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The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit
Tomato (Solanum lycopersicum) is an established model for studying plant cuticle because of its thick cuticle covering and embedding the epidermal cells of the fruit. In this study, we screened an EMS mutant collection of the miniature tomato cultivar Micro-Tom for fruit cracking mutants and found a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515250/ https://www.ncbi.nlm.nih.gov/pubmed/37789465 http://dx.doi.org/10.1186/s43897-022-00035-y |
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author | Bres, Cécile Petit, Johann Reynoud, Nicolas Brocard, Lysiane Marion, Didier Lahaye, Marc Bakan, Bénédicte Rothan, Christophe |
author_facet | Bres, Cécile Petit, Johann Reynoud, Nicolas Brocard, Lysiane Marion, Didier Lahaye, Marc Bakan, Bénédicte Rothan, Christophe |
author_sort | Bres, Cécile |
collection | PubMed |
description | Tomato (Solanum lycopersicum) is an established model for studying plant cuticle because of its thick cuticle covering and embedding the epidermal cells of the fruit. In this study, we screened an EMS mutant collection of the miniature tomato cultivar Micro-Tom for fruit cracking mutants and found a mutant displaying a glossy fruit phenotype. By using an established mapping-by-sequencing strategy, we identified the causal mutation in the SlSHN2 transcription factor that is specifically expressed in outer epidermis of growing fruit. The point mutation in the shn2 mutant introduces a K to N amino acid change in the highly conserved ‘mm’ domain of SHN proteins. The cuticle from shn2 fruit showed a ~ fivefold reduction in cutin while abundance and composition of waxes were barely affected. In addition to alterations in cuticle thickness and properties, epidermal patterning and polysaccharide composition of the cuticle were changed. RNAseq analysis further highlighted the altered expression of hundreds of genes in the fruit exocarp of shn2, including genes associated with cuticle and cell wall formation, hormone signaling and response, and transcriptional regulation. In conclusion, we showed that a point mutation in the transcriptional regulator SlSHN2 causes major changes in fruit cuticle formation and its coordination with epidermal patterning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43897-022-00035-y. |
format | Online Article Text |
id | pubmed-10515250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105152502023-09-27 The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit Bres, Cécile Petit, Johann Reynoud, Nicolas Brocard, Lysiane Marion, Didier Lahaye, Marc Bakan, Bénédicte Rothan, Christophe Mol Hortic Research Article Tomato (Solanum lycopersicum) is an established model for studying plant cuticle because of its thick cuticle covering and embedding the epidermal cells of the fruit. In this study, we screened an EMS mutant collection of the miniature tomato cultivar Micro-Tom for fruit cracking mutants and found a mutant displaying a glossy fruit phenotype. By using an established mapping-by-sequencing strategy, we identified the causal mutation in the SlSHN2 transcription factor that is specifically expressed in outer epidermis of growing fruit. The point mutation in the shn2 mutant introduces a K to N amino acid change in the highly conserved ‘mm’ domain of SHN proteins. The cuticle from shn2 fruit showed a ~ fivefold reduction in cutin while abundance and composition of waxes were barely affected. In addition to alterations in cuticle thickness and properties, epidermal patterning and polysaccharide composition of the cuticle were changed. RNAseq analysis further highlighted the altered expression of hundreds of genes in the fruit exocarp of shn2, including genes associated with cuticle and cell wall formation, hormone signaling and response, and transcriptional regulation. In conclusion, we showed that a point mutation in the transcriptional regulator SlSHN2 causes major changes in fruit cuticle formation and its coordination with epidermal patterning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43897-022-00035-y. BioMed Central 2022-06-07 /pmc/articles/PMC10515250/ /pubmed/37789465 http://dx.doi.org/10.1186/s43897-022-00035-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Bres, Cécile Petit, Johann Reynoud, Nicolas Brocard, Lysiane Marion, Didier Lahaye, Marc Bakan, Bénédicte Rothan, Christophe The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title | The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title_full | The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title_fullStr | The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title_full_unstemmed | The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title_short | The SlSHN2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
title_sort | slshn2 transcription factor contributes to cuticle formation and epidermal patterning in tomato fruit |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515250/ https://www.ncbi.nlm.nih.gov/pubmed/37789465 http://dx.doi.org/10.1186/s43897-022-00035-y |
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