Literature DB >> 24352591

Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains.

Jyoji Morise1, Yasuhiko Kizuka, Keiko Yabuno, Yasuhiro Tonoyama, Noritaka Hashii, Nana Kawasaki, Hiroshi Manya, Yuko Miyagoe-Suzuki, Shin'ichi Takeda, Tamao Endo, Nobuaki Maeda, Hiromu Takematsu, Shogo Oka.   

Abstract

The human natural killer-1 (HNK-1) carbohydrate comprising a sulfated trisaccharide (HSO3-3GlcAβ1-3Galβ1-4GlcNAc-) is expressed on N-linked and O-mannose-linked glycans in the nervous system and involved in learning and memory functions. Although whole/core glycan structures and carrier glycoproteins for the N-linked HNK-1 epitope have been studied, carrier glycoproteins and the biosynthetic pathway of the O-mannose-linked HNK-1 epitope have not been fully characterized. Here, using mass spectrometric analyses, we identified the major carrier glycoprotein of the O-linked HNK-1 as phosphacan in developing mouse brains and determined the major O-glycan structures having the terminal HNK-1 epitope from partially purified phosphacan. The O-linked HNK-1 epitope on phosphacan almost disappeared due to the knockout of protein O-mannose β1,2-N-acetylglucosaminyltransferase 1, an N-acetylglucosaminyltransferase essential for O-mannose-linked glycan synthesis, indicating that the reducing terminal of the O-linked HNK-1 is mannose. We also showed that glucuronyltransferase-P (GlcAT-P) was involved in the biosynthesis of O-mannose-linked HNK-1 using the gene-deficient mice of GlcAT-P, one of the glucuronyltransferases for HNK-1 synthesis. Consistent with this result, we revealed that GlcAT-P specifically synthesized O-linked HNK-1 onto phosphacan using cultured cells. Furthermore, we characterized the as-yet-unknown epitope of the 6B4 monoclonal antibody (mAb), which was thought to recognize a unique phosphacan glycoform. The reactivity of the 6B4 mAb almost completely disappeared in GlcAT-P-deficient mice, and exogenously expressed phosphacan was selectively recognized by the 6B4 mAb when co-expressed with GlcAT-P, suggesting that the 6B4 mAb preferentially recognizes O-mannose-linked HNK-1 on phosphacan. This is the first study to show that 6B4 mAb-reactive O-mannose-linked HNK-1 in the brain is mainly carried by phosphacan.

Entities:  

Keywords:  HNK-1; O-mannose; glucuronyltransferase-P; phosphacan

Mesh:

Substances:

Year:  2013        PMID: 24352591     DOI: 10.1093/glycob/cwt116

Source DB:  PubMed          Journal:  Glycobiology        ISSN: 0959-6658            Impact factor:   4.313


  11 in total

Review 1.  Recent advancements in understanding mammalian O-mannosylation.

Authors:  M Osman Sheikh; Stephanie M Halmo; Lance Wells
Journal:  Glycobiology       Date:  2017-09-01       Impact factor: 4.313

2.  Neurons and glia modify receptor protein-tyrosine phosphatase ζ (RPTPζ)/phosphacan with cell-specific O-mannosyl glycans in the developing brain.

Authors:  Chrissa A Dwyer; Toshihiko Katoh; Michael Tiemeyer; Russell T Matthews
Journal:  J Biol Chem       Date:  2015-03-03       Impact factor: 5.157

3.  HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan.

Authors:  M Osman Sheikh; David Venzke; Mary E Anderson; Takako Yoshida-Moriguchi; John N Glushka; Alison V Nairn; Melina Galizzi; Kelley W Moremen; Kevin P Campbell; Lance Wells
Journal:  Glycobiology       Date:  2020-09-28       Impact factor: 4.313

4.  Targeted release and fractionation reveal glucuronylated and sulphated N- and O-glycans in larvae of dipteran insects.

Authors:  Simone Kurz; Kazuhiro Aoki; Chunsheng Jin; Niclas G Karlsson; Michael Tiemeyer; Iain B H Wilson; Katharina Paschinger
Journal:  J Proteomics       Date:  2015-06-03       Impact factor: 4.044

5.  Role of Site-Specific N-Glycans Expressed on GluA2 in the Regulation of Cell Surface Expression of AMPA-Type Glutamate Receptors.

Authors:  Yusuke Takeuchi; Jyoji Morise; Ippei Morita; Hiromu Takematsu; Shogo Oka
Journal:  PLoS One       Date:  2015-08-13       Impact factor: 3.240

6.  A Sulfated Glycosaminoglycan Linkage Region is a Novel Type of Human Natural Killer-1 (HNK-1) Epitope Expressed on Aggrecan in Perineuronal Nets.

Authors:  Keiko Yabuno; Jyoji Morise; Yasuhiko Kizuka; Noritaka Hashii; Nana Kawasaki; Satoru Takahashi; Shinji Miyata; Tomomi Izumikawa; Hiroshi Kitagawa; Hiromu Takematsu; Shogo Oka
Journal:  PLoS One       Date:  2015-12-10       Impact factor: 3.240

Review 7.  Mammalian O-mannosylation pathway: glycan structures, enzymes, and protein substrates.

Authors:  Jeremy L Praissman; Lance Wells
Journal:  Biochemistry       Date:  2014-05-07       Impact factor: 3.162

Review 8.  3D Structure and Function of Glycosyltransferases Involved in N-glycan Maturation.

Authors:  Masamichi Nagae; Yoshiki Yamaguchi; Naoyuki Taniguchi; Yasuhiko Kizuka
Journal:  Int J Mol Sci       Date:  2020-01-09       Impact factor: 5.923

9.  Mammalian brain glycoproteins exhibit diminished glycan complexity compared to other tissues.

Authors:  Sarah E Williams; Maxence Noel; Sylvain Lehoux; Murat Cetinbas; Ramnik J Xavier; Ruslan I Sadreyev; Edward M Scolnick; Jordan W Smoller; Richard D Cummings; Robert G Mealer
Journal:  Nat Commun       Date:  2022-01-12       Impact factor: 17.694

Review 10.  Keratan sulfate, a complex glycosaminoglycan with unique functional capability.

Authors:  Bruce Caterson; James Melrose
Journal:  Glycobiology       Date:  2018-04-01       Impact factor: 4.313

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