Pulled GA signal orchestration proteome reconfiguration and redundancy cycling via PtGA2ox10-mediated metabolic gatekeeping in Chinese pine seeds.

IF 4.5 2区 生物学 Q1 PLANT SCIENCES
Xinxiu Zuo, Shuai Liu, Yanjun Li, Yanyan Zhang, Duxian Lu, Shihui Niu, Xiaojuan Li, Jinxing Lin, Yaning Cui
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引用次数: 0

Abstract

Key message: This study reveals the molecular mechanisms of seed dormancy and germination in Chinese pine, highlighting the key roles of GA and ABA pathways and specific genes in regulating germination, growth, and stress resistance. Chinese pine (Pinus tabuliformis) is an ecologically and economically vital conifer species in China, serving critical functions in forest regeneration, soil conservation, and carbon sequestration. Despite its ecological importance, the molecular mechanisms governing seed dormancy release and germination in this species remain poorly understood. Using an integrative approach that combines advanced microscopy, hormone profiling, metabolomics, and whole transcriptome sequencing, we uncovered novel molecular insights into these crucial developmental processes. Optical and transmission electron microscopy revealed that protein bodies aggregated in aleurone cells during dormancy release. High-performance liquid chromatography-mass spectrometry (HPLC-MS) analysis revealed distinct hormonal antagonism: gibberellin (GA) levels peaked during dormancy release (S2), with GA3 increased by 8.1-fold (from 41.37 ± 8.68 ng/g to 336.97 ± 106.14 ng/g), whereas abscisic acid (ABA) decreased by 63.6% (from 54.39 ± 1.83 ng/g at S1 to 19.80 ± 0.73 ng/g at S3), which negatively correlated with seed germination. Moreover, these hormonal changes were accompanied by profound metabolic reprogramming, which included a 6.0-fold increase in fructose content and a 12.3-fold increase in glucose content, whereas sucrose levels decreased by 48.1%, indicating enhanced carbohydrate mobilization during the germination phase (S3). Importantly, our transcriptomic analyses identified three novel regulatory genes (PtGA2ox10, PtRGA1, and PtABI2) with distinct expression patterns and functional roles during dormancy-germination transitions. Most significantly, we provide the first experimental evidence that PtGA2ox10 plays a dual regulatory role in both germination control and stress response pathways, a previously unrecognized function in conifers. These findings fundamentally advance our understanding of pine seed biology and establish new research directions in conifer molecular physiology.

通过ptga2ox10介导的代谢守门,拉式GA信号协调蛋白质组重构和冗余循环
本研究揭示了油松种子休眠和萌发的分子机制,重点揭示了GA和ABA通路以及特定基因在调控油松种子萌发、生长和抗逆性中的关键作用。油松(Pinus tabuliformis)是中国具有重要生态和经济价值的针叶林树种,在森林更新、土壤保持和固碳等方面具有重要作用。尽管其具有重要的生态意义,但控制该物种种子休眠释放和发芽的分子机制仍然知之甚少。利用结合先进显微镜、激素谱、代谢组学和全转录组测序的综合方法,我们发现了这些关键发育过程的新分子见解。光学和透射电镜显示,在休眠释放过程中,蛋白体聚集在糊粉细胞中。高效液相色谱-质谱(HPLC-MS)分析显示出明显的激素拮抗作用:赤霉素(GA)水平在休眠释放(S2)期间达到峰值,GA3含量增加8.1倍(从41.37±8.68 ng/g增加到336.97±106.14 ng/g),而脱落酸(ABA)含量减少63.6%(从S1的54.39±1.83 ng/g增加到S3的19.80±0.73 ng/g),与种子萌发呈负相关。此外,这些激素变化伴随着深刻的代谢重编程,其中果糖含量增加了6.0倍,葡萄糖含量增加了12.3倍,而蔗糖水平下降了48.1%,表明萌发期碳水化合物动员增强(S3)。重要的是,我们的转录组学分析确定了三个新的调控基因(PtGA2ox10、PtRGA1和PtABI2),它们在休眠-萌发转变过程中具有不同的表达模式和功能作用。最重要的是,我们提供了第一个实验证据,证明PtGA2ox10在发芽控制和胁迫反应途径中发挥双重调节作用,这是以前未被认识到的针叶树功能。这些发现从根本上促进了我们对松树种子生物学的认识,并为针叶树分子生理学的研究开辟了新的方向。
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
Plant Cell Reports
Plant Cell Reports 生物-植物科学
CiteScore
10.80
自引率
1.60%
发文量
135
审稿时长
3.2 months
期刊介绍: Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as: - genomics and genetics - metabolism - cell biology - abiotic and biotic stress - phytopathology - gene transfer and expression - molecular pharming - systems biology - nanobiotechnology - genome editing - phenomics and synthetic biology The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.
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