Modulating the strigolactone pathway to optimize tomato shoot branching for vertical farming.

IF 9.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jiwoo Lee, Myeong-Gyun Seo, Yoonseo Lim, Seungpyo Hong, Jeong-Tak An, Ho-Young Jeong, Chanhui Lee, Soon Ju Park, Giha Song, Choon-Tak Kwon
{"title":"Modulating the strigolactone pathway to optimize tomato shoot branching for vertical farming.","authors":"Jiwoo Lee, Myeong-Gyun Seo, Yoonseo Lim, Seungpyo Hong, Jeong-Tak An, Ho-Young Jeong, Chanhui Lee, Soon Ju Park, Giha Song, Choon-Tak Kwon","doi":"10.1111/jipb.70059","DOIUrl":null,"url":null,"abstract":"<p><p>Optimizing plant architecture for specific cultivation methods is essential for enhancing fruit productivity. Unlike indeterminate growth plants, the total productivity of determinate growth plants relies on cumulative fruit production and synchronized fruit ripening from both main and axillary shoots. Here, we focused on SlD14 and SlMAX1, two key genes involved in the regulation of strigolactone (SL) signaling and biosynthesis, with the goal of maximizing yield and synchronizing fruit ripening by fine-tuning axillary shoot growth. Using clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology, we found that the sld14, slmax1, and sld14 slmax1 mutant plants exhibited reduced plant height and increased axillary shoot proliferation compared to wild-type plants. However, these mutants showed reduced yield and delayed ripening, likely due to a source-sink imbalance caused by excessive axillary shoot development. A weak sld14 allele displayed a milder phenotype, maintaining total fruit yield and harvest index despite smaller individual fruit size. These findings indicate that allelic variation in SL-related genes can influence plant architecture and yield components. Our results suggest that weak or partial alleles may serve as promising targets for tailoring tomato architecture to space-limited cultivation systems.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":" ","pages":""},"PeriodicalIF":9.3000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/jipb.70059","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Optimizing plant architecture for specific cultivation methods is essential for enhancing fruit productivity. Unlike indeterminate growth plants, the total productivity of determinate growth plants relies on cumulative fruit production and synchronized fruit ripening from both main and axillary shoots. Here, we focused on SlD14 and SlMAX1, two key genes involved in the regulation of strigolactone (SL) signaling and biosynthesis, with the goal of maximizing yield and synchronizing fruit ripening by fine-tuning axillary shoot growth. Using clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology, we found that the sld14, slmax1, and sld14 slmax1 mutant plants exhibited reduced plant height and increased axillary shoot proliferation compared to wild-type plants. However, these mutants showed reduced yield and delayed ripening, likely due to a source-sink imbalance caused by excessive axillary shoot development. A weak sld14 allele displayed a milder phenotype, maintaining total fruit yield and harvest index despite smaller individual fruit size. These findings indicate that allelic variation in SL-related genes can influence plant architecture and yield components. Our results suggest that weak or partial alleles may serve as promising targets for tailoring tomato architecture to space-limited cultivation systems.

调节独角孤内酯途径优化垂直栽培番茄枝分枝。
优化特定栽培方法的植物结构对提高果实产量至关重要。与不确定生长植物不同,确定生长植物的总生产力依赖于累积的果实产量和主芽和腋芽的同步果实成熟。本研究重点研究了SlD14和SlMAX1这两个参与调节独脚金内酯信号和生物合成的关键基因,目的是通过微调腋芽生长来实现产量最大化和同步果实成熟。利用集群规则间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9 (Cas9)技术,我们发现sld14、slmax1和sld14 slmax1突变株与野生型相比,株高降低,腋芽增殖增加。然而,这些突变体表现出产量下降和成熟延迟,可能是由于腋芽发育过度导致源库不平衡。弱sld14等位基因表现出较温和的表型,尽管单果尺寸较小,但保持了果实总产量和收获指数。这些发现表明,sl相关基因的等位基因变异可以影响植物的结构和产量成分。我们的研究结果表明,弱或部分等位基因可能作为有希望的目标,以定制番茄结构,以适应空间有限的栽培系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Integrative Plant Biology
Journal of Integrative Plant Biology 生物-生化与分子生物学
CiteScore
18.00
自引率
5.30%
发文量
220
审稿时长
3 months
期刊介绍: Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信