Registro:

Referencias:

• Breton, C., Heissigerova, H., Jeanneau, C., Moravcova, J., Imberty, A., Comparative aspects of glycosyltransferases (2002) Biochem Soc Symp, pp. 23-32
• Coutinho, P.M., Stam, M., Blanc, E., Henrissat, B., Why are there so many carbohydrate-active enzyme-related genes in plants (2003) Trends in Plant Science, 8, pp. 563-565
• Ellis, M., Egelund, J., Schultz, C.J., Bacic, A., Arabinogalactan-proteins: Key regulators at the cell surface (2010) Plant Physiol, 153, pp. 403-419
• Lamport, D.T., Kieliszewski, M.J., Chen, Y., Cannon, M.C., Role of the extensin superfamily in primary cell wall architecture (2011) Plant Physiol, 156, pp. 11-19
• Lamport, D.T., Miller, D.H., Hydroxyproline arabinosides in the plant kingdom (1971) Plant Physiol, 48, pp. 454-456
• Tan, L., Leykam, J.F., Kieliszewski, M.J., Glycosylation motifs that direct arabinogalactan addition to arabinogalactan-proteins (2003) Plant Physiology, 132, pp. 1362-1369
• Xu, J., Tan, L., Lamport, D.T., Showalter, A.M., Kieliszewski, M.J., The O-Hyp glycosylation code in tobacco and Arabidopsis and a proposed role of Hyp-glycans in secretion (2008) Phytochemistry, 69, pp. 1631-1640
• Chakraborty, S., YeATS-A tool suite for analyzing RNA-seq derived transcriptome identifies a highly transcribed putative extensin in heartwood/sapwood transition zone in black walnut (2015) F1000 Res, 4, p. 155
• Bollig, K., Structural analysis of linear hydroxyproline-bound O-glycans of Chlamydomonas reinhardtii-conservation of the inner core in Chlamydomonas and land plants (2007) Carbohydr Res, 342, pp. 2557-2566
• Miller, D.H., Lamport, D.T., Miller, M., Hydroxyproline heterooligosaccharides in Chlamydomonas (1972) Science, 176, pp. 918-920
• Akiyama, Y., Mori, M., Kat, K., 13C-NMR Analysis of Hydroxy-proline Arabinosides from Nicotiana tabacum (1980) Agricultural and Biological Chemistry, 44, pp. 2487-2489
• Campargue, C., Lafitte, C., Esquerre-Tugaye, M.T., Mazau, D., Analysis of hydroxyproline and hydroxyproline-arabinosides of plant origin by high-performance anion-exchange chromatography-pulsed amperometric detection (1998) Anal Biochem, 257, pp. 20-25
• Lamport, D.T.A., Katona, L., Roerig, S., Galactosylserine in extensin (1973) Biochemical Journal, 133, pp. 125-132
• Matsubayashi, Y., Post-translational modifications in secreted peptide hormones in plants (2011) Plant Cell Physiol, 52, pp. 5-13
• Kohorn, B.D., Kohorn, S.L., The cell wall-associated kinases, WAKs, as pectin receptors (2012) Front Plant Sci, 3, p. 88
• Nakhamchik, A., A comprehensive expression analysis of the Arabidopsis proline-rich extensin-like receptor kinase gene family using bioinformatic and experimental approaches (2004) Plant Cell Physiol, 45, pp. 1875-1881
• Halim, A., Glycoproteomic analysis of seven major allergenic proteins reveals novel post-translational modifications (2015) Molecular & Cellular Proteomics, 14, pp. 191-204
• Saito, F., Identification of Novel Peptidyl Serine alpha-Galactosyltransferase Gene Family in Plants (2014) The Journal of Biological Chemistry, 289, pp. 20405-20420
• Showalter, A.M., Keppler, B., Lichtenberg, J., Gu, D., Welch, L.R., A bioinformatics approach to the identification, classification, and analysis of hydroxyproline-rich glycoproteins (2010) Plant Physiol, 153, pp. 485-513
• Velasquez, S.M., O-glycosylated cell wall proteins are essential in root hair growth (2011) Science, 332, pp. 1401-1403
• Velasquez, S.M., Complex regulation of prolyl-4-hydroxylases impacts root hair expansion (2015) Mol Plant, 8, pp. 734-746
• Ogawa-Ohnishi, M., Matsushita, W., Matsubayashi, Y., Identification of three hydroxyproline O-arabinosyltransferases in Arabidopsis thaliana (2013) Nat Chem Biol, 9, pp. 726-730
