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Time course of changes in the transcriptome during russet induction in apple fruit

BACKGROUND: Russeting is a major problem in many fruit crops. Russeting is caused by environmental factors such as wounding or moisture exposure of the fruit surface. Despite extensive research, the molecular sequence that triggers russet initiation remains unclear. Here, we present high-resolution...

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Autores principales: Straube, Jannis, Suvarna, Shreya, Chen, Yun-Hao, Khanal, Bishnu P., Knoche, Moritz, Debener, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542230/
https://www.ncbi.nlm.nih.gov/pubmed/37775771
http://dx.doi.org/10.1186/s12870-023-04483-6
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author Straube, Jannis
Suvarna, Shreya
Chen, Yun-Hao
Khanal, Bishnu P.
Knoche, Moritz
Debener, Thomas
author_facet Straube, Jannis
Suvarna, Shreya
Chen, Yun-Hao
Khanal, Bishnu P.
Knoche, Moritz
Debener, Thomas
author_sort Straube, Jannis
collection PubMed
description BACKGROUND: Russeting is a major problem in many fruit crops. Russeting is caused by environmental factors such as wounding or moisture exposure of the fruit surface. Despite extensive research, the molecular sequence that triggers russet initiation remains unclear. Here, we present high-resolution transcriptomic data by controlled russet induction at very early stages of fruit development. During Phase I, a patch of the fruit surface is exposed to surface moisture. For Phase II, moisture exposure is terminated, and the formerly exposed surface remains dry. We targeted differentially expressed transcripts as soon as 24 h after russet induction. RESULTS: During moisture exposure (Phase I) of ‘Pinova’ apple, transcripts associated with the cell cycle, cell wall, and cuticle synthesis (SHN3) decrease, while those related to abiotic stress increase. NAC35 and MYB17 were the earliest induced genes during Phase I. They are therefore linked to the initial processes of cuticle microcracking. After moisture removal (Phase II), the expression of genes related to meristematic activity increased (WOX4 within 24 h, MYB84 within 48 h). Genes related to lignin synthesis (MYB52) and suberin synthesis (MYB93, WRKY56) were upregulated within 3 d after moisture removal. WOX4 and AP2B3 are the earliest differentially expressed genes induced in Phase II. They are therefore linked to early events in periderm formation. The expression profiles were consistent between two different seasons and mirrored differences in russet susceptibility in a comparison of cultivars. Furthermore, expression profiles during Phase II of moisture induction were largely identical to those following wounding. CONCLUSIONS: The combination of a unique controlled russet induction technique with high-resolution transcriptomic data allowed for the very first time to analyse the formation of cuticular microcracks and periderm in apple fruit immediately after the onset of triggering factors. This data provides valuable insights into the spatial-temporal dynamics of russeting, including the synthesis of cuticles, dedifferentiation of cells, and impregnation of cell walls with suberin and lignin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-023-04483-6.
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spelling pubmed-105422302023-10-03 Time course of changes in the transcriptome during russet induction in apple fruit Straube, Jannis Suvarna, Shreya Chen, Yun-Hao Khanal, Bishnu P. Knoche, Moritz Debener, Thomas BMC Plant Biol Research BACKGROUND: Russeting is a major problem in many fruit crops. Russeting is caused by environmental factors such as wounding or moisture exposure of the fruit surface. Despite extensive research, the molecular sequence that triggers russet initiation remains unclear. Here, we present high-resolution transcriptomic data by controlled russet induction at very early stages of fruit development. During Phase I, a patch of the fruit surface is exposed to surface moisture. For Phase II, moisture exposure is terminated, and the formerly exposed surface remains dry. We targeted differentially expressed transcripts as soon as 24 h after russet induction. RESULTS: During moisture exposure (Phase I) of ‘Pinova’ apple, transcripts associated with the cell cycle, cell wall, and cuticle synthesis (SHN3) decrease, while those related to abiotic stress increase. NAC35 and MYB17 were the earliest induced genes during Phase I. They are therefore linked to the initial processes of cuticle microcracking. After moisture removal (Phase II), the expression of genes related to meristematic activity increased (WOX4 within 24 h, MYB84 within 48 h). Genes related to lignin synthesis (MYB52) and suberin synthesis (MYB93, WRKY56) were upregulated within 3 d after moisture removal. WOX4 and AP2B3 are the earliest differentially expressed genes induced in Phase II. They are therefore linked to early events in periderm formation. The expression profiles were consistent between two different seasons and mirrored differences in russet susceptibility in a comparison of cultivars. Furthermore, expression profiles during Phase II of moisture induction were largely identical to those following wounding. CONCLUSIONS: The combination of a unique controlled russet induction technique with high-resolution transcriptomic data allowed for the very first time to analyse the formation of cuticular microcracks and periderm in apple fruit immediately after the onset of triggering factors. This data provides valuable insights into the spatial-temporal dynamics of russeting, including the synthesis of cuticles, dedifferentiation of cells, and impregnation of cell walls with suberin and lignin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-023-04483-6. BioMed Central 2023-09-30 /pmc/articles/PMC10542230/ /pubmed/37775771 http://dx.doi.org/10.1186/s12870-023-04483-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Straube, Jannis
Suvarna, Shreya
Chen, Yun-Hao
Khanal, Bishnu P.
Knoche, Moritz
Debener, Thomas
Time course of changes in the transcriptome during russet induction in apple fruit
title Time course of changes in the transcriptome during russet induction in apple fruit
title_full Time course of changes in the transcriptome during russet induction in apple fruit
title_fullStr Time course of changes in the transcriptome during russet induction in apple fruit
title_full_unstemmed Time course of changes in the transcriptome during russet induction in apple fruit
title_short Time course of changes in the transcriptome during russet induction in apple fruit
title_sort time course of changes in the transcriptome during russet induction in apple fruit
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10542230/
https://www.ncbi.nlm.nih.gov/pubmed/37775771
http://dx.doi.org/10.1186/s12870-023-04483-6
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