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uORF-mediated translation allows engineered plant disease resistance without fitness costs

Controlling plant disease has been a struggle for mankind since the advent of agriculture. Studies of plant immune mechanisms have led to strategies of engineering resistant crops through ectopic transcription of plants’ own defence genes, such as the master immune regulatory gene NPR1(1). However,...

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Autores principales: Xu, Guoyong, Yuan, Meng, Ai, Chaoren, Liu, Lijing, Zhuang, Edward, Karapetyan, Sargis, Wang, Shiping, Dong, Xinnian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532539/
https://www.ncbi.nlm.nih.gov/pubmed/28514448
http://dx.doi.org/10.1038/nature22372
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author Xu, Guoyong
Yuan, Meng
Ai, Chaoren
Liu, Lijing
Zhuang, Edward
Karapetyan, Sargis
Wang, Shiping
Dong, Xinnian
author_facet Xu, Guoyong
Yuan, Meng
Ai, Chaoren
Liu, Lijing
Zhuang, Edward
Karapetyan, Sargis
Wang, Shiping
Dong, Xinnian
author_sort Xu, Guoyong
collection PubMed
description Controlling plant disease has been a struggle for mankind since the advent of agriculture. Studies of plant immune mechanisms have led to strategies of engineering resistant crops through ectopic transcription of plants’ own defence genes, such as the master immune regulatory gene NPR1(1). However, enhanced resistance obtained through such strategies is often associated with significant penalties to fitness(2), making the resulting products undesirable for agricultural applications. To remedy this problem, we sought more stringent mechanisms of expressing defence proteins. Based on our latest finding that translation of key immune regulators, such as TBF1(3), is rapidly and transiently induced upon pathogen challenge (accompanying manuscript), we developed “TBF1-cassette” consisting of not only the immune-inducible promoter but also two pathogen-responsive upstream open reading frames (uORFs(TBF1)) of the TBF1 gene. We demonstrate that inclusion of the uORFs(TBF1)-mediated translational control over the production of snc1 (an autoactivated immune receptor) in Arabidopsis (At) and AtNPR1 in rice enables us to engineer broad-spectrum disease resistance without compromising plant fitness in the laboratory or in the field. This broadly applicable new strategy may lead to reduced use of pesticides and lightening of selective pressure for resistant pathogens.
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spelling pubmed-55325392017-11-17 uORF-mediated translation allows engineered plant disease resistance without fitness costs Xu, Guoyong Yuan, Meng Ai, Chaoren Liu, Lijing Zhuang, Edward Karapetyan, Sargis Wang, Shiping Dong, Xinnian Nature Article Controlling plant disease has been a struggle for mankind since the advent of agriculture. Studies of plant immune mechanisms have led to strategies of engineering resistant crops through ectopic transcription of plants’ own defence genes, such as the master immune regulatory gene NPR1(1). However, enhanced resistance obtained through such strategies is often associated with significant penalties to fitness(2), making the resulting products undesirable for agricultural applications. To remedy this problem, we sought more stringent mechanisms of expressing defence proteins. Based on our latest finding that translation of key immune regulators, such as TBF1(3), is rapidly and transiently induced upon pathogen challenge (accompanying manuscript), we developed “TBF1-cassette” consisting of not only the immune-inducible promoter but also two pathogen-responsive upstream open reading frames (uORFs(TBF1)) of the TBF1 gene. We demonstrate that inclusion of the uORFs(TBF1)-mediated translational control over the production of snc1 (an autoactivated immune receptor) in Arabidopsis (At) and AtNPR1 in rice enables us to engineer broad-spectrum disease resistance without compromising plant fitness in the laboratory or in the field. This broadly applicable new strategy may lead to reduced use of pesticides and lightening of selective pressure for resistant pathogens. 2017-05-17 2017-05-25 /pmc/articles/PMC5532539/ /pubmed/28514448 http://dx.doi.org/10.1038/nature22372 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms Reprints and permissions information is available at www.nature.com/reprints.
spellingShingle Article
Xu, Guoyong
Yuan, Meng
Ai, Chaoren
Liu, Lijing
Zhuang, Edward
Karapetyan, Sargis
Wang, Shiping
Dong, Xinnian
uORF-mediated translation allows engineered plant disease resistance without fitness costs
title uORF-mediated translation allows engineered plant disease resistance without fitness costs
title_full uORF-mediated translation allows engineered plant disease resistance without fitness costs
title_fullStr uORF-mediated translation allows engineered plant disease resistance without fitness costs
title_full_unstemmed uORF-mediated translation allows engineered plant disease resistance without fitness costs
title_short uORF-mediated translation allows engineered plant disease resistance without fitness costs
title_sort uorf-mediated translation allows engineered plant disease resistance without fitness costs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532539/
https://www.ncbi.nlm.nih.gov/pubmed/28514448
http://dx.doi.org/10.1038/nature22372
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