• Egelund, J., Molecular characterization of two Arabidopsis thaliana glycosyltransferase mutants, rra1 and rra2, which have a reduced residual arabinose content in a polymer tightly associated with the cellulosic wall residue (2007) Plant Mol Biol, 64, pp. 439-451
• Gille, S., Hansel, U., Ziemann, M., Pauly, M., Identification of plant cell wall mutants by means of a forward chemical genetic approach using hydrolases (2009) Proc Natl Acad Sci USA, 106, pp. 14699-14704
• Yang, Z., Toward stable genetic engineering of human o-glycosylation in plants (2012) Plant Physiology, 160, pp. 450-463
• Schoberer, J., Arginine/lysine residues in the cytoplasmic tail promote ER export of plant glycosylation enzymes (2009) Traffic, 10, pp. 101-115
• Strasser, R., Molecular cloning and characterization of Arabidopsis thaliana Golgi-mannosidase II, a key enzyme in the formation of complex N-glycans in plants (2006) The Plant Journal, 45, pp. 789-803
• Boevink, P., Stacks on tracks: The plant Golgi apparatus traffics on an actin/ER network (1998) Plant J, 15, pp. 441-447
• Ma, B., Simala-Grant, J.L., Taylor, D.E., Fucosylation in prokaryotes and eukaryotes (2006) Glycobiology, 16, pp. 158R-184R
• Hayashida, M., Fujii, T., Hamasu, M., Ishiguro, M., Hata, Y., Similarity between protein-protein and protein-carbohydrate interactions, revealed by two crystal structures of lectins from the roots of pokeweed (2003) J Mol Biol, 334, pp. 551-565
• Mihara, M., Itoh, T., Izawa, T., SALAD database: A motif-based database of protein annotations for plant comparative genomics (2010) Nucleic Acids Research, 38, pp. D835-D842
• Hori, K., Klebsormidium flaccidum genome reveals primary factors for plant terrestrial adaptation (2014) Nat Commun, 5, p. 3978
• Liu, X., Bioinformatic identification and analysis of extensins in the plant kingdom (2016) PLoS One, 11, p. e0150177
• MacAlister, C.A., Ortiz-Ramirez, C., Becker, J.D., Feijo, J.A., Lippman, Z.B., Hydroxyproline O-arabinosyltransferase mutants oppositely alter tip growth in Arabidopsis thaliana and Physcomitrella patens (2016) Plant J, 85, pp. 193-208
• Ulvskov, P., Paiva, D.S., Domozych, D., Harholt, J., Classification, naming and evolutionary history of glycosyltransferases from sequenced green and red algal genomes (2013) PLoS One, 8, p. e76511
• Christiansen, C., The carbohydrate-binding module family 20-diversity, structure, and function (2009) FEBS J, 276, pp. 5006-5029
• Alderwick, L.J., The C-terminal domain of the Arabinosyltransferase Mycobacterium tuberculosis EmbC is a lectin-like carbohydrate binding module (2011) PLoS Pathog, 7, p. e1001299
• Basu, D., Functional identification of a hydroxyproline-o-galactosyltransferase specific for arabinogalactan protein biosynthesis in Arabidopsis (2013) J Biol Chem, 288, pp. 10132-10143
• Gazave, E., Origin and evolution of the Notch signalling pathway: An overview from eukaryotic genomes (2009) BMC Evol Biol, 9, p. 249
• Acar, M., Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling (2008) Cell, 132, pp. 247-258
• Sorensen, I., The charophycean green algae provide insights into the early origins of plant cell walls (2011) Plant J, 68, pp. 201-211
• Domozych, S., Wells, D.B., Shaw, J.P., Basket scales of the green alga, mesostigma viride: Chemistry and ultrastructure (1991) Journal of Cell Science, 100, p. 397
• Harholt, J., The glycosyltransferase repertoire of the spikemoss Selaginella moellendorffii and a comparative study of its cell wall (2012) Plos One, 7, p. e35846
• Wickett, N.J., Phylotranscriptomic analysis of the origin and early diversification of land plants (2014) Proc Natl Acad Sci USA, 111, pp. E4859-4868
• Matasci, N., Data access for the 1, 000 Plants (1KP) project (2014) Gigascience, 3, p. 17
