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Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight

Sugar content is one of the most important quality traits of tomato. Cell wall invertase promotes sucrose unloading in the fruit by maintaining a gradient of sucrose concentration between source leaves and fruits, while invertase inhibitor (INVINH) regulates this process. In this study, knock-out of...

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Autores principales: Kawaguchi, Kohei, Takei-Hoshi, Rie, Yoshikawa, Ikue, Nishida, Keiji, Kobayashi, Makoto, Kusano, Miyako, Lu, Yu, Ariizumi, Tohru, Ezura, Hiroshi, Otagaki, Shungo, Matsumoto, Shogo, Shiratake, Katsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563804/
https://www.ncbi.nlm.nih.gov/pubmed/34728724
http://dx.doi.org/10.1038/s41598-021-00966-4
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author Kawaguchi, Kohei
Takei-Hoshi, Rie
Yoshikawa, Ikue
Nishida, Keiji
Kobayashi, Makoto
Kusano, Miyako
Lu, Yu
Ariizumi, Tohru
Ezura, Hiroshi
Otagaki, Shungo
Matsumoto, Shogo
Shiratake, Katsuhiro
author_facet Kawaguchi, Kohei
Takei-Hoshi, Rie
Yoshikawa, Ikue
Nishida, Keiji
Kobayashi, Makoto
Kusano, Miyako
Lu, Yu
Ariizumi, Tohru
Ezura, Hiroshi
Otagaki, Shungo
Matsumoto, Shogo
Shiratake, Katsuhiro
author_sort Kawaguchi, Kohei
collection PubMed
description Sugar content is one of the most important quality traits of tomato. Cell wall invertase promotes sucrose unloading in the fruit by maintaining a gradient of sucrose concentration between source leaves and fruits, while invertase inhibitor (INVINH) regulates this process. In this study, knock-out of cell wall INVINH in tomato (SlINVINH1) was performed by genome editing using, CRISPR/Cas9 and Target-AID technologies. Most of the genome-edited lines set higher soluble solid content (SSC) fruit than the original cultivar ‘Suzukoma’, while fruit weight was different among the genome-edited lines. From these genome-edited lines, three lines (193–3, 199–2, and 247–2), whose SSC was significantly higher than ‘Suzukoma’ and fruit weight were almost the same as the original cultivar, were selected. The fruit weight and overall plant growth of the two lines were comparable to those of the original cultivar. In contrast, the fructose and glucose contents in the mature fruits of the two lines were significantly higher than those of the original cultivar. The mature fruits of genome edited line 193–3 showed the highest sugar content, and the fructose and glucose contents were 29% and 36% higher than that of the original cultivar, respectively. Whole genome sequence data showed no off-target mutations in the genome-edited lines. Non-target metabolome analysis of mature fruits revealed that fructose was the highest loading factor in principal component analysis (PCA) between the genome-edited line and the original cultivar, and no unexpected metabolites appeared in the genome-edited line. In this study, we succeeded in producing tomato lines with high sugar content without a decrease in fruit weight and deterioration of plant growth by knock-out of SlINVINH1 using genome editing technology. This study showed that functional disruption of SlINVINH1 is an effective approach to produce tomato cultivars with high sugar content.
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spelling pubmed-85638042021-11-04 Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight Kawaguchi, Kohei Takei-Hoshi, Rie Yoshikawa, Ikue Nishida, Keiji Kobayashi, Makoto Kusano, Miyako Lu, Yu Ariizumi, Tohru Ezura, Hiroshi Otagaki, Shungo Matsumoto, Shogo Shiratake, Katsuhiro Sci Rep Article Sugar content is one of the most important quality traits of tomato. Cell wall invertase promotes sucrose unloading in the fruit by maintaining a gradient of sucrose concentration between source leaves and fruits, while invertase inhibitor (INVINH) regulates this process. In this study, knock-out of cell wall INVINH in tomato (SlINVINH1) was performed by genome editing using, CRISPR/Cas9 and Target-AID technologies. Most of the genome-edited lines set higher soluble solid content (SSC) fruit than the original cultivar ‘Suzukoma’, while fruit weight was different among the genome-edited lines. From these genome-edited lines, three lines (193–3, 199–2, and 247–2), whose SSC was significantly higher than ‘Suzukoma’ and fruit weight were almost the same as the original cultivar, were selected. The fruit weight and overall plant growth of the two lines were comparable to those of the original cultivar. In contrast, the fructose and glucose contents in the mature fruits of the two lines were significantly higher than those of the original cultivar. The mature fruits of genome edited line 193–3 showed the highest sugar content, and the fructose and glucose contents were 29% and 36% higher than that of the original cultivar, respectively. Whole genome sequence data showed no off-target mutations in the genome-edited lines. Non-target metabolome analysis of mature fruits revealed that fructose was the highest loading factor in principal component analysis (PCA) between the genome-edited line and the original cultivar, and no unexpected metabolites appeared in the genome-edited line. In this study, we succeeded in producing tomato lines with high sugar content without a decrease in fruit weight and deterioration of plant growth by knock-out of SlINVINH1 using genome editing technology. This study showed that functional disruption of SlINVINH1 is an effective approach to produce tomato cultivars with high sugar content. Nature Publishing Group UK 2021-11-02 /pmc/articles/PMC8563804/ /pubmed/34728724 http://dx.doi.org/10.1038/s41598-021-00966-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kawaguchi, Kohei
Takei-Hoshi, Rie
Yoshikawa, Ikue
Nishida, Keiji
Kobayashi, Makoto
Kusano, Miyako
Lu, Yu
Ariizumi, Tohru
Ezura, Hiroshi
Otagaki, Shungo
Matsumoto, Shogo
Shiratake, Katsuhiro
Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title_full Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title_fullStr Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title_full_unstemmed Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title_short Functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
title_sort functional disruption of cell wall invertase inhibitor by genome editing increases sugar content of tomato fruit without decrease fruit weight
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563804/
https://www.ncbi.nlm.nih.gov/pubmed/34728724
http://dx.doi.org/10.1038/s41598-021-00966-4
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