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Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development

BACKGROUND: 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 m...

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Autores principales: Sala, Katarzyna, Malarz, Katarzyna, Barlow, Peter W., Kurczyńska, Ewa U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5267361/
https://www.ncbi.nlm.nih.gov/pubmed/28122511
http://dx.doi.org/10.1186/s12870-016-0949-3
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author Sala, Katarzyna
Malarz, Katarzyna
Barlow, Peter W.
Kurczyńska, Ewa U.
author_facet Sala, Katarzyna
Malarz, Katarzyna
Barlow, Peter W.
Kurczyńska, Ewa U.
author_sort Sala, Katarzyna
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-52673612017-02-01 Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development Sala, Katarzyna Malarz, Katarzyna Barlow, Peter W. Kurczyńska, Ewa U. BMC Plant Biol Research Article BACKGROUND: 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. BioMed Central 2017-01-25 /pmc/articles/PMC5267361/ /pubmed/28122511 http://dx.doi.org/10.1186/s12870-016-0949-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sala, Katarzyna
Malarz, Katarzyna
Barlow, Peter W.
Kurczyńska, Ewa U.
Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title_full Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title_fullStr Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title_full_unstemmed Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title_short Distribution of some pectic and arabinogalactan protein epitopes during Solanum lycopersicum (L.) adventitious root development
title_sort distribution of some pectic and arabinogalactan protein epitopes during solanum lycopersicum (l.) adventitious root development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5267361/
https://www.ncbi.nlm.nih.gov/pubmed/28122511
http://dx.doi.org/10.1186/s12870-016-0949-3
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