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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12128/8737
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dc.contributor.authorSala, Katarzyna-
dc.contributor.authorMalarz, Katarzyna-
dc.contributor.authorBarlow, Peter W.-
dc.contributor.authorKurczyńska, Ewa-
dc.date.accessioned2019-04-04T09:20:08Z-
dc.date.available2019-04-04T09:20:08Z-
dc.date.issued2017-
dc.identifier.citationBMC Plant Biology (Online), 2017, vol. 17, art. no 25pl_PL
dc.identifier.issn1471-2229-
dc.identifier.urihttp://hdl.handle.net/20.500.12128/8737-
dc.description.abstractBackground: The adventitious roots (AR) of plants share the same function as primary and lateral roots (LR), although their development is mainly an adaptive reaction to stress conditions. Regeneration of grafted plants is often accompanied by AR formation thus making the grafting technique a good model for studying AR initiation and development and their means of emergence. Pectins and arabinogalactan proteins (AGP) are helpful markers of particular cellular events, such as programmed cell death (PCD), elongation, proliferation or other differentiation events that accompany AR development. However, little is known about the distribution of pectins and AGPs during AR ontogeny, either in the primordium or stem tissues from which AR arise or their correspondence with these events during LR formation. Results: AR were developed from different stem tissues such as parenchyma, xylem rays and the cambium, depending on the stem age and treatment (grafting versus cutting) of the parental tissue. Immunochemical analysis of the presence of pectic (LM8, LM19, LM20) and AGP (JIM8, JIM13, JIM16) epitopes in AR and AR-associated tissues showed differential, tissue-specific distributions of these epitopes. Two pectic epitopes (LM19, LM20) were developmentally regulated and the occurrence of the LM8 xylogalacturonan epitope in the root cap of the AR differed from other species described so far. AGP epitopes were abundantly present in the cytoplasmic compartments (mainly the tonoplast) and were correlated with the degree of cell vacuolisation. JIM8 and JIM13 epitopes were detected in the more advanced stages of primordium development, whereas the JIM16 epitope was present from the earliest division events of the initial AR cells. The comparison between AR and LR showed quantitative (AGP,) and qualitative (pectins) differences. Conclusion: The chemical compositions of adventitious and lateral root cells show differences that correlate with the different origins of these cells. In AR, developmental changes in the distribution of pectins and AGP suggest the turnover of wall compounds. Our data extend the knowledge about the distribution of pectin and AGP during non-embryogenic root development in a species that is important from an agronomic point of view.pl_PL
dc.language.isoenpl_PL
dc.rightsUznanie autorstwa 3.0 Polska*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/pl/*
dc.subjectarabinogalactan proteinspl_PL
dc.subjectautograftingpl_PL
dc.subjectcell differentiationpl_PL
dc.subjectcell wallpl_PL
dc.subjectimmunohistochemistrypl_PL
dc.subjectlateral rootspl_PL
dc.subjectpectinspl_PL
dc.subjecttomatoespl_PL
dc.titleDistribution of some pectic andarabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root developmentpl_PL
dc.typeinfo:eu-repo/semantics/articlepl_PL
dc.relation.journalBMC Plant Biology (Online)pl_PL
dc.identifier.doi10.1186/s12870-016-0949-3-
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