Journal
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
Volume 83, Issue -, Pages 21-34Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ibmb.2017.02.005
Keywords
Protein glycosylation; Post-translational modifications; Insect glycans; Development; Fucose; Pauci-mannose; CNS
Categories
Funding
- Fund for Scientific Research (FWO-Vlaanderen)
- Research Council of Ghent University
- Agency for Innovation by Science and Technology in Flanders (IWT)
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The majority of proteins is modified with carbohydrate structures. This modification, called glycosylation, was shown to be crucial for protein folding, stability and subcellular location, as well as protein-protein interactions, recognition and signaling. Protein glycosylation is involved in multiple physiological processes, including embryonic development, growth, circadian rhythms, cell attachment as well as maintenance of organ structure, immunity and fertility. Although the general principles of glycosylation are similar among eukaryotic organisms, insects synthesize a distinct repertoire of glycan structures compared to plants and vertebrates. Consequently, a number of unique insect glycans mediate functions specific to this class of invertebrates. For instance, the core alpha 1,3-fucosylation of N-glycans is absent in vertebrates, while in insects this modification is crucial for the development of wings and the nervous system. At present, most of the data on insect glycobiology comes from research in Drosophila. Yet, progressively more information on the glycan structures and the importance of glycosylation in other insects like beetles, caterpillars, aphids and bees is becoming available. This review gives a summary of the current knowledge and recent progress related to glycan diversity and function(s) of protein glycosylation in insects. We focus on N- and O-glycosylation, their synthesis, physiological role(s), as well as the molecular and biochemical basis of these processes. (C) 2017 Elsevier Ltd. All rights reserved.
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