Cargando…
The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato
Although production of tomato (Solanum lycopersicum) is threatened by a number of major diseases worldwide, it has been difficult to identify effective and durable management measures against these diseases. In this study, we attempted to improve tomato disease resistance by transgenic overexpressio...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066517/ https://www.ncbi.nlm.nih.gov/pubmed/30087688 http://dx.doi.org/10.3389/fpls.2018.01066 |
_version_ | 1783342972714090496 |
---|---|
author | Pereira, Juliana A. Yu, Fahong Zhang, Yanping Jones, Jeffrey B. Mou, Zhonglin |
author_facet | Pereira, Juliana A. Yu, Fahong Zhang, Yanping Jones, Jeffrey B. Mou, Zhonglin |
author_sort | Pereira, Juliana A. |
collection | PubMed |
description | Although production of tomato (Solanum lycopersicum) is threatened by a number of major diseases worldwide, it has been difficult to identify effective and durable management measures against these diseases. In this study, we attempted to improve tomato disease resistance by transgenic overexpression of genes encoding the Arabidopsis thaliana Elongator (AtELP) complex subunits AtELP3 and AtELP4. We show that overexpression of AtELP3 and AtELP4 significantly enhanced resistance to tomato bacterial speck caused by the Pseudomonas syringae pv. tomato strain J4 (Pst J4) without clear detrimental effects on plant growth and development. Interestingly, the transgenic plants exhibited resistance to Pst J4 only when inoculated through foliar sprays but not through infiltration into the leaf apoplast. Although this result suggested possible involvement of stomatal immunity, we found that Pst J4 inoculation did not induce stomatal closure and there were no differences in stomatal apertures and conductance between the transgenic and control plants. Further RNA sequencing and real-time quantitative PCR analyses revealed a group of defense-related genes to be induced to higher levels after infection in the AtELP4 transgenic tomato plants than in the control, suggesting that the enhanced disease resistance of the transgenic plants may be attributed to elevated induction of defense responses. Additionally, we show that the tomato genome contains single-copy genes encoding all six Elongator subunits (SlELPs), which share high identities with the AtELP proteins, and that SlELP3 and SlELP4 complemented the Arabidopsis Atelp3 and Atelp4 mutants, respectively, indicating that the function of tomato Elongator is probably conserved. Taken together, our results not only shed new light on the tomato Elongator complex, but also revealed potential candidate genes for engineering disease resistance in tomato. |
format | Online Article Text |
id | pubmed-6066517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60665172018-08-07 The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato Pereira, Juliana A. Yu, Fahong Zhang, Yanping Jones, Jeffrey B. Mou, Zhonglin Front Plant Sci Plant Science Although production of tomato (Solanum lycopersicum) is threatened by a number of major diseases worldwide, it has been difficult to identify effective and durable management measures against these diseases. In this study, we attempted to improve tomato disease resistance by transgenic overexpression of genes encoding the Arabidopsis thaliana Elongator (AtELP) complex subunits AtELP3 and AtELP4. We show that overexpression of AtELP3 and AtELP4 significantly enhanced resistance to tomato bacterial speck caused by the Pseudomonas syringae pv. tomato strain J4 (Pst J4) without clear detrimental effects on plant growth and development. Interestingly, the transgenic plants exhibited resistance to Pst J4 only when inoculated through foliar sprays but not through infiltration into the leaf apoplast. Although this result suggested possible involvement of stomatal immunity, we found that Pst J4 inoculation did not induce stomatal closure and there were no differences in stomatal apertures and conductance between the transgenic and control plants. Further RNA sequencing and real-time quantitative PCR analyses revealed a group of defense-related genes to be induced to higher levels after infection in the AtELP4 transgenic tomato plants than in the control, suggesting that the enhanced disease resistance of the transgenic plants may be attributed to elevated induction of defense responses. Additionally, we show that the tomato genome contains single-copy genes encoding all six Elongator subunits (SlELPs), which share high identities with the AtELP proteins, and that SlELP3 and SlELP4 complemented the Arabidopsis Atelp3 and Atelp4 mutants, respectively, indicating that the function of tomato Elongator is probably conserved. Taken together, our results not only shed new light on the tomato Elongator complex, but also revealed potential candidate genes for engineering disease resistance in tomato. Frontiers Media S.A. 2018-07-24 /pmc/articles/PMC6066517/ /pubmed/30087688 http://dx.doi.org/10.3389/fpls.2018.01066 Text en Copyright © 2018 Pereira, Yu, Zhang, Jones and Mou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Pereira, Juliana A. Yu, Fahong Zhang, Yanping Jones, Jeffrey B. Mou, Zhonglin The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title | The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title_full | The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title_fullStr | The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title_full_unstemmed | The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title_short | The Arabidopsis Elongator Subunit ELP3 and ELP4 Confer Resistance to Bacterial Speck in Tomato |
title_sort | arabidopsis elongator subunit elp3 and elp4 confer resistance to bacterial speck in tomato |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066517/ https://www.ncbi.nlm.nih.gov/pubmed/30087688 http://dx.doi.org/10.3389/fpls.2018.01066 |
work_keys_str_mv | AT pereirajulianaa thearabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT yufahong thearabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT zhangyanping thearabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT jonesjeffreyb thearabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT mouzhonglin thearabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT pereirajulianaa arabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT yufahong arabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT zhangyanping arabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT jonesjeffreyb arabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato AT mouzhonglin arabidopsiselongatorsubunitelp3andelp4conferresistancetobacterialspeckintomato |