Maeda Megumi, Kimura Yoshinobu
Functional Glycobiochemistry, Department of Biofunctional Chemistry, Graduate School of Environmental and Life Science, Okayama University Okayama, Japan.
Front Plant Sci. 2014 Sep 4;5:429. doi: 10.3389/fpls.2014.00429. eCollection 2014.
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.
游离N-聚糖(FNGs)在植物细胞的分化、生长和成熟阶段以微摩尔浓度存在。据推测,这些FNGs是参与植物发育或果实成熟的信号分子。然而,FNGs的假设生化和分子功能尚未确定。在植物组织如胚轴、叶片、根、发育中的种子或果实中普遍存在的FNGs结构可分为两种类型:高甘露糖型和植物复合型;前者在大多数情况下,还原端只有一个GlcNAc残基(GN1型),而后者在还原端有壳二糖基单元(GN2型)。这些发现表明,内切-β-N-乙酰葡糖胺酶(ENGase)必定参与GN1型FNGs的产生,而只有肽:N-聚糖酶(PNGase)参与GN2型FNGs的产生。据推测,动物细胞中的胞质PNGase(cPNGase)和ENGase参与高甘露糖型FNGs的产生,以便在蛋白质质量控制系统中从错误折叠的糖蛋白中释放N-聚糖。就植物而言,众所周知,另一种类型的PNGase,即酸性PNGase(aPNGase),在酸性细胞器中参与植物复合型FNGs的产生,这表明植物中的去N-糖基化机制与动物细胞不同。为了更好地理解这些FNGs在植物中的作用,首先鉴定了编码这些N-聚糖释放酶(ENGase和PNGase)的基因,然后分析了ENGase基因敲除植物中FNGs的结构。这些转基因植物为植物特异性去N-糖基化机制和FNGs的假定生理功能提供了新的见解。在这篇综述中,我们重点关注植物FNGs的结构特征,以及cPNGase/ENGase和植物特异性PNGase的功能特征,并讨论了FNGs的假定功能。