
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Summary:About half of the eukaryotic proteins bind biometals that participate in their structure and functions in virtually all physiological processes, including glycosylation. After reviewing the biological roles and transport mechanisms of calcium, magnesium, manganese, zinc and cobalt acting as cofactors of the metalloproteins involved in sugar metabolism and/or glycosylation, the paper will outline the pathologies resulting from a dysregulation of these metals homeostasis and more particularly Congenital Disorders of Glycosylation (CDGs) caused by ion transporter defects. Highlighting of CDGs due to defects in SLC39A8 (ZIP8) and TMEM165, two proteins transporting manganese from the extracellular space to cytosol and from cytosol to the Golgi lumen, respectively, has emphasized the importance of manganese homeostasis for glycosylation. Based on our current knowledge of TMEM165 structure and functions, this review will draw a picture of known and putative mechanisms regulating manganese homeostasis in the secretory pathway. •Panorama of biometals essential in glycosylation process.•Diseases resulting from disturbances in biometals homeostasis.•Link between Mn homeostasis and CDG.
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ISSN:0304-4165
1872-8006
1872-8006
DOI:10.1016/j.bbagen.2020.129674