Xueling Ye , Pan Wang , Ranfei Luo , Zhen Gan , Peiyu Yang , Wenjun Sun , Yu Fan , Changying Liu , Yan Wan , Qi Wu , Xiaoyong Wu , Dabing Xiang , Tingting Yan , Jie Kang , Liang Zou , Gang Zhao , Jianguo Wen
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Results showed that compared with their respective wild types, transpiration rate, stomatal conductance, net photosynthetic rate, and yield of effective quantum of photosystem Ⅱ were all increased in both mutants. The number of chloroplasts increased, and the number of granum lamellas was increased, and more tightly connected. These changes led to increased photosynthetic pigment contents in mutants. The unbalanced arrangement of upper and lower epidermal cells led to leaf curling in the mutants. The transcriptomic analysis detected 510 genes that were differentially expressed between both of the mutants and their respective wild types (i.e., Xi5M vs Xi5, and P10M vs PP10). They were mainly enriched in plant-pathogen interaction, plant hormone signal transduction, MAPK signaling pathway, phenylpropanoid biosynthesis, and ABC transporters. Analyses of leaf characteristics, function annotation of the differentially expressed genes (DEGs), and protein-protein interaction networks revealed 12 candidate genes which, by regulating cell development and plant hormone response, potentially regulated leaf curliness. 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引用次数: 0
摘要
鞑靼荞麦(Fagopyrum tataricum Gaertn.)为了获得高产,这种作物通常被密集种植。人们认为,叶片适度卷曲和直立有利于提高密植作物的光合效率。然而,有关该物种卷叶的研究报道很少。本文报告的研究采用细胞学、生理学和转录组学方法分析了两种叶片卷曲和直立的 EMS 突变体 Xi5M 和 P10M。结果表明,与各自的野生型相比,两个突变体的蒸腾速率、气孔导度、净光合速率和光系统Ⅱ的有效量子产量都有所增加。叶绿体数量增加,粒层数量增加,且连接更紧密。这些变化导致突变体光合色素含量增加。上下表皮细胞的不平衡排列导致突变体叶片卷曲。转录组分析检测到 510 个基因在两个突变体和各自的野生型(即 Xi5M vs Xi5 和 P10M vs PP10)之间有差异表达。这些基因主要富集在植物与病原体相互作用、植物激素信号转导、MAPK 信号通路、苯丙类生物合成和 ABC 转运体中。通过分析叶片特征、差异表达基因(DEGs)的功能注释和蛋白质-蛋白质相互作用网络,发现了12个候选基因,它们通过调控细胞发育和植物激素反应,可能调控叶片卷曲度。我们的研究开发了新的叶形材料,可通过提高群体光合效率来提高鞑靼荞麦的产量,并揭示了该物种叶片卷曲的潜在机制。
Cytological, physiological, and transcriptomic analyses reveal potential regulatory mechanisms of curly leaves in Tartary buckwheat
Tartary buckwheat (Fagopyrum tataricum Gaertn.) is a pseudocereal crop grown in sunny areas at high altitudes. To achieve high yield, this species is often densely planted. It is believed that moderately curly and upright leaves are beneficial for increasing the photosynthetic efficiency of a densely planted crop. However, little research on curly leaves has been reported for this species. The study reported here analyzed two EMS mutants Xi5M and P10M with curly and upright leaves using cytological, physiological, and transcriptomic approaches. Results showed that compared with their respective wild types, transpiration rate, stomatal conductance, net photosynthetic rate, and yield of effective quantum of photosystem Ⅱ were all increased in both mutants. The number of chloroplasts increased, and the number of granum lamellas was increased, and more tightly connected. These changes led to increased photosynthetic pigment contents in mutants. The unbalanced arrangement of upper and lower epidermal cells led to leaf curling in the mutants. The transcriptomic analysis detected 510 genes that were differentially expressed between both of the mutants and their respective wild types (i.e., Xi5M vs Xi5, and P10M vs PP10). They were mainly enriched in plant-pathogen interaction, plant hormone signal transduction, MAPK signaling pathway, phenylpropanoid biosynthesis, and ABC transporters. Analyses of leaf characteristics, function annotation of the differentially expressed genes (DEGs), and protein-protein interaction networks revealed 12 candidate genes which, by regulating cell development and plant hormone response, potentially regulated leaf curliness. Our study developed new leaf-shaped materials that could be valuable in enhancing the yield of Tartary buckwheat by improving population photosynthetic efficiency and revealed potential mechanisms of leaf curliness in this species.
期刊介绍:
Environmental and Experimental Botany (EEB) publishes research papers on the physical, chemical, biological, molecular mechanisms and processes involved in the responses of plants to their environment.
In addition to research papers, the journal includes review articles. Submission is in agreement with the Editors-in-Chief.
The Journal also publishes special issues which are built by invited guest editors and are related to the main themes of EEB.
The areas covered by the Journal include:
(1) Responses of plants to heavy metals and pollutants
(2) Plant/water interactions (salinity, drought, flooding)
(3) Responses of plants to radiations ranging from UV-B to infrared
(4) Plant/atmosphere relations (ozone, CO2 , temperature)
(5) Global change impacts on plant ecophysiology
(6) Biotic interactions involving environmental factors.