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dc.contributor.author | Corral Martínez, Patricia | es_ES |
dc.contributor.author | García-Fortea, Edgar | es_ES |
dc.contributor.author | Bernard, Sophie | es_ES |
dc.contributor.author | Driouich, Azeddine | es_ES |
dc.contributor.author | Seguí-Simarro, Jose M. | es_ES |
dc.date.accessioned | 2018-02-06T08:19:55Z | |
dc.date.available | 2018-02-06T08:19:55Z | |
dc.date.issued | 2016 | es_ES |
dc.identifier.issn | 0032-0781 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/96982 | |
dc.description.abstract | [EN] In this work, we performed an extensive and detailed analysis of the changes in cell wall composition during Brassica napus anther development. We used immunogold labeling to study the spatial and temporal patterns of composition and distribution of different AGP, pectin, xyloglucan and xylan epitopes in high pressure-frozen/freeze-substituted anthers, quantifying and comparing their relative levels in the different anther tissues and developmental stages. We used the following monoclonal antibodies: JIM13, JIM8, JIM14 and JIM16 for AGPs, LM5, LM6, JIM7, JIM5 and LM7 for pectins, CCRC-M1, CCRC-M89 and LM15 for xyloglucan, and LM11 for xylan. Each cell wall epitope showed a characteristic temporal and spatial labeling pattern. Microspore, pollen and tapetal cells showed similar patterns for each epitope, whereas the outermost anther layers (epidermis, endothecium and middle layers) presented remarkably different patterns. Our results suggested that AGPs, pectins, xyloglucan and xylan have specific roles during anther development. The AGP epitopes studied appeared to belong to AGPs specifically involved in microspore differentiation, and contributed first by the tapetum and then, upon tapetal dismantling, by the endothecium and middle layers. In contrast, the changes in pectin and hemicellulose epitopes suggested a specific role in anther dehiscence, facilitating anther wall weakening and rupture. The distribution of the different cell wall constituents is regulated in a tissue and stage-specific manner, which seems directly related with the role of each tissue at each stage. | es_ES |
dc.description.sponsorship | This work was supported by the Spanish Ministry of Economy (MINECO) jointly funded by le Fonds europeen de developpement regional (FEDER) [grants AGL2010-17895, AGL2014-55177 to J.M.S.S.]; La Region de Haute Normandie and le Grand Reseau de Recherche-Vegetal, Agronomie, Sol et Innovation, l'Universite de Rouen [financial support to A.D.]; FEDER [financial support to A.D.]; l'Agence nationale de la recherche (ANR) [financial support to A.D.]. | en_EN |
dc.language | Inglés | es_ES |
dc.publisher | Oxford University Press | es_ES |
dc.relation.ispartof | Plant and Cell Physiology | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | AGPs | es_ES |
dc.subject | Cell wall | es_ES |
dc.subject | Microspore | es_ES |
dc.subject | Pollen | es_ES |
dc.subject | Xylan | es_ES |
dc.subject | Xyloglucan | es_ES |
dc.subject | Electron Microscopy Service of the UPV | |
dc.subject.classification | GENETICA | es_ES |
dc.title | Ultrastructural immunolocalization of arabinogalactan protein, pectin and hemicellulose epitopes through anther development in Brassica napus | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1093/pcp/pcw133 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//AGL2014-55177-R/ES/NUEVAS VIAS DE MEJORA DE LA EMBRIOGENESIS DE MICROSPORAS EN SOLANACEAS RECALCITRANTES: ESTUDIO DE LA AUTOFAGIA, LA UPR Y LA REGULACION HORMONAL/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//AGL2010-17895/ES/GENERACION EFICIENTE DE DOBLE HAPLOIDES EN BERENJENA Y PIMIENTO MEDIANTE CULTIVO IN VITRO DE MICROSPORAS AISLADAS. ANALISIS CELULAR Y MOLECULAR DEL DESARROLLO ANDROGENICO/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario de Conservación y Mejora de la Agrodiversidad Valenciana - Institut Universitari de Conservació i Millora de l'Agrodiversitat Valenciana | es_ES |
