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Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape

Fruit shape is an important trait that attracts consumers, and the regulation of genes related to cell division is crucial for shaping multicellular organs. In Arabidopsis, MYB3R transcription factors, which harbor three imperfect repeats in the N-terminus, control organ growth by regulating cell di...

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Autores principales: Zheng, Qingyou, Takei-Hoshi, Rie, Okumura, Hitomi, Ito, Masaki, Kawaguchi, Kohei, Otagaki, Shungo, Matsumoto, Shogo, Luo, Zhengrong, Zhang, Qinglin, Shiratake, Katsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730800/
https://www.ncbi.nlm.nih.gov/pubmed/36070755
http://dx.doi.org/10.1093/jxb/erac352
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author Zheng, Qingyou
Takei-Hoshi, Rie
Okumura, Hitomi
Ito, Masaki
Kawaguchi, Kohei
Otagaki, Shungo
Matsumoto, Shogo
Luo, Zhengrong
Zhang, Qinglin
Shiratake, Katsuhiro
author_facet Zheng, Qingyou
Takei-Hoshi, Rie
Okumura, Hitomi
Ito, Masaki
Kawaguchi, Kohei
Otagaki, Shungo
Matsumoto, Shogo
Luo, Zhengrong
Zhang, Qinglin
Shiratake, Katsuhiro
author_sort Zheng, Qingyou
collection PubMed
description Fruit shape is an important trait that attracts consumers, and the regulation of genes related to cell division is crucial for shaping multicellular organs. In Arabidopsis, MYB3R transcription factors, which harbor three imperfect repeats in the N-terminus, control organ growth by regulating cell division. However, the function of MYB3Rs in tomato remains unknown. Here, we characterized tomato SlMYB3R3, which was preferentially expressed in flowers and placed in a subclade with two Arabidopsis cell cycle suppressors (MYB3R3/5). slmyb3r3 knockout mutants were generated using the CRISPR/Cas9 system. Morphological observation of the slmyb3r3 mutants showed that fruits that were elongated and occasionally peanut-like in shape were formed, which was caused by significantly increased cell numbers in the longitudinal direction. Transcriptome and yeast one-hybrid assay results suggested that SlMYB3R3 acted as a suppressor of cell-cycle-related genes by binding to the mitosis-specific activator (MSA) motifs in their promoters. Taken together, knock out of the suppressor SlMYB3R3 leads to elongated fruit, which results from the altered cell division pattern at the ovary stage, by regulating cell-cycle-related genes in an MSA-dependent manner. Our results suggest that SlMYB3R3 and its orthologs have the potential to change fruit shape as part of the molecular breeding of fruit crops.
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spelling pubmed-97308002022-12-13 Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape Zheng, Qingyou Takei-Hoshi, Rie Okumura, Hitomi Ito, Masaki Kawaguchi, Kohei Otagaki, Shungo Matsumoto, Shogo Luo, Zhengrong Zhang, Qinglin Shiratake, Katsuhiro J Exp Bot Research Papers Fruit shape is an important trait that attracts consumers, and the regulation of genes related to cell division is crucial for shaping multicellular organs. In Arabidopsis, MYB3R transcription factors, which harbor three imperfect repeats in the N-terminus, control organ growth by regulating cell division. However, the function of MYB3Rs in tomato remains unknown. Here, we characterized tomato SlMYB3R3, which was preferentially expressed in flowers and placed in a subclade with two Arabidopsis cell cycle suppressors (MYB3R3/5). slmyb3r3 knockout mutants were generated using the CRISPR/Cas9 system. Morphological observation of the slmyb3r3 mutants showed that fruits that were elongated and occasionally peanut-like in shape were formed, which was caused by significantly increased cell numbers in the longitudinal direction. Transcriptome and yeast one-hybrid assay results suggested that SlMYB3R3 acted as a suppressor of cell-cycle-related genes by binding to the mitosis-specific activator (MSA) motifs in their promoters. Taken together, knock out of the suppressor SlMYB3R3 leads to elongated fruit, which results from the altered cell division pattern at the ovary stage, by regulating cell-cycle-related genes in an MSA-dependent manner. Our results suggest that SlMYB3R3 and its orthologs have the potential to change fruit shape as part of the molecular breeding of fruit crops. Oxford University Press 2022-09-07 /pmc/articles/PMC9730800/ /pubmed/36070755 http://dx.doi.org/10.1093/jxb/erac352 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Zheng, Qingyou
Takei-Hoshi, Rie
Okumura, Hitomi
Ito, Masaki
Kawaguchi, Kohei
Otagaki, Shungo
Matsumoto, Shogo
Luo, Zhengrong
Zhang, Qinglin
Shiratake, Katsuhiro
Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title_full Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title_fullStr Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title_full_unstemmed Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title_short Genome editing of SlMYB3R3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
title_sort genome editing of slmyb3r3, a cell cycle transcription factor gene of tomato, induces elongated fruit shape
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730800/
https://www.ncbi.nlm.nih.gov/pubmed/36070755
http://dx.doi.org/10.1093/jxb/erac352
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