Cargando…

CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew

BACKGROUND: The development of CRISPR/Cas9 technology has facilitated targeted mutagenesis in an efficient and precise way. Previously, RNAi silencing of the susceptibility (S) gene PowderyMildewResistance 4 (PMR4) in tomato has been shown to enhance resistance against the powdery mildew pathogen Oi...

Descripción completa

Detalles Bibliográficos
Autores principales: Santillán Martínez, Miguel I., Bracuto, Valentina, Koseoglou, Eleni, Appiano, Michela, Jacobsen, Evert, Visser, Richard G. F., Wolters, Anne-Marie A., Bai, Yuling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304142/
https://www.ncbi.nlm.nih.gov/pubmed/32560695
http://dx.doi.org/10.1186/s12870-020-02497-y
_version_ 1783548206450212864
author Santillán Martínez, Miguel I.
Bracuto, Valentina
Koseoglou, Eleni
Appiano, Michela
Jacobsen, Evert
Visser, Richard G. F.
Wolters, Anne-Marie A.
Bai, Yuling
author_facet Santillán Martínez, Miguel I.
Bracuto, Valentina
Koseoglou, Eleni
Appiano, Michela
Jacobsen, Evert
Visser, Richard G. F.
Wolters, Anne-Marie A.
Bai, Yuling
author_sort Santillán Martínez, Miguel I.
collection PubMed
description BACKGROUND: The development of CRISPR/Cas9 technology has facilitated targeted mutagenesis in an efficient and precise way. Previously, RNAi silencing of the susceptibility (S) gene PowderyMildewResistance 4 (PMR4) in tomato has been shown to enhance resistance against the powdery mildew pathogen Oidium neolycopersici (On). RESULTS: To study whether full knock-out of the tomato PMR4 gene would result in a higher level of resistance than in the RNAi-silenced transgenic plants we generated tomato PMR4 CRISPR mutants. We used a CRISPR/Cas9 construct containing four single-guide RNAs (sgRNAs) targeting the tomato PMR4 gene to increase the possibility of large deletions in the mutants. After PCR-based selection and sequencing of transformants, we identified five different mutation events, including deletions from 4 to 900-bp, a 1-bp insertion and a 892-bp inversion. These mutants all showed reduced susceptibility to On based on visual scoring of disease symptoms and quantification of relative fungal biomass. Histological observations revealed a significantly higher occurrence of hypersensitive response-like cell death at sites of fungal infection in the pmr4 mutants compared to wild-type plants. Both haustorial formation and hyphal growth were diminished but not completely inhibited in the mutants. CONCLUSION: CRISPR/Cas-9 targeted mutagenesis of the tomato PMR4 gene resulted in mutants with reduced but not complete loss of susceptibility to the PM pathogen On. Our study demonstrates the efficiency and versatility of the CRISPR/Cas9 system as a powerful tool to study and characterize S-genes by generating different types of mutations.
format Online
Article
Text
id pubmed-7304142
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-73041422020-06-22 CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew Santillán Martínez, Miguel I. Bracuto, Valentina Koseoglou, Eleni Appiano, Michela Jacobsen, Evert Visser, Richard G. F. Wolters, Anne-Marie A. Bai, Yuling BMC Plant Biol Research Article BACKGROUND: The development of CRISPR/Cas9 technology has facilitated targeted mutagenesis in an efficient and precise way. Previously, RNAi silencing of the susceptibility (S) gene PowderyMildewResistance 4 (PMR4) in tomato has been shown to enhance resistance against the powdery mildew pathogen Oidium neolycopersici (On). RESULTS: To study whether full knock-out of the tomato PMR4 gene would result in a higher level of resistance than in the RNAi-silenced transgenic plants we generated tomato PMR4 CRISPR mutants. We used a CRISPR/Cas9 construct containing four single-guide RNAs (sgRNAs) targeting the tomato PMR4 gene to increase the possibility of large deletions in the mutants. After PCR-based selection and sequencing of transformants, we identified five different mutation events, including deletions from 4 to 900-bp, a 1-bp insertion and a 892-bp inversion. These mutants all showed reduced susceptibility to On based on visual scoring of disease symptoms and quantification of relative fungal biomass. Histological observations revealed a significantly higher occurrence of hypersensitive response-like cell death at sites of fungal infection in the pmr4 mutants compared to wild-type plants. Both haustorial formation and hyphal growth were diminished but not completely inhibited in the mutants. CONCLUSION: CRISPR/Cas-9 targeted mutagenesis of the tomato PMR4 gene resulted in mutants with reduced but not complete loss of susceptibility to the PM pathogen On. Our study demonstrates the efficiency and versatility of the CRISPR/Cas9 system as a powerful tool to study and characterize S-genes by generating different types of mutations. BioMed Central 2020-06-19 /pmc/articles/PMC7304142/ /pubmed/32560695 http://dx.doi.org/10.1186/s12870-020-02497-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Santillán Martínez, Miguel I.
Bracuto, Valentina
Koseoglou, Eleni
Appiano, Michela
Jacobsen, Evert
Visser, Richard G. F.
Wolters, Anne-Marie A.
Bai, Yuling
CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title_full CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title_fullStr CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title_full_unstemmed CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title_short CRISPR/Cas9-targeted mutagenesis of the tomato susceptibility gene PMR4 for resistance against powdery mildew
title_sort crispr/cas9-targeted mutagenesis of the tomato susceptibility gene pmr4 for resistance against powdery mildew
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304142/
https://www.ncbi.nlm.nih.gov/pubmed/32560695
http://dx.doi.org/10.1186/s12870-020-02497-y
work_keys_str_mv AT santillanmartinezmigueli crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT bracutovalentina crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT koseogloueleni crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT appianomichela crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT jacobsenevert crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT visserrichardgf crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT woltersannemariea crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew
AT baiyuling crisprcas9targetedmutagenesisofthetomatosusceptibilitygenepmr4forresistanceagainstpowderymildew