过表达表皮图案因子1的小麦气孔密度降低对红蓝光响应的影响存在差异

IF 6.9 1区 生物学 Q1 PLANT SCIENCES
Mengjie Fan, Delfi Dorussen, Hussein Gherli, Tracy Lawson
{"title":"过表达表皮图案因子1的小麦气孔密度降低对红蓝光响应的影响存在差异","authors":"Mengjie Fan, Delfi Dorussen, Hussein Gherli, Tracy Lawson","doi":"10.1093/plphys/kiaf379","DOIUrl":null,"url":null,"abstract":"Stomatal pores govern the tradeoff between CO₂ assimilation and water loss, and optimizing their performance is critical for crop resilience, particularly under dynamic field environments. Here, we show that overexpression of Triticum aestivum EPIDERMAL PATTERNING FACTOR1 (TaEPF1) in bread wheat (Triticum aestivum) reduces leaf stomatal density in a leaf surface-specific manner, with a greater decline on the abaxial surface than on the adaxial surface. TaEPF1 overexpressors exhibited substantially lower stomatal conductance than wild-type (WT) control plants, which resulted in diffusional constraints limiting photosynthesis when measured under monochromatic red light. However, upon partial substitution of red light with blue light, EPF1 overexpressors displayed an amplified and rapid stomatal opening response, particularly on the abaxial surface, where relative conductance increased by up to 90% versus 49% observed in the WT. Despite anatomical limitations in maximum conductance rate, this blue light sensitivity effectively compensated for the lower baseline gas exchange. The enhanced sensitivity to blue light was also concomitant with lower intercellular CO₂ levels under red light. When gsw responses were normalized relative to stomatal density, , stomatal sensitivity to red light was reduced at the pore level, whilst blue light sensitivity increased, which was particularly evident during abaxial surface illumination. Finally, the transgenic lines maintained a 15–20% higher water use efficiency across light regimes. These findings show a compensatory mechanism where genetically induced reduction in stomatal density is offset by heightened blue light sensitivity.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"24 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reduced stomatal density in wheat overexpressing EPIDERMAL PATTERNING FACTOR1 differentially affects red and blue light responses\",\"authors\":\"Mengjie Fan, Delfi Dorussen, Hussein Gherli, Tracy Lawson\",\"doi\":\"10.1093/plphys/kiaf379\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Stomatal pores govern the tradeoff between CO₂ assimilation and water loss, and optimizing their performance is critical for crop resilience, particularly under dynamic field environments. Here, we show that overexpression of Triticum aestivum EPIDERMAL PATTERNING FACTOR1 (TaEPF1) in bread wheat (Triticum aestivum) reduces leaf stomatal density in a leaf surface-specific manner, with a greater decline on the abaxial surface than on the adaxial surface. TaEPF1 overexpressors exhibited substantially lower stomatal conductance than wild-type (WT) control plants, which resulted in diffusional constraints limiting photosynthesis when measured under monochromatic red light. However, upon partial substitution of red light with blue light, EPF1 overexpressors displayed an amplified and rapid stomatal opening response, particularly on the abaxial surface, where relative conductance increased by up to 90% versus 49% observed in the WT. Despite anatomical limitations in maximum conductance rate, this blue light sensitivity effectively compensated for the lower baseline gas exchange. The enhanced sensitivity to blue light was also concomitant with lower intercellular CO₂ levels under red light. When gsw responses were normalized relative to stomatal density, , stomatal sensitivity to red light was reduced at the pore level, whilst blue light sensitivity increased, which was particularly evident during abaxial surface illumination. Finally, the transgenic lines maintained a 15–20% higher water use efficiency across light regimes. These findings show a compensatory mechanism where genetically induced reduction in stomatal density is offset by heightened blue light sensitivity.\",\"PeriodicalId\":20101,\"journal\":{\"name\":\"Plant Physiology\",\"volume\":\"24 1\",\"pages\":\"\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/plphys/kiaf379\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf379","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

气孔控制着二氧化碳同化和水分流失之间的平衡,优化气孔性能对作物的抗逆性至关重要,尤其是在动态田间环境下。本研究表明,面包小麦(Triticum aestivum)表皮图案因子1 (TaEPF1)的过表达以叶片表面特异性的方式降低叶片气孔密度,且叶片背面气孔密度的下降幅度大于叶片正面气孔密度的下降幅度。在单色红光下,TaEPF1过表达体的气孔导度明显低于野生型(WT)对照植物,这导致了扩散约束限制了光合作用。然而,当红光部分替换为蓝光时,EPF1过表达者表现出放大和快速的气孔打开响应,特别是在背面,相对电导增加了高达90%,而在WT中观察到的为49%。尽管最大电导率在解剖学上存在局限性,但这种蓝光敏感性有效地补偿了较低的基线气体交换。在红光下,细胞间CO₂浓度降低,对蓝光的敏感性也随之增强。当gsw响应相对于气孔密度进行归一化处理时,气孔对红光的敏感性在孔水平上降低,而对蓝光的敏感性则增加,这在背表面光照下尤为明显。最后,转基因品系在不同光照条件下保持了15-20%的高水分利用效率。这些发现显示了一种补偿机制,其中遗传诱导的气孔密度减少被蓝光敏感性的提高所抵消。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced stomatal density in wheat overexpressing EPIDERMAL PATTERNING FACTOR1 differentially affects red and blue light responses
Stomatal pores govern the tradeoff between CO₂ assimilation and water loss, and optimizing their performance is critical for crop resilience, particularly under dynamic field environments. Here, we show that overexpression of Triticum aestivum EPIDERMAL PATTERNING FACTOR1 (TaEPF1) in bread wheat (Triticum aestivum) reduces leaf stomatal density in a leaf surface-specific manner, with a greater decline on the abaxial surface than on the adaxial surface. TaEPF1 overexpressors exhibited substantially lower stomatal conductance than wild-type (WT) control plants, which resulted in diffusional constraints limiting photosynthesis when measured under monochromatic red light. However, upon partial substitution of red light with blue light, EPF1 overexpressors displayed an amplified and rapid stomatal opening response, particularly on the abaxial surface, where relative conductance increased by up to 90% versus 49% observed in the WT. Despite anatomical limitations in maximum conductance rate, this blue light sensitivity effectively compensated for the lower baseline gas exchange. The enhanced sensitivity to blue light was also concomitant with lower intercellular CO₂ levels under red light. When gsw responses were normalized relative to stomatal density, , stomatal sensitivity to red light was reduced at the pore level, whilst blue light sensitivity increased, which was particularly evident during abaxial surface illumination. Finally, the transgenic lines maintained a 15–20% higher water use efficiency across light regimes. These findings show a compensatory mechanism where genetically induced reduction in stomatal density is offset by heightened blue light sensitivity.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
×
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