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Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes

All-flesh tomato cultivars are devoid of locular gel and exhibit enhanced firmness and improved postharvest storage. Here, we show that SlMBP3 is a master regulator of locular tissue in tomato fruit and that a deletion at the gene locus underpins the All-flesh trait. Intriguingly, All-flesh varietie...

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Autores principales: Huang, Baowen, Hu, Guojian, Wang, Keke, Frasse, Pierre, Maza, Elie, Djari, Anis, Deng, Wei, Pirrello, Julien, Burlat, Vincent, Pons, Clara, Granell, Antonio, Li, Zhengguo, van der Rest, Benoît, Bouzayen, Mondher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616914/
https://www.ncbi.nlm.nih.gov/pubmed/34824241
http://dx.doi.org/10.1038/s41467-021-27117-7
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author Huang, Baowen
Hu, Guojian
Wang, Keke
Frasse, Pierre
Maza, Elie
Djari, Anis
Deng, Wei
Pirrello, Julien
Burlat, Vincent
Pons, Clara
Granell, Antonio
Li, Zhengguo
van der Rest, Benoît
Bouzayen, Mondher
author_facet Huang, Baowen
Hu, Guojian
Wang, Keke
Frasse, Pierre
Maza, Elie
Djari, Anis
Deng, Wei
Pirrello, Julien
Burlat, Vincent
Pons, Clara
Granell, Antonio
Li, Zhengguo
van der Rest, Benoît
Bouzayen, Mondher
author_sort Huang, Baowen
collection PubMed
description All-flesh tomato cultivars are devoid of locular gel and exhibit enhanced firmness and improved postharvest storage. Here, we show that SlMBP3 is a master regulator of locular tissue in tomato fruit and that a deletion at the gene locus underpins the All-flesh trait. Intriguingly, All-flesh varieties lack the deleterious phenotypes reported previously for SlMBP3 under-expressing lines and which preclude any potential commercial use. We resolve the causal factor for this phenotypic divergence through the discovery of a natural mutation at the SlAGL11 locus, a close homolog of SlMBP3. Misexpressing SlMBP3 impairs locular gel formation through massive transcriptomic reprogramming at initial phases of fruit development. SlMBP3 influences locule gel formation by controlling cell cycle and cell expansion genes, indicating that important components of fruit softening are determined at early pre-ripening stages. Our findings define potential breeding targets for improved texture in tomato and possibly other fleshy fruits.
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spelling pubmed-86169142021-12-01 Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes Huang, Baowen Hu, Guojian Wang, Keke Frasse, Pierre Maza, Elie Djari, Anis Deng, Wei Pirrello, Julien Burlat, Vincent Pons, Clara Granell, Antonio Li, Zhengguo van der Rest, Benoît Bouzayen, Mondher Nat Commun Article All-flesh tomato cultivars are devoid of locular gel and exhibit enhanced firmness and improved postharvest storage. Here, we show that SlMBP3 is a master regulator of locular tissue in tomato fruit and that a deletion at the gene locus underpins the All-flesh trait. Intriguingly, All-flesh varieties lack the deleterious phenotypes reported previously for SlMBP3 under-expressing lines and which preclude any potential commercial use. We resolve the causal factor for this phenotypic divergence through the discovery of a natural mutation at the SlAGL11 locus, a close homolog of SlMBP3. Misexpressing SlMBP3 impairs locular gel formation through massive transcriptomic reprogramming at initial phases of fruit development. SlMBP3 influences locule gel formation by controlling cell cycle and cell expansion genes, indicating that important components of fruit softening are determined at early pre-ripening stages. Our findings define potential breeding targets for improved texture in tomato and possibly other fleshy fruits. Nature Publishing Group UK 2021-11-25 /pmc/articles/PMC8616914/ /pubmed/34824241 http://dx.doi.org/10.1038/s41467-021-27117-7 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Baowen
Hu, Guojian
Wang, Keke
Frasse, Pierre
Maza, Elie
Djari, Anis
Deng, Wei
Pirrello, Julien
Burlat, Vincent
Pons, Clara
Granell, Antonio
Li, Zhengguo
van der Rest, Benoît
Bouzayen, Mondher
Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title_full Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title_fullStr Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title_full_unstemmed Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title_short Interaction of two MADS-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
title_sort interaction of two mads-box genes leads to growth phenotype divergence of all-flesh type of tomatoes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616914/
https://www.ncbi.nlm.nih.gov/pubmed/34824241
http://dx.doi.org/10.1038/s41467-021-27117-7
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