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Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation

BACKGROUND: Apple fruit mealiness is one of the most important textural problems that results from an undesirable ripening process during storage. This phenotype is characterized by textural deterioration described as soft, grainy and dry fruit. Despite several studies, little is known about mealine...

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Autores principales: Segonne, Sandrine Mikol, Bruneau, Maryline, Celton, Jean-Marc, Le Gall, Sophie, Francin-Allami, Mathilde, Juchaux, Marjorie, Laurens, François, Orsel, Mathilde, Renou, Jean-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310206/
https://www.ncbi.nlm.nih.gov/pubmed/25551767
http://dx.doi.org/10.1186/s12870-014-0375-3
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author Segonne, Sandrine Mikol
Bruneau, Maryline
Celton, Jean-Marc
Le Gall, Sophie
Francin-Allami, Mathilde
Juchaux, Marjorie
Laurens, François
Orsel, Mathilde
Renou, Jean-Pierre
author_facet Segonne, Sandrine Mikol
Bruneau, Maryline
Celton, Jean-Marc
Le Gall, Sophie
Francin-Allami, Mathilde
Juchaux, Marjorie
Laurens, François
Orsel, Mathilde
Renou, Jean-Pierre
author_sort Segonne, Sandrine Mikol
collection PubMed
description BACKGROUND: Apple fruit mealiness is one of the most important textural problems that results from an undesirable ripening process during storage. This phenotype is characterized by textural deterioration described as soft, grainy and dry fruit. Despite several studies, little is known about mealiness development and the associated molecular events. In this study, we integrated phenotypic, microscopic, transcriptomic and biochemical analyses to gain insights into the molecular basis of mealiness development. RESULTS: Instrumental texture characterization allowed the refinement of the definition of apple mealiness. In parallel, a new and simple quantitative test to assess this phenotype was developed. Six individuals with contrasting mealiness were selected among a progeny and used to perform a global transcriptome analysis during fruit development and cold storage. Potential candidate genes associated with the initiation of mealiness were identified. Amongst these, the expression profile of an early down-regulated transcript similar to an Arabidopsis thaliana pectin methylesterase gene (AtPME2) matched with mealiness development. In silico analyses of this Malus x domestica PME gene (MdPME2) confirmed its specific pattern compared with all other identified MdPME genes. Protein fusion experiments showed that MdPME2 is secreted into the apoplast in accordance with a possible activity on pectin structure. Further microscopic analysis indicated a progressive loss of cell to cell adhesion in mealy apple fruits. Biochemical analysis revealed specific modifications of pectin residues associated with mealiness, without global changes in the degree of methylesterification of pectins. CONCLUSIONS: These data support the role of PME in cell wall remodelling during apple fruit development and ripening and suggest a local action of these enzymes. Mealiness may partially result from qualitative and spatial variations of pectin microarchitecture rather than quantitative pectin differences, and these changes may occur early in fruit development. The specific MdPME2 gene highlighted in this study could be a good early marker of texture unfavourable trait in apple. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0375-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-43102062015-01-30 Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation Segonne, Sandrine Mikol Bruneau, Maryline Celton, Jean-Marc Le Gall, Sophie Francin-Allami, Mathilde Juchaux, Marjorie Laurens, François Orsel, Mathilde Renou, Jean-Pierre BMC Plant Biol Research Article BACKGROUND: Apple fruit mealiness is one of the most important textural problems that results from an undesirable ripening process during storage. This phenotype is characterized by textural deterioration described as soft, grainy and dry fruit. Despite several studies, little is known about mealiness development and the associated molecular events. In this study, we integrated phenotypic, microscopic, transcriptomic and biochemical analyses to gain insights into the molecular basis of mealiness development. RESULTS: Instrumental texture characterization allowed the refinement of the definition of apple mealiness. In parallel, a new and simple quantitative test to assess this phenotype was developed. Six individuals with contrasting mealiness were selected among a progeny and used to perform a global transcriptome analysis during fruit development and cold storage. Potential candidate genes associated with the initiation of mealiness were identified. Amongst these, the expression profile of an early down-regulated transcript similar to an Arabidopsis thaliana pectin methylesterase gene (AtPME2) matched with mealiness development. In silico analyses of this Malus x domestica PME gene (MdPME2) confirmed its specific pattern compared with all other identified MdPME genes. Protein fusion experiments showed that MdPME2 is secreted into the apoplast in accordance with a possible activity on pectin structure. Further microscopic analysis indicated a progressive loss of cell to cell adhesion in mealy apple fruits. Biochemical analysis revealed specific modifications of pectin residues associated with mealiness, without global changes in the degree of methylesterification of pectins. CONCLUSIONS: These data support the role of PME in cell wall remodelling during apple fruit development and ripening and suggest a local action of these enzymes. Mealiness may partially result from qualitative and spatial variations of pectin microarchitecture rather than quantitative pectin differences, and these changes may occur early in fruit development. The specific MdPME2 gene highlighted in this study could be a good early marker of texture unfavourable trait in apple. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0375-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-31 /pmc/articles/PMC4310206/ /pubmed/25551767 http://dx.doi.org/10.1186/s12870-014-0375-3 Text en © Segonne et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Segonne, Sandrine Mikol
Bruneau, Maryline
Celton, Jean-Marc
Le Gall, Sophie
Francin-Allami, Mathilde
Juchaux, Marjorie
Laurens, François
Orsel, Mathilde
Renou, Jean-Pierre
Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title_full Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title_fullStr Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title_full_unstemmed Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title_short Multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
title_sort multiscale investigation of mealiness in apple: an atypical role for a pectin methylesterase during fruit maturation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310206/
https://www.ncbi.nlm.nih.gov/pubmed/25551767
http://dx.doi.org/10.1186/s12870-014-0375-3
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