Abstract
Arabinogalactan-proteins (AGPs) have been purified from the plasma membrane of suspension-cultured Paul's Scarlet rose (Rosa sp.) cells. The two most abundant and homogeneous plasma membrane AGP fractions were named plasma membrane AGP1 (PM-AGP1) and plasma membrane AGP2 (PM-AGP2) and had apparent molecular masses of 140 and 217 kD, respectively. Both PM-AGP1 and PM-AGP2 had [beta]-(1-3)-, [beta]-(1,6)-, and [beta]-(1,3,6)-galactopyranosyl residues, predominantly terminal [alpha]-arabinofuranosyl residues, and (1,4)- and terminal glucuronopyranosyl residues. The protein moieties of PM-AGP1 and PM-AGP2 were both rich in hydroxyproline, alanine, and serine, but differed in the abundance of hydroxyproline, which was 1.6 times higher in PM-AGP2 than in PM-AGP1. Another difference was the overall protein content, which was 3.7% (w/w) in PM-AGP1 and 15% in PM-AGP2. As judged by their behavior on reverse-phase chromatography, PM-AGP1 and PM-AGP2 were not more hydrophobic than AGPs from the cell wall or culture medium. In contrast, a minor plasma membrane AGP fraction eluted later on reverse-phase chromatography and was more negatively charged at pH 5 than either PM-AGP1 or PM-AGP2. The more negatively charged fraction contained molecules with a glycosyl composition characteristic of AGPs and included at least two different macromolecules. The results of this investigation indicate that Rosa plasma membrane contains at least four distinct AGPs or AGP-like molecules. These molecules differed from each other in size, charge, hydrophobicity, amino-acyl composition, and/or protein content.
Full Text
The Full Text of this article is available as a PDF (1.6 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Baldwin T. C., McCann M. C., Roberts K. A Novel Hydroxyproline-Deficient Arabinogalactan Protein Secreted by Suspension-Cultured Cells of Daucus carota (Purification and Partial Characterization). Plant Physiol. 1993 Sep;103(1):115–123. doi: 10.1104/pp.103.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen C. G., Pu Z. Y., Moritz R. L., Simpson R. J., Bacic A., Clarke A. E., Mau S. L. Molecular cloning of a gene encoding an arabinogalactan-protein from pear (Pyrus communis) cell suspension culture. Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10305–10309. doi: 10.1073/pnas.91.22.10305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cheung A. Y., Wang H., Wu H. M. A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth. Cell. 1995 Aug 11;82(3):383–393. doi: 10.1016/0092-8674(95)90427-1. [DOI] [PubMed] [Google Scholar]
- De Ruiter G. A., Schols H. A., Voragen A. G., Rombouts F. M. Carbohydrate analysis of water-soluble uronic acid-containing polysaccharides with high-performance anion-exchange chromatography using methanolysis combined with TFA hydrolysis is superior to four other methods. Anal Biochem. 1992 Nov 15;207(1):176–185. doi: 10.1016/0003-2697(92)90520-h. [DOI] [PubMed] [Google Scholar]
- Du H., Simpson R. J., Clarke A. E., Bacic A. Molecular characterization of a stigma-specific gene encoding an arabinogalactan-protein (AGP) from Nicotiana alata. Plant J. 1996 Mar;9(3):313–323. doi: 10.1046/j.1365-313x.1996.09030313.x. [DOI] [PubMed] [Google Scholar]
- Du H., Simpson R. J., Moritz R. L., Clarke A. E., Bacic A. Isolation of the protein backbone of an arabinogalactan-protein from the styles of Nicotiana alata and characterization of a corresponding cDNA. Plant Cell. 1994 Nov;6(11):1643–1653. doi: 10.1105/tpc.6.11.1643. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gane A. M., Craik D., Munro S. L., Howlett G. J., Clarke A. E., Bacic A. Structural analysis of the carbohydrate moiety of arabinogalactan-proteins from stigmas and styles of Nicotiana alata. Carbohydr Res. 1995 Nov 7;277(1):67–85. doi: 10.1016/0008-6215(95)00197-2. [DOI] [PubMed] [Google Scholar]
