Literature DB >> 12857818

Glycosylation motifs that direct arabinogalactan addition to arabinogalactan-proteins.

Li Tan1, Joseph F Leykam, Marcia J Kieliszewski.   

Abstract

Hydroxyproline (Hyp)-rich glycoproteins (HRGPs) participate in all aspects of plant growth and development. HRGPs are generally highly O-glycosylated through the Hyp residues, which means carbohydrates help define the interactive molecular surface and, hence, HRGP function. The Hyp contiguity hypothesis predicts that contiguous Hyp residues are sites of HRGP arabinosylation, whereas clustered noncontiguous Hyp residues are sites of galactosylation, giving rise to the arabinogalactan heteropolysaccharides that characterize the arabinogalactan-proteins. Early tests of the hypothesis using synthetic genes encoding only clustered noncontiguous Hyp in the sequence (serine [Ser]-Hyp-Ser-Hyp)(n) or contiguous Hyp in the series (Ser-Hyp-Hyp)(n) and (Ser-Hyp-Hyp-Hyp-Hyp)(n) confirmed that arabinogalactan polysaccharide was added only to noncontiguous Hyp, whereas arabinosylation occurred on contiguous Hyp. Here, we extended our tests of the codes that direct arabinogalactan polysaccharide addition to Hyp by building genes encoding the repetitive sequences (alanine [Ala]-proline [Pro]-Ala-Pro)(n), (threonine [Thr]-Pro-Thr-Pro)(n), and (valine [Val]-Pro-Val-Pro)(n), and expressing them in tobacco (Nicotiana tabacum) Bright-Yellow 2 cells as fusion proteins with green fluorescent protein. All of the Pro residues in the (Ala-Pro-Ala-Pro)(n) fusion protein were hydroxylated and consistent with the hypothesis that every Hyp residue was glycosylated with arabinogalactan polysaccharide. In contrast, 20% to 30% of Pro residues remained non-hydroxylated in the (Thr-Pro-Thr-Pro)(n), and (Val-Pro-Val-Pro)(n) fusion proteins. Furthermore, although 50% to 60% of the Hyp residues were glycosylated with arabinogalactan polysaccharide, some remained non-glycosylated or were arabinosylated. These results suggest that the amino acid side chains of flanking residues influence the extent of Pro hydroxylation and Hyp glycosylation and may explain why isolated noncontiguous Hyp in extensins do not acquire an arabinogalactan polysaccharide but are arabinosylated or remain non-glycosylated.

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Year:  2003        PMID: 12857818      PMCID: PMC167076          DOI: 10.1104/pp.103.021766

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  44 in total

1.  Characterization and expression of four proline-rich cell wall protein genes in Arabidopsis encoding two distinct subsets of multiple domain proteins.

Authors:  T J Fowler; C Bernhardt; M L Tierney
Journal:  Plant Physiol       Date:  1999-12       Impact factor: 8.340

2.  DcAGP1, a secreted arabinogalactan protein, is related to a family of basic proline-rich proteins.

Authors:  T C Baldwin; C Domingo; T Schindler; G Seetharaman; N Stacey; K Roberts
Journal:  Plant Mol Biol       Date:  2001-03       Impact factor: 4.076

3.  Isolation, characterization and immunolocalization of a novel, modular tomato arabinogalactan-protein corresponding to the LeAGP-1 gene.

Authors:  M Gao; M J Kieliszewski; D T Lamport; A M Showalter
Journal:  Plant J       Date:  1999-04       Impact factor: 6.417

4.  Alkaline degradation of polysaccharides.

Authors:  R L WHISTLER; J N BEMILLER
Journal:  Adv Carbohydr Chem       Date:  1958

5.  Glycosylphosphatidylinositol-anchored cell-surface proteins from Arabidopsis.

Authors:  D J Sherrier; T A Prime; P Dupree
Journal:  Electrophoresis       Date:  1999-07       Impact factor: 3.535

6.  Synthetic genes for glycoprotein design and the elucidation of hydroxyproline-O-glycosylation codes.

Authors:  E Shpak; J F Leykam; M J Kieliszewski
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

7.  New method for quantitative determination of uronic acids.

Authors:  N Blumenkrantz; G Asboe-Hansen
Journal:  Anal Biochem       Date:  1973-08       Impact factor: 3.365

8.  The isolation and partial characterization of hydroxyproline-rich glycopeptides obtained by enzymic degradation of primary cell walls.

