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Autophagy modulates the metabolism and growth of tomato fruit during development
Although autophagy is a conserved mechanism operating across eukaryotes, its effects on crops and especially their metabolism has received relatively little attention. Indeed, whilst a few recent studies have used systems biology tools to look at the consequences of lack of autophagy in maize these...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343920/ https://www.ncbi.nlm.nih.gov/pubmed/35928403 http://dx.doi.org/10.1093/hr/uhac129 |
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author | Alseekh, Saleh Zhu, Feng Vallarino, José G Sokolowska, Ewelina M Yoshida, Takuya Bergmann, Susan Wendenburg, Regina Bolze, Antje Skirycz, Aleksandra Avin-Wittenberg, Tamar Fernie, Alisdair R |
author_facet | Alseekh, Saleh Zhu, Feng Vallarino, José G Sokolowska, Ewelina M Yoshida, Takuya Bergmann, Susan Wendenburg, Regina Bolze, Antje Skirycz, Aleksandra Avin-Wittenberg, Tamar Fernie, Alisdair R |
author_sort | Alseekh, Saleh |
collection | PubMed |
description | Although autophagy is a conserved mechanism operating across eukaryotes, its effects on crops and especially their metabolism has received relatively little attention. Indeed, whilst a few recent studies have used systems biology tools to look at the consequences of lack of autophagy in maize these focused on leaf tissues rather than the kernels. Here we utilized RNA interference (RNAi) to generate tomato plants that were deficient in the autophagy-regulating protease ATG4. Plants displayed an early senescence phenotype yet relatively mild changes in the foliar metabolome and were characterized by a reduced fruit yield phenotype. Metabolite profiling indicated that metabolites of ATG4-RNAi tomato leaves just exhibited minor alterations while that of fruit displayed bigger difference compared to the WT. In detail, many primary metabolites exhibited decreases in the ATG4-RNAi lines, such as proline, tryptophan and phenylalanine, while the representative secondary metabolites (quinic acid and 3-trans-caffeoylquinic acid) were present at substantially higher levels in ATG4-RNAi green fruits than in WT. Moreover, transcriptome analysis indicated that the most prominent differences were in the significant upregulation of organelle degradation genes involved in the proteasome or chloroplast vesiculation pathways, which was further confirmed by the reduced levels of chloroplastic proteins in the proteomics data. Furthermore, integration analysis of the metabolome, transcriptome and proteome data indicated that ATG4 significantly affected the lipid metabolism, chlorophyll binding proteins and chloroplast biosynthesis. These data collectively lead us to propose a more sophisticated model to explain the cellular co-ordination of the process of autophagy. |
format | Online Article Text |
id | pubmed-9343920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93439202022-08-03 Autophagy modulates the metabolism and growth of tomato fruit during development Alseekh, Saleh Zhu, Feng Vallarino, José G Sokolowska, Ewelina M Yoshida, Takuya Bergmann, Susan Wendenburg, Regina Bolze, Antje Skirycz, Aleksandra Avin-Wittenberg, Tamar Fernie, Alisdair R Hortic Res Article Although autophagy is a conserved mechanism operating across eukaryotes, its effects on crops and especially their metabolism has received relatively little attention. Indeed, whilst a few recent studies have used systems biology tools to look at the consequences of lack of autophagy in maize these focused on leaf tissues rather than the kernels. Here we utilized RNA interference (RNAi) to generate tomato plants that were deficient in the autophagy-regulating protease ATG4. Plants displayed an early senescence phenotype yet relatively mild changes in the foliar metabolome and were characterized by a reduced fruit yield phenotype. Metabolite profiling indicated that metabolites of ATG4-RNAi tomato leaves just exhibited minor alterations while that of fruit displayed bigger difference compared to the WT. In detail, many primary metabolites exhibited decreases in the ATG4-RNAi lines, such as proline, tryptophan and phenylalanine, while the representative secondary metabolites (quinic acid and 3-trans-caffeoylquinic acid) were present at substantially higher levels in ATG4-RNAi green fruits than in WT. Moreover, transcriptome analysis indicated that the most prominent differences were in the significant upregulation of organelle degradation genes involved in the proteasome or chloroplast vesiculation pathways, which was further confirmed by the reduced levels of chloroplastic proteins in the proteomics data. Furthermore, integration analysis of the metabolome, transcriptome and proteome data indicated that ATG4 significantly affected the lipid metabolism, chlorophyll binding proteins and chloroplast biosynthesis. These data collectively lead us to propose a more sophisticated model to explain the cellular co-ordination of the process of autophagy. Oxford University Press 2022-06-13 /pmc/articles/PMC9343920/ /pubmed/35928403 http://dx.doi.org/10.1093/hr/uhac129 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nanjing Agricultural University https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Alseekh, Saleh Zhu, Feng Vallarino, José G Sokolowska, Ewelina M Yoshida, Takuya Bergmann, Susan Wendenburg, Regina Bolze, Antje Skirycz, Aleksandra Avin-Wittenberg, Tamar Fernie, Alisdair R Autophagy modulates the metabolism and growth of tomato fruit during development |
title | Autophagy modulates the metabolism and growth of tomato fruit during development |
title_full | Autophagy modulates the metabolism and growth of tomato fruit during development |
title_fullStr | Autophagy modulates the metabolism and growth of tomato fruit during development |
title_full_unstemmed | Autophagy modulates the metabolism and growth of tomato fruit during development |
title_short | Autophagy modulates the metabolism and growth of tomato fruit during development |
title_sort | autophagy modulates the metabolism and growth of tomato fruit during development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343920/ https://www.ncbi.nlm.nih.gov/pubmed/35928403 http://dx.doi.org/10.1093/hr/uhac129 |
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