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Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity

Plant–pathogen interactions are complex associations driven by the interplay of host and microbe‐encoded factors. With secreted pathogen proteins (effectors) and immune signalling components found in the plant nucleus, this compartment is a battleground where susceptibility is specified. We hypothes...

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Autores principales: Howden, Andrew J. M., Stam, Remco, Martinez Heredia, Victor, Motion, Graham B., ten Have, Sara, Hodge, Kelly, Marques Monteiro Amaro, Tiago M., Huitema, Edgar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637918/
https://www.ncbi.nlm.nih.gov/pubmed/28394025
http://dx.doi.org/10.1111/nph.14540
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author Howden, Andrew J. M.
Stam, Remco
Martinez Heredia, Victor
Motion, Graham B.
ten Have, Sara
Hodge, Kelly
Marques Monteiro Amaro, Tiago M.
Huitema, Edgar
author_facet Howden, Andrew J. M.
Stam, Remco
Martinez Heredia, Victor
Motion, Graham B.
ten Have, Sara
Hodge, Kelly
Marques Monteiro Amaro, Tiago M.
Huitema, Edgar
author_sort Howden, Andrew J. M.
collection PubMed
description Plant–pathogen interactions are complex associations driven by the interplay of host and microbe‐encoded factors. With secreted pathogen proteins (effectors) and immune signalling components found in the plant nucleus, this compartment is a battleground where susceptibility is specified. We hypothesized that, by defining changes in the nuclear proteome during infection, we can pinpoint vital components required for immunity or susceptibility. We tested this hypothesis by documenting dynamic changes in the tomato (Solanum lycopersicum) nuclear proteome during infection by the oomycete pathogen Phytophthora capsici. We enriched nuclei from infected and noninfected tissues and quantitatively assessed changes in the nuclear proteome. We then tested the role of candidate regulators in immunity through functional assays. We demonstrated that the host nuclear proteome dynamically changes during P. capsici infection. We observed that known nuclear immunity factors were differentially expressed and, based on this observation, selected a set of candidate regulators that we successfully implicated in immunity to P. capsici. Our work exemplifies a powerful strategy to gain rapid insight into important nuclear processes that underpin complex crop traits such as resistance. We have identified a large set of candidate nuclear factors that may underpin immunity to pathogens in crops.
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spelling pubmed-56379182017-10-25 Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity Howden, Andrew J. M. Stam, Remco Martinez Heredia, Victor Motion, Graham B. ten Have, Sara Hodge, Kelly Marques Monteiro Amaro, Tiago M. Huitema, Edgar New Phytol Research Plant–pathogen interactions are complex associations driven by the interplay of host and microbe‐encoded factors. With secreted pathogen proteins (effectors) and immune signalling components found in the plant nucleus, this compartment is a battleground where susceptibility is specified. We hypothesized that, by defining changes in the nuclear proteome during infection, we can pinpoint vital components required for immunity or susceptibility. We tested this hypothesis by documenting dynamic changes in the tomato (Solanum lycopersicum) nuclear proteome during infection by the oomycete pathogen Phytophthora capsici. We enriched nuclei from infected and noninfected tissues and quantitatively assessed changes in the nuclear proteome. We then tested the role of candidate regulators in immunity through functional assays. We demonstrated that the host nuclear proteome dynamically changes during P. capsici infection. We observed that known nuclear immunity factors were differentially expressed and, based on this observation, selected a set of candidate regulators that we successfully implicated in immunity to P. capsici. Our work exemplifies a powerful strategy to gain rapid insight into important nuclear processes that underpin complex crop traits such as resistance. We have identified a large set of candidate nuclear factors that may underpin immunity to pathogens in crops. John Wiley and Sons Inc. 2017-04-10 2017-07 /pmc/articles/PMC5637918/ /pubmed/28394025 http://dx.doi.org/10.1111/nph.14540 Text en © 2017 The Authors. New Phytologist © 2017 New Phytologist Trust This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Howden, Andrew J. M.
Stam, Remco
Martinez Heredia, Victor
Motion, Graham B.
ten Have, Sara
Hodge, Kelly
Marques Monteiro Amaro, Tiago M.
Huitema, Edgar
Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title_full Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title_fullStr Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title_full_unstemmed Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title_short Quantitative analysis of the tomato nuclear proteome during Phytophthora capsici infection unveils regulators of immunity
title_sort quantitative analysis of the tomato nuclear proteome during phytophthora capsici infection unveils regulators of immunity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637918/
https://www.ncbi.nlm.nih.gov/pubmed/28394025
http://dx.doi.org/10.1111/nph.14540
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