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O-methylated N-glycans Distinguish Mosses from Vascular Plants
In the animal kingdom, a stunning variety of N-glycan structures have emerged with phylogenetic specificities of various kinds. In the plant kingdom, however, N-glycosylation appears to be strictly conservative and uniform. From mosses to all kinds of gymno- and angiosperms, land plants mainly expre...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773788/ https://www.ncbi.nlm.nih.gov/pubmed/35053284 http://dx.doi.org/10.3390/biom12010136 |
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author | Stenitzer, David Mócsai, Réka Zechmeister, Harald Reski, Ralf Decker, Eva L. Altmann, Friedrich |
author_facet | Stenitzer, David Mócsai, Réka Zechmeister, Harald Reski, Ralf Decker, Eva L. Altmann, Friedrich |
author_sort | Stenitzer, David |
collection | PubMed |
description | In the animal kingdom, a stunning variety of N-glycan structures have emerged with phylogenetic specificities of various kinds. In the plant kingdom, however, N-glycosylation appears to be strictly conservative and uniform. From mosses to all kinds of gymno- and angiosperms, land plants mainly express structures with the common pentasaccharide core substituted with xylose, core α1,3-fucose, maybe terminal GlcNAc residues and Lewis A determinants. In contrast, green algae biosynthesise unique and unusual N-glycan structures with uncommon monosaccharides, a plethora of different structures and various kinds of O-methylation. Mosses, a group of plants that are separated by at least 400 million years of evolution from vascular plants, have hitherto been seen as harbouring an N-glycosylation machinery identical to that of vascular plants. To challenge this view, we analysed the N-glycomes of several moss species using MALDI-TOF/TOF, PGC-MS/MS and GC-MS. While all species contained the plant-typical heptasaccharide with no, one or two terminal GlcNAc residues (MMXF, MGnXF and GnGnXF, respectively), many species exhibited MS signals with 14.02 Da increments as characteristic for O-methylation. Throughout all analysed moss N-glycans, the level of methylation differed strongly even within the same family. In some species, methylated glycans dominated, while others had no methylation at all. GC-MS revealed the main glycan from Funaria hygrometrica to contain 2,6-O-methylated terminal mannose. Some mosses additionally presented very large, likewise methylated complex-type N-glycans. This first finding of the methylation of N-glycans in land plants mirrors the presumable phylogenetic relation of mosses to green algae, where the O-methylation of mannose and many other monosaccharides is a common trait. |
format | Online Article Text |
id | pubmed-8773788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87737882022-01-21 O-methylated N-glycans Distinguish Mosses from Vascular Plants Stenitzer, David Mócsai, Réka Zechmeister, Harald Reski, Ralf Decker, Eva L. Altmann, Friedrich Biomolecules Article In the animal kingdom, a stunning variety of N-glycan structures have emerged with phylogenetic specificities of various kinds. In the plant kingdom, however, N-glycosylation appears to be strictly conservative and uniform. From mosses to all kinds of gymno- and angiosperms, land plants mainly express structures with the common pentasaccharide core substituted with xylose, core α1,3-fucose, maybe terminal GlcNAc residues and Lewis A determinants. In contrast, green algae biosynthesise unique and unusual N-glycan structures with uncommon monosaccharides, a plethora of different structures and various kinds of O-methylation. Mosses, a group of plants that are separated by at least 400 million years of evolution from vascular plants, have hitherto been seen as harbouring an N-glycosylation machinery identical to that of vascular plants. To challenge this view, we analysed the N-glycomes of several moss species using MALDI-TOF/TOF, PGC-MS/MS and GC-MS. While all species contained the plant-typical heptasaccharide with no, one or two terminal GlcNAc residues (MMXF, MGnXF and GnGnXF, respectively), many species exhibited MS signals with 14.02 Da increments as characteristic for O-methylation. Throughout all analysed moss N-glycans, the level of methylation differed strongly even within the same family. In some species, methylated glycans dominated, while others had no methylation at all. GC-MS revealed the main glycan from Funaria hygrometrica to contain 2,6-O-methylated terminal mannose. Some mosses additionally presented very large, likewise methylated complex-type N-glycans. This first finding of the methylation of N-glycans in land plants mirrors the presumable phylogenetic relation of mosses to green algae, where the O-methylation of mannose and many other monosaccharides is a common trait. MDPI 2022-01-15 /pmc/articles/PMC8773788/ /pubmed/35053284 http://dx.doi.org/10.3390/biom12010136 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Stenitzer, David Mócsai, Réka Zechmeister, Harald Reski, Ralf Decker, Eva L. Altmann, Friedrich O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title | O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title_full | O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title_fullStr | O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title_full_unstemmed | O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title_short | O-methylated N-glycans Distinguish Mosses from Vascular Plants |
title_sort | o-methylated n-glycans distinguish mosses from vascular plants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773788/ https://www.ncbi.nlm.nih.gov/pubmed/35053284 http://dx.doi.org/10.3390/biom12010136 |
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