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Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3

BACKGROUND: Proteases represent one of the most abundant classes of enzymes in eukaryotes and are known to play key roles in many biological processes in plants. However, little is known about their functions in fruit ripening and disease resistance, which are unique to flowering plants and required...

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Autores principales: Wang, Weihao, Cai, Jianghua, Wang, Peiwen, Tian, Shiping, Qin, Guozheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341188/
https://www.ncbi.nlm.nih.gov/pubmed/28270225
http://dx.doi.org/10.1186/s13059-017-1178-2
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author Wang, Weihao
Cai, Jianghua
Wang, Peiwen
Tian, Shiping
Qin, Guozheng
author_facet Wang, Weihao
Cai, Jianghua
Wang, Peiwen
Tian, Shiping
Qin, Guozheng
author_sort Wang, Weihao
collection PubMed
description BACKGROUND: Proteases represent one of the most abundant classes of enzymes in eukaryotes and are known to play key roles in many biological processes in plants. However, little is known about their functions in fruit ripening and disease resistance, which are unique to flowering plants and required for seed maturation and dispersal. Elucidating the genetic mechanisms of fruit ripening and disease resistance is an important goal given the biological and dietary significance of fruit. RESULTS: Through expression profile analyses of genes encoding tomato (Solanum lycopersicum) cysteine proteases, we identify a number of genes whose expression increases during fruit ripening. RNA interference (RNAi)-mediated repression of SlVPE3, a vacuolar protease gene, results in alterations in fruit pigmentation, lycopene biosynthesis, and ethylene production, suggesting that SlVPE3 is necessary for normal fruit ripening. Surprisingly, the SlVPE3 RNAi fruit are more susceptible to the necrotrophic pathogen Botrytis cinerea. Quantitative proteomic analysis identified 314 proteins that differentially accumulate upon SlVPE3 silencing, including proteins associated with fruit ripening and disease resistance. To identify the direct SlVPE3 targets and mechanisms contributing to fungal pathogen resistance, we perform a screening of SlVPE3-interacting proteins using co-immunoprecipitation coupled with mass spectrometry. We show that SlVPE3 is required for the cleavage of the serine protease inhibitor KTI4, which contributes to resistance against the fungal pathogen B. cinerea. CONCLUSIONS: Our findings contribute to elucidating gene regulatory networks and mechanisms that control fruit ripening and disease resistance responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1178-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-53411882017-03-10 Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3 Wang, Weihao Cai, Jianghua Wang, Peiwen Tian, Shiping Qin, Guozheng Genome Biol Research BACKGROUND: Proteases represent one of the most abundant classes of enzymes in eukaryotes and are known to play key roles in many biological processes in plants. However, little is known about their functions in fruit ripening and disease resistance, which are unique to flowering plants and required for seed maturation and dispersal. Elucidating the genetic mechanisms of fruit ripening and disease resistance is an important goal given the biological and dietary significance of fruit. RESULTS: Through expression profile analyses of genes encoding tomato (Solanum lycopersicum) cysteine proteases, we identify a number of genes whose expression increases during fruit ripening. RNA interference (RNAi)-mediated repression of SlVPE3, a vacuolar protease gene, results in alterations in fruit pigmentation, lycopene biosynthesis, and ethylene production, suggesting that SlVPE3 is necessary for normal fruit ripening. Surprisingly, the SlVPE3 RNAi fruit are more susceptible to the necrotrophic pathogen Botrytis cinerea. Quantitative proteomic analysis identified 314 proteins that differentially accumulate upon SlVPE3 silencing, including proteins associated with fruit ripening and disease resistance. To identify the direct SlVPE3 targets and mechanisms contributing to fungal pathogen resistance, we perform a screening of SlVPE3-interacting proteins using co-immunoprecipitation coupled with mass spectrometry. We show that SlVPE3 is required for the cleavage of the serine protease inhibitor KTI4, which contributes to resistance against the fungal pathogen B. cinerea. CONCLUSIONS: Our findings contribute to elucidating gene regulatory networks and mechanisms that control fruit ripening and disease resistance responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1178-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-07 /pmc/articles/PMC5341188/ /pubmed/28270225 http://dx.doi.org/10.1186/s13059-017-1178-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Wang, Weihao
Cai, Jianghua
Wang, Peiwen
Tian, Shiping
Qin, Guozheng
Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title_full Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title_fullStr Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title_full_unstemmed Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title_short Post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease SlVPE3
title_sort post-transcriptional regulation of fruit ripening and disease resistance in tomato by the vacuolar protease slvpe3
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5341188/
https://www.ncbi.nlm.nih.gov/pubmed/28270225
http://dx.doi.org/10.1186/s13059-017-1178-2
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