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Biosynthesis of truncated N-linked oligosaccharides results from non-orthologous hexosaminidase-mediated mechanisms in nematodes, plants, and insects
被引:82
作者:
Gutternigg, Martin
Kretschmer-Lubich, Dorothea
Paschinger, Katharina
Rendic, Dubravko
Hader, Josef
Geier, Petra
Ranftl, Ramona
Jantsch, Verena
Lochnit, Guenter
Wilson, Iain B. H.
机构:
[1] Univ Nat Resources & Appl Life Sci, Dept Chem, BOKU, A-1190 Vienna, Austria
[2] Vienna Bioctr 2, Abt Chromosomenbiol, A-1030 Vienna, Austria
[3] Univ Giessen, Inst Biochem, D-35292 Giessen, Germany
基金:
奥地利科学基金会;
关键词:
D O I:
10.1074/jbc.M704235200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In many invertebrates and plants, the N-glycosylation profile is dominated by truncated paucimannosidic N-glycans, i.e. glycans consisting of a simple trimannosylchitobiosyl core often modified by core fucose residues. Even though they lack antennal N-acetylglucosamine residues, the biosynthesis of these glycans requires the sequential action of GlcNAc transferase I, Golgi mannosidase II, and, finally, beta-N-acetylglucosaminidases. In Drosophila, the recently characterized enzyme encoded by the fused lobes (fdl) gene specifically removes the non-reducing N-acetylglucosamine residue from the alpha 1,3-antenna of N-glycans. In the present study, we examined the products of five beta-N-acetylhexosaminidase genes from Caenorhabditis elegans (hex-1 to hex-5, corresponding to reading frames T14F9.3, C14C11.3, Y39A1C.4, Y51F10.5, and Y70D2A.2) in addition to three from Arabidopsis thaliana (AtHEX1, AtHEX2, and AtHEX3, corresponding to reading frames At1g65590, At3g55260, and At1g05590). Based on homology, the Caenorhabditis HEX-1 and all three Arabidopsis enzymes are members of the same sub-family as the aforementioned Drosophila fused lobes enzyme but either act as chitotriosidases or non-specifically remove N-acetylglucosamine from both N-glycan antennae. The other four Caenorhabditis enzymes are members of a distinct sub-family; nevertheless, two of these enzymes displayed the same alpha 1,3-antennal specificity as the fused lobes enzyme. Furthermore, a deletion of part of the Caenorhabditis hex-2 gene drastically reduces the native N-glycan-specific hexosaminidase activity in mutant worm extracts and results in a shift in the N-glycan profile, which is a demonstration of its in vivo enzymatic relevance. Based on these data, it is hypothesized that the genetic origin of pauci-mannosidic glycans in nematodes, plants, and insects involves highly divergent members of the same hexosaminidase gene family.
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页码:27825 / 27840
页数:16
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