ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness

Malic acid markedly affects watermelon flavor. Reducing the malic acid content can significantly increase the sweetness of watermelon. An effective solution strategy is to reduce watermelon malic acid content through molecular breeding technology. In this study, we measured the TSS and pH of six wat...

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Main Authors: Congji Yang, Jiale Shi, Yuanyuan Qin, ShengQi Hua, Jiancheng Bao, Xueyan Liu, Yuqi Peng, Yige Gu, Wei Dong
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:GM Crops & Food
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Online Access:https://www.tandfonline.com/doi/10.1080/21645698.2025.2452702
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author Congji Yang
Jiale Shi
Yuanyuan Qin
ShengQi Hua
Jiancheng Bao
Xueyan Liu
Yuqi Peng
Yige Gu
Wei Dong
author_facet Congji Yang
Jiale Shi
Yuanyuan Qin
ShengQi Hua
Jiancheng Bao
Xueyan Liu
Yuqi Peng
Yige Gu
Wei Dong
author_sort Congji Yang
collection DOAJ
description Malic acid markedly affects watermelon flavor. Reducing the malic acid content can significantly increase the sweetness of watermelon. An effective solution strategy is to reduce watermelon malic acid content through molecular breeding technology. In this study, we measured the TSS and pH of six watermelon varieties at four growth nodes. The TSS content was very low at 10 DAP and accumulated rapidly at 18, 26, and 34 DAP. Three phosphoenolpyruvate carboxykinase (PEPCK) genes of watermelon were identified and analyzed. The ClaPEPCK4 expression was inversely proportional to malate content variations in fruits. In transgenic watermelon plants, overexpressing the ClaPEPCK4 gene, malic acid content markedly decreased. In the knockout transgenic watermelon plants, two SNP mutations and one base deletion occurred in the ClaPEPCK4 gene, with the malic acid content in the leaves increasing considerably and the PEPCK enzyme activity reduced to half of the wild-type. It is interesting that the ClaPEPCK4 gene triggered the closure of leaf stomata under dark conditions in the knockout transgenic plants, which indicated its involvement in stomatal movement. In conclusion, this study provides a gene target ClaPEPCK4 for creating innovative new high-sweetness watermelon varieties.
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institution Kabale University
issn 2164-5698
2164-5701
language English
publishDate 2025-12-01
publisher Taylor & Francis Group
record_format Article
series GM Crops & Food
spelling doaj-art-d4d45b4a4ea943769591bb27776f07c62025-01-14T16:38:16ZengTaylor & Francis GroupGM Crops & Food2164-56982164-57012025-12-0116115617010.1080/21645698.2025.2452702ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetnessCongji Yang0Jiale Shi1Yuanyuan Qin2ShengQi Hua3Jiancheng Bao4Xueyan Liu5Yuqi Peng6Yige Gu7Wei Dong8State Key Laboratory of Cotton Biology, School of Life Sciences, Henan University, Kaifeng, ChinaState Key Laboratory of Cotton Biology, School of Life Sciences, Henan University, Kaifeng, ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaSchool of Life Science, Henan University, Kaifeng, Henan, People’s Republic of ChinaMalic acid markedly affects watermelon flavor. Reducing the malic acid content can significantly increase the sweetness of watermelon. An effective solution strategy is to reduce watermelon malic acid content through molecular breeding technology. In this study, we measured the TSS and pH of six watermelon varieties at four growth nodes. The TSS content was very low at 10 DAP and accumulated rapidly at 18, 26, and 34 DAP. Three phosphoenolpyruvate carboxykinase (PEPCK) genes of watermelon were identified and analyzed. The ClaPEPCK4 expression was inversely proportional to malate content variations in fruits. In transgenic watermelon plants, overexpressing the ClaPEPCK4 gene, malic acid content markedly decreased. In the knockout transgenic watermelon plants, two SNP mutations and one base deletion occurred in the ClaPEPCK4 gene, with the malic acid content in the leaves increasing considerably and the PEPCK enzyme activity reduced to half of the wild-type. It is interesting that the ClaPEPCK4 gene triggered the closure of leaf stomata under dark conditions in the knockout transgenic plants, which indicated its involvement in stomatal movement. In conclusion, this study provides a gene target ClaPEPCK4 for creating innovative new high-sweetness watermelon varieties.https://www.tandfonline.com/doi/10.1080/21645698.2025.2452702Fruit developmentgluconeogenesismalic acidPEPCKwatermelon
spellingShingle Congji Yang
Jiale Shi
Yuanyuan Qin
ShengQi Hua
Jiancheng Bao
Xueyan Liu
Yuqi Peng
Yige Gu
Wei Dong
ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
GM Crops & Food
Fruit development
gluconeogenesis
malic acid
PEPCK
watermelon
title ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
title_full ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
title_fullStr ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
title_full_unstemmed ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
title_short ClaPEPCK4: target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
title_sort clapepck4 target gene for breeding innovative watermelon germplasm with low malic acid and high sweetness
topic Fruit development
gluconeogenesis
malic acid
PEPCK
watermelon
url https://www.tandfonline.com/doi/10.1080/21645698.2025.2452702
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