| Literature DB >> 26001781 |
Jae Yong Yoo1, Ki Seong Ko1, Hyun-Kyeong Seo2, Seongha Park2, Wahyu Indra Duwi Fanata1, Rikno Harmoko1, Nirmal Kumar Ramasamy1, Thiyagarajan Thulasinathan1, Tesfaye Mengiste3, Jae-Min Lim2, Sang Yeol Lee1, Kyun Oh Lee4.
Abstract
The most abundant N-glycan in plants is the paucimannosidic N-glycan with core β1,2-xylose and α1,3-fucose residues (Man3XylFuc(GlcNAc)2). Here, we report a mechanism in Arabidopsis thaliana that efficiently produces the largest N-glycan in plants. Genetic and biochemical evidence indicates that the addition of the 6-arm β1,2-GlcNAc residue by N-acetylglucosaminyltransferase II (GnTII) is less effective than additions of the core β1,2-xylose and α1,3-fucose residues by XylT, FucTA, and FucTB in Arabidopsis. Furthermore, analysis of gnt2 mutant and 35S:GnTII transgenic plants shows that the addition of the 6-arm non-reducing GlcNAc residue to the common N-glycan acceptor GlcNAcMan3(GlcNAc)2 inhibits additions of the core β1,2-xylose and α1,3-fucose residues. Our findings indicate that plants limit the rate of the addition of the 6-arm GlcNAc residue to the common N-glycan acceptor as a mechanism to facilitate formation of the prevalent N-glycans with Man3XylFuc(GlcNAc)2 and (GlcNAc)2Man3XylFuc(GlcNAc)2 structures.Entities:
Keywords: carbohydrate processing; glycosylation; glycosyltransferase; plant; post-translational modification (PTM)
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Year: 2015 PMID: 26001781 PMCID: PMC4505410 DOI: 10.1074/jbc.M115.653162
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157