dc.description.bibliographicCitation | Corral Martínez, P.; García-Fortea, E.; Bernard, S.; Driouich, A.; Seguí-Simarro, JM. (2016). Ultrastructural immunolocalization of arabinogalactan protein, pectin and hemicellulose epitopes through anther development in Brassica napus. Plant and Cell Physiology. 57(10):2161-2174. https://doi.org/10.1093/pcp/pcw133 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | http://doi.org/10.1093/pcp/pcw133 | es_ES |
dc.description.upvformatpinicio | 2161 | es_ES |
dc.description.upvformatpfin | 2174 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 57 | es_ES |
dc.description.issue | 10 | es_ES |
dc.identifier.pmid | 27481894 | |
dc.relation.pasarela | S\318748 | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |
dc.description.references | Antoine, A. F., Faure, J.-E., Cordeiro, S., Dumas, C., Rougier, M., & Feijo, J. A. (2000). A calcium influx is triggered and propagates in the zygote as a wavefront during in vitro fertilization of flowering plants. Proceedings of the National Academy of Sciences, 97(19), 10643-10648. doi:10.1073/pnas.180243697 | es_ES |
dc.description.references | Aouali, N., Laporte, P., & Clément, C. (2001). Pectin secretion and distribution in the anther during pollen development in Lilium. Planta, 213(1), 71-79. doi:10.1007/s004250000469 | es_ES |
dc.description.references | Atmodjo, M. A., Hao, Z., & Mohnen, D. (2013). Evolving Views of Pectin Biosynthesis. Annual Review of Plant Biology, 64(1), 747-779. doi:10.1146/annurev-arplant-042811-105534 | es_ES |
dc.description.references | Barany, I., Fadon, B., Risueno, M. C., & Testillano, P. S. (2010). Cell wall components and pectin esterification levels as markers of proliferation and differentiation events during pollen development and pollen embryogenesis in Capsicum annuum L. Journal of Experimental Botany, 61(4), 1159-1175. doi:10.1093/jxb/erp392 | es_ES |
dc.description.references | Bouton, S., Leboeuf, E., Mouille, G., Leydecker, M.-T., Talbotec, J., Granier, F., … Truong, H.-N. (2002). QUASIMODO1 Encodes a Putative Membrane-Bound Glycosyltransferase Required for Normal Pectin Synthesis and Cell Adhesion in Arabidopsis. The Plant Cell, 14(10), 2577-2590. doi:10.1105/tpc.004259 | es_ES |
dc.description.references | Carpita, N., & Gibeaut, D. (1993). Structural models of primary cell walls in flowering plants: consistency of molecular structure with the physical properties of the walls during growth. The Plant Journal, 3(1), 1-30. doi:10.1046/j.1365-313x.1993.00999.x | es_ES |
dc.description.references | Coimbra, S., Almeida, J., Junqueira, V., Costa, M. L., & Pereira, L. G. (2007). Arabinogalactan proteins as molecular markers in Arabidopsis thaliana sexual reproduction. Journal of Experimental Botany, 58(15-16), 4027-4035. doi:10.1093/jxb/erm259 | es_ES |
dc.description.references | Corral-Martínez, P., & Seguí-Simarro, J. M. (2013). Refining the method for eggplant microspore culture: effect of abscisic acid, epibrassinolide, polyethylene glycol, naphthaleneacetic acid, 6-benzylaminopurine and arabinogalactan proteins. Euphytica, 195(3), 369-382. doi:10.1007/s10681-013-1001-4 | es_ES |
dc.description.references | Cosgrove, D. J. (1997). ASSEMBLY AND ENLARGEMENT OF THE PRIMARY CELL WALL IN PLANTS. Annual Review of Cell and Developmental Biology, 13(1), 171-201. doi:10.1146/annurev.cellbio.13.1.171 | es_ES |
