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Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions
BACKGROUND: In order to get global molecular understanding of one of the most important crop diseases worldwide, we investigated compatible and incompatible interactions between Phytophthora infestans and potato (Solanum tuberosum). We used the two most field-resistant potato clones under Swedish gr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079953/ https://www.ncbi.nlm.nih.gov/pubmed/24947944 http://dx.doi.org/10.1186/1471-2164-15-497 |
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author | Ali, Ashfaq Alexandersson, Erik Sandin, Marianne Resjö, Svante Lenman, Marit Hedley, Pete Levander, Fredrik Andreasson, Erik |
author_facet | Ali, Ashfaq Alexandersson, Erik Sandin, Marianne Resjö, Svante Lenman, Marit Hedley, Pete Levander, Fredrik Andreasson, Erik |
author_sort | Ali, Ashfaq |
collection | PubMed |
description | BACKGROUND: In order to get global molecular understanding of one of the most important crop diseases worldwide, we investigated compatible and incompatible interactions between Phytophthora infestans and potato (Solanum tuberosum). We used the two most field-resistant potato clones under Swedish growing conditions, which have the greatest known local diversity of P. infestans populations, and a reference compatible cultivar. RESULTS: Quantitative label-free proteomics of 51 apoplastic secretome samples (PXD000435) in combination with genome-wide transcript analysis by 42 microarrays (E-MTAB-1515) were used to capture changes in protein abundance and gene expression at 6, 24 and 72 hours after inoculation with P. infestans. To aid mass spectrometry analysis we generated cultivar-specific RNA-seq data (E-MTAB-1712), which increased peptide identifications by 17%. Components induced only during incompatible interactions, which are candidates for hypersensitive response initiation, include a Kunitz-like protease inhibitor, transcription factors and an RCR3-like protein. More secreted proteins had lower abundance in the compatible interaction compared to the incompatible interactions. Based on this observation and because the well-characterized effector-target C14 protease follows this pattern, we suggest 40 putative effector targets. CONCLUSIONS: In summary, over 17000 transcripts and 1000 secreted proteins changed in abundance in at least one time point, illustrating the dynamics of plant responses to a hemibiotroph. Half of the differentially abundant proteins showed a corresponding change at the transcript level. Many putative hypersensitive and effector-target proteins were single representatives of large gene families. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-497) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4079953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40799532014-07-14 Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions Ali, Ashfaq Alexandersson, Erik Sandin, Marianne Resjö, Svante Lenman, Marit Hedley, Pete Levander, Fredrik Andreasson, Erik BMC Genomics Research Article BACKGROUND: In order to get global molecular understanding of one of the most important crop diseases worldwide, we investigated compatible and incompatible interactions between Phytophthora infestans and potato (Solanum tuberosum). We used the two most field-resistant potato clones under Swedish growing conditions, which have the greatest known local diversity of P. infestans populations, and a reference compatible cultivar. RESULTS: Quantitative label-free proteomics of 51 apoplastic secretome samples (PXD000435) in combination with genome-wide transcript analysis by 42 microarrays (E-MTAB-1515) were used to capture changes in protein abundance and gene expression at 6, 24 and 72 hours after inoculation with P. infestans. To aid mass spectrometry analysis we generated cultivar-specific RNA-seq data (E-MTAB-1712), which increased peptide identifications by 17%. Components induced only during incompatible interactions, which are candidates for hypersensitive response initiation, include a Kunitz-like protease inhibitor, transcription factors and an RCR3-like protein. More secreted proteins had lower abundance in the compatible interaction compared to the incompatible interactions. Based on this observation and because the well-characterized effector-target C14 protease follows this pattern, we suggest 40 putative effector targets. CONCLUSIONS: In summary, over 17000 transcripts and 1000 secreted proteins changed in abundance in at least one time point, illustrating the dynamics of plant responses to a hemibiotroph. Half of the differentially abundant proteins showed a corresponding change at the transcript level. Many putative hypersensitive and effector-target proteins were single representatives of large gene families. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-497) contains supplementary material, which is available to authorized users. BioMed Central 2014-06-19 /pmc/articles/PMC4079953/ /pubmed/24947944 http://dx.doi.org/10.1186/1471-2164-15-497 Text en © Ali et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article Ali, Ashfaq Alexandersson, Erik Sandin, Marianne Resjö, Svante Lenman, Marit Hedley, Pete Levander, Fredrik Andreasson, Erik Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title | Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title_full | Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title_fullStr | Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title_full_unstemmed | Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title_short | Quantitative proteomics and transcriptomics of potato in response to Phytophthora infestans in compatible and incompatible interactions |
title_sort | quantitative proteomics and transcriptomics of potato in response to phytophthora infestans in compatible and incompatible interactions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079953/ https://www.ncbi.nlm.nih.gov/pubmed/24947944 http://dx.doi.org/10.1186/1471-2164-15-497 |
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