- Gell A. C., Bacic A., Clarke A. E. Arabinogalactan-Proteins of the Female Sexual Tissue of Nicotiana alata: I. Changes during Flower Development and Pollination. Plant Physiol. 1986 Dec;82(4):885–889. doi: 10.1104/pp.82.4.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gleeson P. A., Clarke A. E. Structural studies on the major component of Gladiolus style mucilage, an arabinogalactan-protein. Biochem J. 1979 Sep 1;181(3):607–621. doi: 10.1042/bj1810607. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gleeson P. A., McNamara M., Wettenhall R. E., Stone B. A., Fincher G. B. Characterization of the hydroxyproline-rich protein core of an arabinogalactan-protein secreted from suspension-cultured Lolium multiflorum (Italian ryegrass) endosperm cells. Biochem J. 1989 Dec 15;264(3):857–862. doi: 10.1042/bj2640857. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Herman E. M., Lamb C. J. Arabinogalactan-rich glycoproteins are localized on the cell surface and in intravacuolar multivesicular bodies. Plant Physiol. 1992 Jan;98(1):264–272. doi: 10.1104/pp.98.1.264. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kieliszewski M. J., Kamyab A., Leykam J. F., Lamport D. T. A Histidine-Rich Extensin from Zea mays Is an Arabinogalactan Protein. Plant Physiol. 1992 Jun;99(2):538–547. doi: 10.1104/pp.99.2.538. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kikuchi S., Ohinata A., Tsumuraya Y., Hashimoto Y., Kaneko Y., Matsushima H. Production and characterization of antibodies to the beta-(1-->6)-galactotetraosyl group and their interaction with arabinogalactan-proteins. Planta. 1993;190(4):525–535. doi: 10.1007/BF00224792. [DOI] [PubMed] [Google Scholar]
- Komalavilas P., Zhu J. K., Nothnagel E. A. Arabinogalactan-proteins from the suspension culture medium and plasma membrane of rose cells. J Biol Chem. 1991 Aug 25;266(24):15956–15965. [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Mau S. L., Chen C. G., Pu Z. Y., Moritz R. L., Simpson R. J., Bacic A., Clarke A. E. Molecular cloning of cDNAs encoding the protein backbones of arabinogalactan-proteins from the filtrate of suspension-cultured cells of Pyrus communis and Nicotiana alata. Plant J. 1995 Aug;8(2):269–281. doi: 10.1046/j.1365-313x.1995.08020269.x. [DOI] [PubMed] [Google Scholar]
- Nothnagel E. A., Lyon J. L. Structural requirements for the binding of phenylglycosides to the surface of protoplasts. Plant Physiol. 1986 Jan;80(1):91–98. doi: 10.1104/pp.80.1.91. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pennell R. I., Janniche L., Kjellbom P., Scofield G. N., Peart J. M., Roberts K. Developmental Regulation of a Plasma Membrane Arabinogalactan Protein Epitope in Oilseed Rape Flowers. Plant Cell. 1991 Dec;3(12):1317–1326. doi: 10.1105/tpc.3.12.1317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pennell R. I., Janniche L., Scofield G. N., Booij H., de Vries S. C., Roberts K. Identification of a transitional cell state in the developmental pathway to carrot somatic embryogenesis. J Cell Biol. 1992 Dec;119(5):1371–1380. doi: 10.1083/jcb.119.5.1371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pennell R. I., Knox J. P., Scofield G. N., Selvendran R. R., Roberts K. A family of abundant plasma membrane-associated glycoproteins related to the arabinogalactan proteins is unique to flowering plants. J Cell Biol. 1989 May;108(5):1967–1977. doi: 10.1083/jcb.108.5.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qi W., Fong C., Lamport D. T. Gum arabic glycoprotein is a twisted hairy rope : a new model based on o-galactosylhydroxyproline as the polysaccharide attachment site. Plant Physiol. 1991 Jul;96(3):848–855. doi: 10.1104/pp.96.3.848. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saulnier L., Brillouet J. M., Moutounet M., Hervé du Penhoat C., Michon V. New investigations of the structure of grape arabinogalactan-protein. Carbohydr Res. 1992 Feb 7;224:219–235. doi: 10.1016/0008-6215(92)84108-5. [DOI] [PubMed] [Google Scholar]
- Serpe M. D., Nothnagel E. A. Fractionation and Structural Characterization of Arabinogalactan-Proteins from the Cell Wall of Rose Cells. Plant Physiol. 1995 Nov;109(3):1007–1016. doi: 10.1104/pp.109.3.1007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsai C. M., Frasch C. E. A sensitive silver stain for detecting lipopolysaccharides in polyacrylamide gels. Anal Biochem. 1982 Jan 1;119(1):115–119. doi: 10.1016/0003-2697(82)90673-x. [DOI] [PubMed] [Google Scholar]
- Yanagishita M., Hascall V. C. Cell surface heparan sulfate proteoglycans. J Biol Chem. 1992 May 15;267(14):9451–9454. [PubMed] [Google Scholar]