dc.description.references | Cosgrove, D. J. (2005). Growth of the plant cell wall. Nature Reviews Molecular Cell Biology, 6(11), 850-861. doi:10.1038/nrm1746 | es_ES |
dc.description.references | Costa, M. L., Sobral, R., Costa, M. M. R., Amorim, M. I., & Coimbra, S. (2014). Evaluation of the presence of arabinogalactan proteins and pectins during Quercus suber male gametogenesis. Annals of Botany, 115(1), 81-92. doi:10.1093/aob/mcu223 | es_ES |
dc.description.references | Drakakaki, G. (2015). Polysaccharide deposition during cytokinesis: Challenges and future perspectives. Plant Science, 236, 177-184. doi:10.1016/j.plantsci.2015.03.018 | es_ES |
dc.description.references | Durand, C., Vicré-Gibouin, M., Follet-Gueye, M. L., Duponchel, L., Moreau, M., Lerouge, P., & Driouich, A. (2009). The Organization Pattern of Root Border-Like Cells of Arabidopsis Is Dependent on Cell Wall Homogalacturonan. Plant Physiology, 150(3), 1411-1421. doi:10.1104/pp.109.136382 | es_ES |
dc.description.references | El-Tantawy, A.-A., Solís, M.-T., Da Costa, M. L., Coimbra, S., Risueño, M.-C., & Testillano, P. S. (2013). Arabinogalactan protein profiles and distribution patterns during microspore embryogenesis and pollen development in Brassica napus. Plant Reproduction, 26(3), 231-243. doi:10.1007/s00497-013-0217-8 | es_ES |
dc.description.references | Freshour, G., Clay, R. P., Fuller, M. S., Albersheim, P., Darvill, A. G., & Hahn, M. G. (1996). Developmental and Tissue-Specific Structural Alterations of the Cell-Wall Polysaccharides of Arabidopsis thaliana Roots. Plant Physiology, 110(4), 1413-1429. doi:10.1104/pp.110.4.1413 | es_ES |
dc.description.references | Gomez, L. D., Steele-King, C. G., Jones, L., Foster, J. M., Vuttipongchaikij, S., & McQueen-Mason, S. J. (2009). Arabinan Metabolism during Seed Development and Germination in Arabidopsis. Molecular Plant, 2(5), 966-976. doi:10.1093/mp/ssp050 | es_ES |
dc.description.references | Hao, Z., Avci, U., Tan, L., Zhu, X., Glushka, J., Pattathil, S., … Mohnen, D. (2014). Loss of Arabidopsis GAUT12/IRX8 causes anther indehiscence and leads to reduced G lignin associated with altered matrix polysaccharide deposition. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00357 | es_ES |
dc.description.references | Harholt, J., Suttangkakul, A., & Vibe Scheller, H. (2010). Biosynthesis of Pectin. Plant Physiology, 153(2), 384-395. doi:10.1104/pp.110.156588 | es_ES |
dc.description.references | Hervé, C., Rogowski, A., Gilbert, H. J., & Paul Knox, J. (2009). Enzymatic treatments reveal differential capacities for xylan recognition and degradation in primary and secondary plant cell walls. The Plant Journal, 58(3), 413-422. doi:10.1111/j.1365-313x.2009.03785.x | es_ES |
dc.description.references | Jones, L., Seymour, G. B., & Knox, J. P. (1997). Localization of Pectic Galactan in Tomato Cell Walls Using a Monoclonal Antibody Specific to (1[->]4)-[beta]-D-Galactan. Plant Physiology, 113(4), 1405-1412. doi:10.1104/pp.113.4.1405 | es_ES |
dc.description.references | Kikuchi, A., Satoh, S., Nakamura, N., & Fujii, T. (1995). Differences in pectic polysaccharides between carrot embryogenic and non-embryogenic calli. Plant Cell Reports, 14(5). doi:10.1007/bf00232028 | es_ES |
dc.description.references | Knox, J. P., Linstead, P., King, J., Cooper, C., & Roberts, K. (1990). Pectin esterification is spatially regulated both within cell walls and between developing tissues of root apices. Planta, 181(4). doi:10.1007/bf00193004 | es_ES |
