Limited Addition of the 6-Arm beta 1,2-linked N-Acetylglucosamine (GlcNAc) Residue Facilitates the Formation of the Largest N-Glycan in Plantsopen access
- Authors
- Yoo, Jae Yong; Ko, Ki Seong; Seo, Hyun-Kyeong; Park, Seongha; Fanata, Wahyu Indra Duwi; Harmoko, Rikno; Ramasamy, Nirmal Kumar; Thulasinathan, Thiyagarajan; Mengiste, Tesfaye; Lim, Jae-Min; Lee, Sang Yeol; Lee, Kyun Oh
- Issue Date
- 3-Jul-2015
- Publisher
- AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
- Citation
- JOURNAL OF BIOLOGICAL CHEMISTRY, v.290, no.27, pp 16560 - 16572
- Pages
- 13
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF BIOLOGICAL CHEMISTRY
- Volume
- 290
- Number
- 27
- Start Page
- 16560
- End Page
- 16572
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/17126
- DOI
- 10.1074/jbc.M115.653162
- ISSN
- 0021-9258
1083-351X
- Abstract
- The most abundant N-glycan in plants is the paucimannosidic N-glycan with core beta 1,2-xylose and alpha 1,3-fucose residues (Man(3)XylFuc(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 beta 1,2-GlcNAc residue by N-acetylglucosaminyltransferase II (GnTII) is less effective than additions of the core beta 1,2-xylose and alpha 1,3-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 GlcNAcMan(3)(GlcNAc)(2) inhibits additions of the core beta 1,2-xylose and alpha 1,3-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 Man(3)XylFuc(GlcNAc)(2) and (GlcNAc)(2)Man(3)XylFuc(GlcNAc)(2) structures.
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