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Review
. 2014 Sep 4:5:429.
doi: 10.3389/fpls.2014.00429. eCollection 2014.

Structural features of free N-glycans occurring in plants and functional features of de-N-glycosylation enzymes, ENGase, and PNGase: the presence of unusual plant complex type N-glycans

Affiliations
Review

Structural features of free N-glycans occurring in plants and functional features of de-N-glycosylation enzymes, ENGase, and PNGase: the presence of unusual plant complex type N-glycans

Megumi Maeda et al. Front Plant Sci. .

Abstract

Free N-glycans (FNGs) are present at micromolar concentrations in plant cells during their differentiation, growth, and maturation stages. It has been postulated that these FNGs are signaling molecules involved in plant development or fruit ripening. However, the hypothetical biochemical and molecular function of FNGs has not been yet established. The structure of FNGs found ubiquitously in plant tissues such as hypocotyls, leaves, roots, developing seeds, or fruits can be classified into two types: high-mannose type and plant complex type; the former, in most cases, has only one GlcNAc residue at the reducing end (GN1 type), while the latter has the chitobiosyl unit at the reducing end (GN2 type). These findings suggest that endo-β-N-acetylglucosaminidase (ENGase) must be involved in the production of GN1 type FNGs, whereas only peptide:N-glycanase (PNGase) is involved in the production of GN2 type FNGs. It has been hypothesized that cytosolic PNGase (cPNGase) and ENGase in animal cells are involved in the production of high-mannose type FNGs in order to release N-glycans from the misfolded glycoproteins in the protein quality control systems. In the case of plants, it is well known that another type of PNGase, the acidic PNGase (aPNGase) is involved in the production of plant complex type FNGs in an acidic organelle, suggesting the de-N-glycosylation mechanism in plants is different from that in animal cells. To better understand the role of these FNGs in plants, the genes encoding these N-glycan releasing enzymes (ENGase and PNGase) were first identified, and then structure of FNGs in ENGase knocked-out plants were analyzed. These transgenic plants provide new insight into the plant-specific de-N-glycosylation mechanism and putative physiological functions of FNGs. In this review, we focus on the structural features of plant FNGs, as well as functional features of cPNGase/ENGase and plant specific PNGase, and putative functions of FNGs are also discussed.

Keywords: ENGase; PNGase; free N-glycans; glycochaperone; knockout plant.

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Figures

FIGURE 1
FIGURE 1
Typical structures of plant N-glycans: high-mannose type structure and two kinds of complex type N-glycans.
FIGURE 2
FIGURE 2
Schematic representation of the possible processing pathway of plant N-glycans.
FIGURE 3
FIGURE 3
Typical structures of free N-glycans (FNGs) found in plants. (A) Free N-glycans found in the soluble fraction of rice cells (cytosol and vacuole). (B) Free N-glycans found in culture broth (extracellular space).
FIGURE 4
FIGURE 4
Schematic representation of the putative processing and secretion pathway of plant complex type GN1-FNGs. Retrotransporter for the high-mannose type GN1-FNGs produced in the cytosol has not been identified.
FIGURE 5
FIGURE 5
Phylogenic tree of the acidic PNGase (tomato and A. thaliana): two genetic groups of plant aPNGase. 1)aPNGase-Le; tomato acidic PNGase (Hossain et al., 2010b).

References

    1. Alisi C., Afferni C., Iacovacci P., Barletta B., Tinghino R., Butteroni C., et al. (2001). Rapid isolation, characterization, and glycan analysis of Cup a 1, the major allergen of Arizona cypress (Cupressus arizonica) pollen. Allergy 56 978–984 10.1034/j.1398-9995.2001.103125.x - DOI - PubMed
    1. Altmann F., Paschinger K., Dalik T., Vorauer K. (1998). Characterisation of peptide-N4-(N-acetyl-β-glucosaminyl)asparagine amidase A and its N-glycans. Eur. J. Biochem. 252 118–123 10.1046/j.1432-1327.1998.2520118.x - DOI - PubMed
    1. Boisson M., Gomord V., Audran C., Berger N., Dubreucq D., Granier F., et al. (2001). Arabidopsis glucosidase I mutants reveal a critical role of N-glycan trimming in seed development. EMBO J. 20 1010–1019 10.1093/emboj/20.5.1010 - DOI - PMC - PubMed
    1. Chang T., Kuo M. C., Khoo K. H., Inoue S., Inoue Y. (2000). Developmentally regulated expression of a peptide:N-glycanase during germination of rice seeds (Oryza sativa) and its purification and characterization. J. Biol. Chem. 275 129–134 10.1074/jbc.275.1.129 - DOI - PubMed
    1. Diepold A., Li G., Lennarz W. J., Nürnberger T., Brunner F. (2007). The Arabidopsis AtPNG1 gene encodes a peptide:N-glycanase. Plant J. 52 94–104 10.1111/j.1365-313X.2007.03215.x - DOI - PubMed

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