dc.description.references | Knox, J. ., Linstead, P. ., Cooper, J. P. C., & Roberts, K. (1991). Developmentally regulated epitopes of cell surface arabinogalactan proteins and their relation to root tissue pattern formation. The Plant Journal, 1(3), 317-326. doi:10.1046/j.1365-313x.1991.t01-9-00999.x | es_ES |
dc.description.references | Lamport, D. T. A., & Várnai, P. (2012). Periplasmic arabinogalactan glycoproteins act as a calcium capacitor that regulates plant growth and development. New Phytologist, 197(1), 58-64. doi:10.1111/nph.12005 | es_ES |
dc.description.references | Lopez, R. A., & Renzaglia, K. S. (2014). Multiflagellated sperm cells ofCeratopteris richardiiare bathed in arabinogalactan proteins throughout development. American Journal of Botany, 101(12), 2052-2061. doi:10.3732/ajb.1400424 | es_ES |
dc.description.references | Lopez, R. A., & Renzaglia, K. S. (2016). Arabinogalactan proteins and arabinan pectins abound in the specialized matrices surrounding female gametes of the fern Ceratopteris richardii. Planta, 243(4), 947-957. doi:10.1007/s00425-015-2448-4 | es_ES |
dc.description.references | Majewska-Sawka, A., & M�nster, A. (2003). Cell-wall antigens in mesophyll cells and mesophyll-derived protoplasts of sugar beet: possible implication in protoplast recalcitrance? Plant Cell Reports, 21(10), 946-954. doi:10.1007/s00299-003-0612-y | es_ES |
dc.description.references | Majewska-Sawka, A., Münster, A., & Wisniewska, E. (2004). Temporal and Spatial Distribution of Pectin Epitopes in Differentiating Anthers and Microspores of Fertile and Sterile Sugar Beet. Plant and Cell Physiology, 45(5), 560-572. doi:10.1093/pcp/pch066 | es_ES |
dc.description.references | Marcus, S. E., Verhertbruggen, Y., Hervé, C., Ordaz-Ortiz, J. J., Farkas, V., Pedersen, H. L., … Knox, J. P. (2008). Pectic homogalacturonan masks abundant sets of xyloglucan epitopes in plant cell walls. BMC Plant Biology, 8(1), 60. doi:10.1186/1471-2229-8-60 | es_ES |
dc.description.references | McCartney, L., Marcus, S. E., & Knox, J. P. (2005). Monoclonal Antibodies to Plant Cell Wall Xylans and Arabinoxylans. Journal of Histochemistry & Cytochemistry, 53(4), 543-546. doi:10.1369/jhc.4b6578.2005 | es_ES |
dc.description.references | McCartney, L., Ormerod, andrew P., Gidley, M. J., & Knox, J. P. (2000). Temporal and spatial regulation of pectic (14)-beta-D-galactan in cell walls of developing pea cotyledons: implications for mechanical properties. The Plant Journal, 22(2), 105-113. doi:10.1046/j.1365-313x.2000.00719.x | es_ES |
dc.description.references | McCartney, L., Steele-King, C. G., Jordan, E., & Knox, J. P. (2003). Cell wall pectic (1→4)-β-d-galactan marks the acceleration of cell elongation in theArabidopsisseedling root meristem. The Plant Journal, 33(3), 447-454. doi:10.1046/j.1365-313x.2003.01640.x | es_ES |
dc.description.references | Moore, J. P., Nguema-Ona, E. E., Vicré-Gibouin, M., Sørensen, I., Willats, W. G. T., Driouich, A., & Farrant, J. M. (2012). Arabinose-rich polymers as an evolutionary strategy to plasticize resurrection plant cell walls against desiccation. Planta, 237(3), 739-754. doi:10.1007/s00425-012-1785-9 | es_ES |
dc.description.references | Mortimer, J. C., Faria-Blanc, N., Yu, X., Tryfona, T., Sorieul, M., Ng, Y. Z., … Dupree, P. (2015). An unusual xylan in Arabidopsis primary cell walls is synthesised by GUX3, IRX9L, IRX10L and IRX14. The Plant Journal, 83(3), 413-426. doi:10.1111/tpj.12898 | es_ES |
dc.description.references | Otegui, M. S., Capp, R., & Staehelin, L. A. (2002). Developing Seeds of Arabidopsis Store Different Minerals in Two Types of Vacuoles and in the Endoplasmic Reticulum. The Plant Cell, 14(6), 1311-1327. doi:10.1105/tpc.010486 | es_ES |
