Gaston A Pizzio, Cristian Mayordomo, Jonatan Illescas-Miranda, Alberto Coego, Mar Bono, Mayra Sanchez-Olvera, Constanza Martin-Vasquez, Kajal Samantara, Ebe Merilo, Javier Forment, Juan Carlos Estevez, Sergio G Nebauer, Pedro L Rodriguez
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We have generated a pentuple pyl mutant in the allotetraploid Nicotiana benthamiana through CRISPR/Cas9 gene editing. The pentuple mutant is impaired in 2 NbPYL1-like and 3 NbPYL8-like receptors, affecting the regulation of transpiration and several ABA-dependent transcriptional processes. RNA-seq and metabolite analysis revealed that the synthesis of galactinol, an essential precursor for the osmoprotective raffinose family of oligosaccharides, is ABA-dependent and impaired in the mutant under osmotic stress. In contrast, our results show that, under well-watered conditions, partial inactivation of ABA signaling leads to higher CO<sub>2</sub> entry and photosynthesis in the mutant than in WT. Photosynthesis analyses revealed an increased CO<sub>2</sub> diffusion capacity mediated by higher stomatal and mesophyll conductances, and higher substomatal CO<sub>2</sub> concentration in the pentuple mutant. RNA-seq analyses revealed that genes associated with cell wall loosening (e.g., expansins) and porosity were strongly downregulated by ABA in WT. 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引用次数: 0
摘要
用于光合作用的二氧化碳输入与蒸腾失水之间的平衡对植物生长至关重要,而 ABA 信号可影响这种平衡。为了测试 ABA 如何平衡植物生长和环境适应,我们在水分充足或干旱条件下对生物技术作物烟草本甘蓝(Nicotiana benthamiana)进行了分子遗传学研究。由于PYR/PYL/RCAR ABA受体家族的多基因性质及其功能冗余,作物中的ABA信号研究变得复杂,这在多倍体植物中尤其具有挑战性。我们通过 CRISPR/Cas9 基因编辑技术在异源四倍体烟草(Nicotiana benthamiana)中产生了一个五倍体 pyl 突变体。该五倍体突变体的 2 个 NbPYL1 样受体和 3 个 NbPYL8 样受体受损,影响了蒸腾作用和多个 ABA 依赖性转录过程的调控。RNA-seq 和代谢物分析表明,半乳糖苷(具有渗透保护作用的棉子糖系列低聚糖的重要前体)的合成依赖于 ABA,在渗透胁迫下,突变体的半乳糖苷合成受损。相反,我们的结果表明,在水分充足的条件下,ABA 信号的部分失活导致突变体的二氧化碳进入量和光合作用高于 WT。光合作用分析表明,五倍体突变体通过提高气孔和叶肉间传导以及提高气孔下CO2浓度,提高了CO2扩散能力。RNA-seq 分析显示,与细胞壁松弛(如扩张素)和多孔性相关的基因在 WT 中受到 ABA 的强烈下调。总之,当水分不受限制时,由 ABA 受体介导的 ABA 对蒸腾作用控制的部分缓解会对光合作用产生积极影响,但代价是水分利用效率降低。
Basal ABA signaling balances transpiration and photosynthesis.
The balance between the CO2 entry for photosynthesis and transpiration water loss is crucial for plant growth, and ABA signaling can affect this equilibrium. To test how ABA balances plant growth and environmental adaptation, we performed molecular genetics studies in the biotech crop Nicotiana benthamiana under well-watered or drought conditions. Studies on ABA signaling in crops are complicated by the multigenic nature of the PYR/PYL/RCAR ABA receptor family and its functional redundancy, which is particularly challenging in polyploid plants. We have generated a pentuple pyl mutant in the allotetraploid Nicotiana benthamiana through CRISPR/Cas9 gene editing. The pentuple mutant is impaired in 2 NbPYL1-like and 3 NbPYL8-like receptors, affecting the regulation of transpiration and several ABA-dependent transcriptional processes. RNA-seq and metabolite analysis revealed that the synthesis of galactinol, an essential precursor for the osmoprotective raffinose family of oligosaccharides, is ABA-dependent and impaired in the mutant under osmotic stress. In contrast, our results show that, under well-watered conditions, partial inactivation of ABA signaling leads to higher CO2 entry and photosynthesis in the mutant than in WT. Photosynthesis analyses revealed an increased CO2 diffusion capacity mediated by higher stomatal and mesophyll conductances, and higher substomatal CO2 concentration in the pentuple mutant. RNA-seq analyses revealed that genes associated with cell wall loosening (e.g., expansins) and porosity were strongly downregulated by ABA in WT. In summary, a partial relief of the ABA control on transpiration mediated by ABA receptors positively affects photosynthesis when water is not limited, at the expense of reduced water use efficiency.
期刊介绍:
Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.