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CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca
Broomrapes (Phelipanche aegyptiaca and Orobanche spp.) are obligate plant parasites that cause extreme damage to crop plants. The parasite seeds have strict requirements for germination, involving preconditioning and exposure to specific chemicals strigolactones [SLs] exuded by the host roots. SLs a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685993/ https://www.ncbi.nlm.nih.gov/pubmed/31391538 http://dx.doi.org/10.1038/s41598-019-47893-z |
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author | Bari, Vinay Kumar Nassar, Jackline Abu Kheredin, Sally Marzouk Gal-On, Amit Ron, Mily Britt, Anne Steele, Daniel Yoder, John Aly, Radi |
author_facet | Bari, Vinay Kumar Nassar, Jackline Abu Kheredin, Sally Marzouk Gal-On, Amit Ron, Mily Britt, Anne Steele, Daniel Yoder, John Aly, Radi |
author_sort | Bari, Vinay Kumar |
collection | PubMed |
description | Broomrapes (Phelipanche aegyptiaca and Orobanche spp.) are obligate plant parasites that cause extreme damage to crop plants. The parasite seeds have strict requirements for germination, involving preconditioning and exposure to specific chemicals strigolactones [SLs] exuded by the host roots. SLs are plant hormones derived from plant carotenoids via a pathway involving the Carotenoid Cleavage Dioxygenase 8 (CCD8). Having no effective means to control parasitic weeds in most crops, and with CRISPR/Cas9 being an effective gene-editing tool, here we demonstrate that CRISPR/Cas9-mediated mutagenesis of the CCD8 gene can be used to develop host resistance to the parasitic weed P. aegyptiaca. Cas9/single guide (sg) RNA constructs were targeted to the second exon of CCD8 in tomato (Solanum lycopersicum L.) plants. Several (CCD8)Cas9 mutated tomato lines with variable insertions or deletions in CCD8 were obtained with no identified off-targets. Genotype analysis of T1 plants showed that the introduced CCD8 mutations are inherited. Compared to control tomato plants, the (CCD8)Cas9 mutant had morphological changes that included dwarfing, excessive shoot branching and adventitious root formation. In addition, SL-deficient (CCD8)Cas9 mutants showed a significant reduction in parasite infestation compared to non-mutated tomato plants. In the (CCD8)Cas9 mutated lines, orobanchol (SL) content was significantly reduced but total carotenoids level and expression of genes related to carotenoid biosynthesis were increased, as compared to control plants. Taking into account, the impact of plant parasitic weeds on agriculture and difficulty to constitute efficient control methods, the current study offers insights into the development of a new, efficient method that could be combined with various collections of resistant tomato rootstocks. |
format | Online Article Text |
id | pubmed-6685993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66859932019-08-12 CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca Bari, Vinay Kumar Nassar, Jackline Abu Kheredin, Sally Marzouk Gal-On, Amit Ron, Mily Britt, Anne Steele, Daniel Yoder, John Aly, Radi Sci Rep Article Broomrapes (Phelipanche aegyptiaca and Orobanche spp.) are obligate plant parasites that cause extreme damage to crop plants. The parasite seeds have strict requirements for germination, involving preconditioning and exposure to specific chemicals strigolactones [SLs] exuded by the host roots. SLs are plant hormones derived from plant carotenoids via a pathway involving the Carotenoid Cleavage Dioxygenase 8 (CCD8). Having no effective means to control parasitic weeds in most crops, and with CRISPR/Cas9 being an effective gene-editing tool, here we demonstrate that CRISPR/Cas9-mediated mutagenesis of the CCD8 gene can be used to develop host resistance to the parasitic weed P. aegyptiaca. Cas9/single guide (sg) RNA constructs were targeted to the second exon of CCD8 in tomato (Solanum lycopersicum L.) plants. Several (CCD8)Cas9 mutated tomato lines with variable insertions or deletions in CCD8 were obtained with no identified off-targets. Genotype analysis of T1 plants showed that the introduced CCD8 mutations are inherited. Compared to control tomato plants, the (CCD8)Cas9 mutant had morphological changes that included dwarfing, excessive shoot branching and adventitious root formation. In addition, SL-deficient (CCD8)Cas9 mutants showed a significant reduction in parasite infestation compared to non-mutated tomato plants. In the (CCD8)Cas9 mutated lines, orobanchol (SL) content was significantly reduced but total carotenoids level and expression of genes related to carotenoid biosynthesis were increased, as compared to control plants. Taking into account, the impact of plant parasitic weeds on agriculture and difficulty to constitute efficient control methods, the current study offers insights into the development of a new, efficient method that could be combined with various collections of resistant tomato rootstocks. Nature Publishing Group UK 2019-08-07 /pmc/articles/PMC6685993/ /pubmed/31391538 http://dx.doi.org/10.1038/s41598-019-47893-z Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bari, Vinay Kumar Nassar, Jackline Abu Kheredin, Sally Marzouk Gal-On, Amit Ron, Mily Britt, Anne Steele, Daniel Yoder, John Aly, Radi CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title | CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title_full | CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title_fullStr | CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title_full_unstemmed | CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title_short | CRISPR/Cas9-mediated mutagenesis of CAROTENOID CLEAVAGE DIOXYGENASE8 in tomato provides resistance against the parasitic weed Phelipanche aegyptiaca |
title_sort | crispr/cas9-mediated mutagenesis of carotenoid cleavage dioxygenase8 in tomato provides resistance against the parasitic weed phelipanche aegyptiaca |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685993/ https://www.ncbi.nlm.nih.gov/pubmed/31391538 http://dx.doi.org/10.1038/s41598-019-47893-z |
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