dc.description.references | Otegui, M. S., & Staehelin, L. A. (2004). Electron tomographic analysis of post-meiotic cytokinesis during pollen development in Arabidopsis thaliana. Planta, 218(4), 501-515. doi:10.1007/s00425-003-1125-1 | es_ES |
dc.description.references | Owen, H. A., & Makaroff, C. A. (1995). Ultrastructure of microsporogenesis and microgametogenesis inArabidopsis thaliana (L.) Heynh. ecotype Wassilewskija (Brassicaceae). Protoplasma, 185(1-2), 7-21. doi:10.1007/bf01272749 | es_ES |
dc.description.references | Paire, A., Devaux, P., Lafitte, C., Dumas, C., & Matthys-Rochon, E. (2003). Plant Cell, Tissue and Organ Culture, 73(2), 167-176. doi:10.1023/a:1022805623167 | es_ES |
dc.description.references | Parra-Vega, V., Corral-Martínez, P., Rivas-Sendra, A., & Seguí-Simarro, J. M. (2015). Induction of Embryogenesis in Brassica Napus Microspores Produces a Callosic Subintinal Layer and Abnormal Cell Walls with Altered Levels of Callose and Cellulose. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.01018 | es_ES |
dc.description.references | Pattathil, S., Avci, U., Baldwin, D., Swennes, A. G., McGill, J. A., Popper, Z., … Hahn, M. G. (2010). A Comprehensive Toolkit of Plant Cell Wall Glycan-Directed Monoclonal Antibodies. Plant Physiology, 153(2), 514-525. doi:10.1104/pp.109.151985 | es_ES |
dc.description.references | Pauly, M., Qin, Q., Greene, H., Albersheim, P., Darvill, A., & York, W. S. (2001). Changes in the structure of xyloglucan during cell elongation. Planta, 212(5-6), 842-850. doi:10.1007/s004250000448 | es_ES |
dc.description.references | PENG, Y.-B., ZOU, C., GONG, H.-Q., BAI, S.-N., XU, Z.-H., & LI, Y.-Q. (2005). Immunolocalization of Arabinogalactan Proteins and Pectins in Floral Buds of Cucumber (Cucumis sativus L.) During Sex Determination. Journal of Integrative Plant Biology, 47(2), 194-200. doi:10.1111/j.1744-7909.2005.00023.x | es_ES |
dc.description.references | Pennell, R. I., Janniche, L., Kjellbom, P., Scofield, G. N., Peart, J. M., & Roberts, K. (1991). Developmental Regulation of a Plasma Membrane Arabinogalactan Protein Epitope in Oilseed Rape Flowers. The Plant Cell, 1317-1326. doi:10.1105/tpc.3.12.1317 | es_ES |
dc.description.references | Peña, M. J., Ryden, P., Madson, M., Smith, A. C., & Carpita, N. C. (2004). The Galactose Residues of Xyloglucan Are Essential to Maintain Mechanical Strength of the Primary Cell Walls in Arabidopsis during Growth. Plant Physiology, 134(1), 443-451. doi:10.1104/pp.103.027508 | es_ES |
dc.description.references | Pereira, A. M., Pereira, L. G., & Coimbra, S. (2015). Arabinogalactan proteins: rising attention from plant biologists. Plant Reproduction, 28(1), 1-15. doi:10.1007/s00497-015-0254-6 | es_ES |
dc.description.references | Roy, S., Jauh, G. Y., Hepler, P. K., & Lord, E. M. (1998). Effects of Yariv phenylglycoside on cell wall assembly in the lily pollen tube. Planta, 204(4), 450-458. doi:10.1007/s004250050279 | es_ES |
dc.description.references | Seguí-Simarro J.M. (2015) High pressure freezing and freeze substitution of in vivo and in vitro cultured plant samples. In Plant Microtechniques: Methods and Protocols. Edited by Yeung E.C.T. Stasolla C. Sumner M.J. Huang B.Q. pp. 117–134. Springer International Publishing, Switzerland. | es_ES |
dc.description.references | Seifert, G. J., & Roberts, K. (2007). The Biology of Arabinogalactan Proteins. Annual Review of Plant Biology, 58(1), 137-161. doi:10.1146/annurev.arplant.58.032806.103801 | es_ES |
dc.description.references | Shibaya, T., & Sugawara, Y. (2009). Induction of multinucleation by β-glucosyl Yariv reagent in regenerated cells from Marchantia polymorpha protoplasts and involvement of arabinogalactan proteins in cell plate formation. Planta, 230(3), 581-588. doi:10.1007/s00425-009-0954-y | es_ES |
