Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bres, Cécile, Petit, Johann, Reynoud, Nicolas, Brocard, Lysiane, Marion, Didier, Lahaye, Marc, Bakan, Bénédicte, Rothan, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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
_version_ 1785108907476123648
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
work_keys_str_mv AT brescecile theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT petitjohann theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT reynoudnicolas theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT brocardlysiane theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT mariondidier theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT lahayemarc theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT bakanbenedicte theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT rothanchristophe theslshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT brescecile slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT petitjohann slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT reynoudnicolas slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT brocardlysiane slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT mariondidier slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT lahayemarc slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT bakanbenedicte slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit
AT rothanchristophe slshn2transcriptionfactorcontributestocuticleformationandepidermalpatterningintomatofruit