• Xie, Y., SOAPdenovo-Trans: De novo transcriptome assembly with short RNA-Seq reads (2014) Bioinformatics, 30, pp. 1660-1666
• Johnson, M.T., Evaluating methods for isolating total RNA and predicting the success of sequencing phylogenetically diverse plant transcriptomes (2012) PLoS One, 7, p. e50226
• Edgar, R.C., MUSCLE: Multiple sequence alignment with high accuracy and high throughput (2004) Nucleic Acids Res, 32, pp. 1792-1797
• Mitchell, A., The InterPro protein families database: The classification resource after 15 years (2015) Nucleic Acids Res, 43, pp. D213-221
• Kall, L., Krogh, A., Sonnhammer, E.L., A combined transmembrane topology and signal peptide prediction method (2004) J Mol Biol, 338, pp. 1027-1036
• Brady, S.M., A high-resolution root spatiotemporal map reveals dominant expression patterns (2007) Science, 318, pp. 801-806
• Ciucanu, I., Kerek, F., A simple and rapid method for the permethylation of carbohydrates (1984) Carbohydrate Research, 131, pp. 209-217. , http://dx.doi.org/10.1016/0008-6215(84)85242-8
• Ciucanu, I., Per-O-methylation reaction for structural analysis of carbohydrates by mass spectrometry (2006) Anal Chim Acta, 576, pp. 147-155
• Kivirikko, K.I., Liesmaa, M., A colorimetric method for determination of hydroxyproline in tissue hydrolysates (1959) Scand. J. Clin. Lab. Invest., 11, pp. 128-133
• Schoberer, J., Sequential depletion and acquisition of proteins during Golgi stack disassembly and reformation (2010) Traffic, 11, pp. 1429-1444
• Knoch, E., A beta-glucuronosyltransferase from Arabidopsis thaliana involved in biosynthesis of type II arabinogalactan has a role in cell elongation during seedling growth (2013) Plant J, 76, pp. 1016-1029
• Earley, K.W., Gateway-compatible vectors for plant functional genomics and proteomics (2006) Plant J, 45, pp. 616-629
• Markwardt, M.L., An improved cerulean fluorescent protein with enhanced brightness and reduced reversible photoswitching (2011) Plos One, 6, p. e17896
• Abdulrazzak, N., A coumaroyl-ester-3-hydroxylase insertion mutant reveals the existence of nonredundant meta-hydroxylation pathways and essential roles for phenolic precursors in cell expansion and plant growth (2006) Plant Physiol, 140, pp. 30-48
• Byg, I., Large-scale extraction of rhamnogalacturonan i from industrial potato waste (2012) Food Chemistry, 131, pp. 1207-1216. , http://dx.doi.org/10.1016/j.foodchem.2011.09.106
• Madson, M., The MUR3 gene of Arabidopsis encodes a xyloglucan galactosyltransferase that is evolutionarily related to animal exostosins (2003) Plant Cell, 15, pp. 1662-1670
• Harholt, J., Arabinan Deficient 1 is a Putative Arabinosyltransferase Involved in Biosynthesis of Pectic Arabinan in Arabidopsis (2006) Plant Physiology, 140, pp. 49-58
• Jensen, J.K., Identification of a xylogalacturonan xylosyltransferase involved in pectin biosynthesis in Arabidopsis (2008) Plant Cell, 20, pp. 1289-1302
• Brown, D.M., Zhang, Z., Stephens, E., Dupree, P., Turner, S.R., Characterization of IRX10 and IRX10-like reveals an essential role in glucuronoxylan biosynthesis in Arabidopsis (2009) Plant J, 57, pp. 732-746
• Zhong, R., Arabidopsis fragile fiber8, which encodes a putative glucuronyltransferase, is essential for normal secondary wall synthesis (2005) Plant Cell, 17, pp. 3390-3408
• Winter, D., An "Electronic Fluorescent Pictograph" browser for exploring and analyzing large-scale biological data sets (2007) PLoS One, 2, p. e718
• Lind, T., Tufaro, F., McCormick, C., Lindahl, U., Lidholt, K., The putative tumor suppressors EXT1 and EXT2 are glycosyltransferases required for the biosynthesis of heparan sulfate (1998) The Journal of Biological Chemistry, 273, pp. 26265-26268

Citas:

---------- APA ----------

---------- CHICAGO ----------

---------- MLA ----------

---------- VANCOUVER ----------