dc.description.references | Southworth, D., & Kwiatkowski, S. (1996). Arabinogalactan proteins at the cell surface ofBrassica sperm andLilium sperm and generative cells. Sexual Plant Reproduction, 9(5), 269-272. doi:10.1007/bf02152701 | es_ES |
dc.description.references | Stacey, N. J., Roberts, K., Carpita, N. C., Wells, B., & McCann, M. C. (1995). Dynamic changes in cell surface molecules are very early events in the differentiation of mesophyll cells from Zinnia elegans into tracheary elements. The Plant Journal, 8(6), 891-906. doi:10.1046/j.1365-313x.1995.8060891.x | es_ES |
dc.description.references | Tang, X.-C. (2006). The role of arabinogalactan proteins binding to Yariv reagents in the initiation, cell developmental fate, and maintenance of microspore embryogenesis in Brassica napus L. cv. Topas. Journal of Experimental Botany, 57(11), 2639-2650. doi:10.1093/jxb/erl027 | es_ES |
dc.description.references | Vaughn, K. C. (2003). Dodder hyphae invade the host: a structural and immunocytochemical characterization. Protoplasma, 220(3-4), 189-200. doi:10.1007/s00709-002-0038-3 | es_ES |
dc.description.references | Vaughn, K. C., Talbot, M. J., Offler, C. E., & McCurdy, D. W. (2006). Wall Ingrowths in Epidermal Transfer Cells of Vicia faba Cotyledons are Modified Primary Walls Marked by Localized Accumulations of Arabinogalactan Proteins. Plant and Cell Physiology, 48(1), 159-168. doi:10.1093/pcp/pcl047 | es_ES |
dc.description.references | Wilson, Z. A., Song, J., Taylor, B., & Yang, C. (2011). The final split: the regulation of anther dehiscence. Journal of Experimental Botany, 62(5), 1633-1649. doi:10.1093/jxb/err014 | es_ES |
dc.description.references | Willats, W. G. T., Limberg, G., Buchholt, H. C., van Alebeek, G.-J., Benen, J., Christensen, T. M. I. E., … Knox, J. P. (2000). Analysis of pectic epitopes recognised by hybridoma and phage display monoclonal antibodies using defined oligosaccharides, polysaccharides, and enzymatic degradation. Carbohydrate Research, 327(3), 309-320. doi:10.1016/s0008-6215(00)00039-2 | es_ES |
dc.description.references | Willats, W. G. T., Marcus, S. E., & Knox, J. P. (1998). Generation of a monoclonal antibody specific to (1→5)-α-l-arabinan. Carbohydrate Research, 308(1-2), 149-152. doi:10.1016/s0008-6215(98)00070-6 | es_ES |
dc.description.references | Willats, W. G. T., Orfila, C., Limberg, G., Buchholt, H. C., van Alebeek, G.-J. W. M., Voragen, A. G. J., … Knox, J. P. (2001). Modulation of the Degree and Pattern of Methyl-esterification of Pectic Homogalacturonan in Plant Cell Walls. Journal of Biological Chemistry, 276(22), 19404-19413. doi:10.1074/jbc.m011242200 | es_ES |
dc.description.references | Willats, W. G. T., Steele-King, C. G., Marcus, S. E., & Knox, J. P. (1999). Side chains of pectic polysaccharides are regulated in relation to cell proliferation and cell differentiation. The Plant Journal, 20(6), 619-628. doi:10.1046/j.1365-313x.1999.00629.x | es_ES |
dc.description.references | Williams M.A. (1977) Quantitative Methods in Biology (Practical Methods in Electron Microscopy, Vol 6, Part 2). North Holland/American Elsevier, Amsterdam. | es_ES |
dc.description.references | Wiśniewska, E., & Majewska-Sawka, A. (2006). Cell wall polysaccharides in differentiating anthers and pistils of Lolium perenne. Protoplasma, 228(1-3), 65-71. doi:10.1007/s00709-006-0175-1 | es_ES |
dc.description.references | Zhang, G. F., & Staehelin, L. A. (1992). Functional Compartmentation of the Golgi Apparatus of Plant Cells. Plant Physiology, 99(3), 1070-1083. doi:10.1104/pp.99.3.1070 | es_ES |