Authors:  D T Lamport
Journal:  Biochemistry       Date:  1969-03       Impact factor: 3.162

9.  The classical arabinogalactan protein gene family of arabidopsis.

Authors:  C J Schultz; K L Johnson; G Currie; A Bacic
Journal:  Plant Cell       Date:  2000-09       Impact factor: 11.277

Review 10.  Extensin: repetitive motifs, functional sites, post-translational codes, and phylogeny.

Authors:  M J Kieliszewski; D T Lamport
Journal:  Plant J       Date:  1994-02       Impact factor: 6.417

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  48 in total

Review 1.  Arabinogalactan proteins in root and pollen-tube cells: distribution and functional aspects.

Authors:  Eric Nguema-Ona; Sílvia Coimbra; Maïté Vicré-Gibouin; Jean-Claude Mollet; Azeddine Driouich
Journal:  Ann Bot       Date:  2012-07       Impact factor: 4.357

2.  Plant O-hydroxyproline arabinogalactans are composed of repeating trigalactosyl subunits with short bifurcated side chains.

Authors:  Li Tan; Peter Varnai; Derek T A Lamport; Chunhua Yuan; Jianfeng Xu; Feng Qiu; Marcia J Kieliszewski
Journal:  J Biol Chem       Date:  2010-05-20       Impact factor: 5.157

3.  Putative fasciclin-like arabinogalactan-proteins (FLA) in wheat (Triticum aestivum) and rice (Oryza sativa): identification and bioinformatic analyses.

Authors:  Ahmed Faik; Jaouad Abouzouhair; Fathey Sarhan
Journal:  Mol Genet Genomics       Date:  2006-08-31       Impact factor: 3.291

4.  Plus and minus sexual agglutinins from Chlamydomonas reinhardtii.

Authors:  Patrick J Ferris; Sabine Waffenschmidt; James G Umen; Huawen Lin; Jae-Hyeok Lee; Koichi Ishida; Takeaki Kubo; Jeffrey Lau; Ursula W Goodenough
Journal:  Plant Cell       Date:  2005-01-19       Impact factor: 11.277

5.  Arabinogalactan proteins are required for apical cell extension in the moss Physcomitrella patens.

Authors:  Kieran J D Lee; Yoichi Sakata; Shaio-Lim Mau; Filomena Pettolino; Antony Bacic; Ralph S Quatrano; Celia D Knight; J Paul Knox
Journal:  Plant Cell       Date:  2005-09-30       Impact factor: 11.277

6.  Chlamydomonas reinhardtii has multiple prolyl 4-hydroxylases, one of which is essential for proper cell wall assembly.

Authors:  Katriina Keskiaho; Reija Hieta; Raija Sormunen; Johanna Myllyharju
Journal:  Plant Cell       Date:  2007-01-12       Impact factor: 11.277

Review 7.  Role of the extensin superfamily in primary cell wall architecture.

Authors:  Derek T A Lamport; Marcia J Kieliszewski; Yuning Chen; Maura C Cannon
Journal:  Plant Physiol       Date:  2011-03-17       Impact factor: 8.340

8.  Poplar genes encoding fasciclin-like arabinogalactan proteins are highly expressed in tension wood.

Authors:  Florian Lafarguette; Jean-Charles Leplé; Annabelle Déjardin; Françoise Laurans; Guy Costa; Marie-Claude Lesage-Descauses; Gilles Pilate
Journal:  New Phytol       Date:  2004-10       Impact factor: 10.151

9.  Between-species analysis of short-repeat modules in cell wall and sex-related hydroxyproline-rich glycoproteins of Chlamydomonas.

Authors:  Jae-Hyeok Lee; Sabine Waffenschmidt; Linda Small; Ursula Goodenough
Journal:  Plant Physiol       Date:  2007-06-15       Impact factor: 8.340

10.  Engineering of N. benthamiana L. plants for production of N-acetylgalactosamine-glycosylated proteins--towards development of a plant-based platform for production of protein therapeutics with mucin type O-glycosylation.

Authors:  Sasha M Daskalova; Josiah E Radder; Zbigniew A Cichacz; Sam H Olsen; George Tsaprailis; Hugh Mason; Linda C Lopez
Journal:  BMC Biotechnol       Date:  2010-08-24       Impact factor: 2.563

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