PpSPL1 and PpSPL15 inhibit peach branching by increasing strigolactone synthesis.

IF 3.6 3区 生物学 Q1 PLANT SCIENCES
Planta Pub Date : 2025-03-05 DOI:10.1007/s00425-025-04659-4
Wan Pei, Jie Zhang, Ruixian Shen, Hefang Xie, Yajia Zhang, Junjie Zhang, Xiaodong Lian, Haipeng Zhang, Nan Hou, Lei Wang, Xianbo Zheng, Jun Cheng, Wei Wang, Xia Ye, Jidong Li, Xiaobei Wang, Jiancan Feng, Bin Tan
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引用次数: 0

Abstract

Main conclusion: PpSPL1 and PpSPL15 inhibit peach branching by directly binding to and upregulating the expression of strigolactone (SL) synthesis gene PpLBO1. Branch number is a crucial agronomic trait that influences tree architecture, directly affecting fruit yield and quality. It remains unknown whether SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL), an important transcription factor in determining plant architecture, is involved in the peach branching process. In this study, we found that PpSPL1 and PpSPL15 exhibited significantly higher expression levels in pillar type peach 'Sahonglongzhu' (with fewer secondary branches) compared to standard-type peach 'Okubo' (with more secondary branches). PpSPL1 and PpSPL15 can directly bind to the promoter of the SL synthesis gene PpLBO1. Transient overexpression of PpSPL1 and PpSPL15 in 'Sahonglongzhu' peach axillary buds significantly increased the expression of PpLBO1 and endogenous SL content. Conversely, opposite results were obtained when the expression of PpSPL1 and PpSPL15 was transiently silenced in peach axillary buds. Gene function analysis indicated that transient overexpression of PpSPL1 and PpSPL15 in peach seedlings clearly inhibited peach branching. On the contrary, the number of branches dramatically increased when the expression of PpSPL1 and PpSPL15 were transiently silenced in peach seedlings. These results suggested that PpSPL1 and PpSPL15 could bind to and enhance the expression of PpLBO1, further inhibiting peach branching.

PpSPL1和PpSPL15通过增加独脚金内酯合成抑制桃树分枝。
主要结论:PpSPL1和PpSPL15通过直接结合并上调独角麦内酯合成基因PpLBO1的表达抑制桃树分枝。枝数是影响树型的重要农艺性状,直接影响果实的产量和品质。SQUAMOSA启动子结合蛋白样(SPL)是决定植物结构的重要转录因子,其是否参与桃的分枝过程尚不清楚。本研究发现PpSPL1和PpSPL15在次生枝较少的柱型桃‘沙红龙珠’中的表达量显著高于次生枝较多的标准型桃‘大久保’。PpSPL1和PpSPL15可以直接结合SL合成基因PpLBO1的启动子。瞬时过表达PpSPL1和PpSPL15可显著提高‘沙红龙珠’桃腋芽中PpLBO1的表达量和内源SL含量。相反,当PpSPL1和PpSPL15在桃腋芽中短暂沉默时,得到相反的结果。基因功能分析表明,PpSPL1和PpSPL15在桃幼苗中瞬时过表达可明显抑制桃的分枝。相反,当PpSPL1和PpSPL15的表达在桃幼苗中短暂沉默时,枝数急剧增加。这些结果表明PpSPL1和PpSPL15可以结合并增强PpLBO1的表达,进一步抑制桃树的分枝。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Planta
Planta 生物-植物科学
CiteScore
7.20
自引率
2.30%
发文量
217
审稿时长
2.3 months
期刊介绍: Planta publishes timely and substantial articles on all aspects of plant biology. We welcome original research papers on any plant species. Areas of interest include biochemistry, bioenergy, biotechnology, cell biology, development, ecological and environmental physiology, growth, metabolism, morphogenesis, molecular biology, new methods, physiology, plant-microbe interactions, structural biology, and systems biology.
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