Yan Liu , Qinglin Sun , Qiguang Wang , Hao Wu , Yuting Zhang , Chunlong Li , Dong Meng , Junhong Zhang , Zaikang Tong
{"title":"揭示PbUGT73EC3参与旱情胁迫的UGT基因家族全基因组鉴定","authors":"Yan Liu , Qinglin Sun , Qiguang Wang , Hao Wu , Yuting Zhang , Chunlong Li , Dong Meng , Junhong Zhang , Zaikang Tong","doi":"10.1016/j.stress.2025.101012","DOIUrl":null,"url":null,"abstract":"<div><div>Drought stress significantly limits plant growth and development, and previous studies have demonstrated that glycosyltransferases play crucial roles in stress responses. However, the mechanisms by which <em>UGT</em> genes confer drought tolerance in <em>Phoebe bournei</em> remain largely unknown. In this study, a total of 151 <em>PbUGT</em> genes were identified and systematically named. Phylogenetic analysis classified these genes into 22 subfamilies, all of which contain the conserved PSPG box. Cis-element analysis identified a large number of stress-responsive elements in the promoters of <em>PbUGT</em> members. Combined transcriptomic and RT-qPCR analyses showed that the majority of members from the <em>UGT73, UGT74, UGT85, UGT89</em>, and <em>UGT707</em> subfamilies were highly expressed under PEG-induced drought conditions. Moreover, nine candidate genes exhibited significant transcriptional responses to drought stress. <em>PbUGT73EC3</em>, in particular, was selected for functional validation. In all three transgenic systems, its overexpression significantly increased the accumulation of kaempferol-3-<em>O</em>-rutinoside. The <em>PbUGT73EC3-</em>overexpressing lines displayed enhanced drought tolerance, with increased flavonoid content, elevated activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), and reduced levels of malondialdehyde (MDA), hydrogen peroxide (H₂O₂), and leaf water loss rate. These results suggest that <em>PbUGT73EC3</em> may enhance plant drought tolerance by regulating the biosynthesis of kaempferol-3-O-rutinoside and promoting the scavenging of reactive oxygen species (ROS) through glycosylation. In summary, these findings provide a comprehensive characterization of the <em>UGT</em> gene family in <em>P. bournei</em> and elucidate their potential roles in drought stress responses, offering a theoretical basis for molecular breeding aimed at improving drought tolerance and for further functional studies of <em>UGT</em> genes.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"18 ","pages":"Article 101012"},"PeriodicalIF":6.8000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genome-wide identification of the UGT gene family revealing PbUGT73EC3 participating in drought stress in Phoebe bournei\",\"authors\":\"Yan Liu , Qinglin Sun , Qiguang Wang , Hao Wu , Yuting Zhang , Chunlong Li , Dong Meng , Junhong Zhang , Zaikang Tong\",\"doi\":\"10.1016/j.stress.2025.101012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Drought stress significantly limits plant growth and development, and previous studies have demonstrated that glycosyltransferases play crucial roles in stress responses. However, the mechanisms by which <em>UGT</em> genes confer drought tolerance in <em>Phoebe bournei</em> remain largely unknown. In this study, a total of 151 <em>PbUGT</em> genes were identified and systematically named. Phylogenetic analysis classified these genes into 22 subfamilies, all of which contain the conserved PSPG box. Cis-element analysis identified a large number of stress-responsive elements in the promoters of <em>PbUGT</em> members. Combined transcriptomic and RT-qPCR analyses showed that the majority of members from the <em>UGT73, UGT74, UGT85, UGT89</em>, and <em>UGT707</em> subfamilies were highly expressed under PEG-induced drought conditions. Moreover, nine candidate genes exhibited significant transcriptional responses to drought stress. <em>PbUGT73EC3</em>, in particular, was selected for functional validation. In all three transgenic systems, its overexpression significantly increased the accumulation of kaempferol-3-<em>O</em>-rutinoside. The <em>PbUGT73EC3-</em>overexpressing lines displayed enhanced drought tolerance, with increased flavonoid content, elevated activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), and reduced levels of malondialdehyde (MDA), hydrogen peroxide (H₂O₂), and leaf water loss rate. These results suggest that <em>PbUGT73EC3</em> may enhance plant drought tolerance by regulating the biosynthesis of kaempferol-3-O-rutinoside and promoting the scavenging of reactive oxygen species (ROS) through glycosylation. In summary, these findings provide a comprehensive characterization of the <em>UGT</em> gene family in <em>P. bournei</em> and elucidate their potential roles in drought stress responses, offering a theoretical basis for molecular breeding aimed at improving drought tolerance and for further functional studies of <em>UGT</em> genes.</div></div>\",\"PeriodicalId\":34736,\"journal\":{\"name\":\"Plant Stress\",\"volume\":\"18 \",\"pages\":\"Article 101012\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Stress\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667064X25002805\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X25002805","RegionNum":0,"RegionCategory":null,"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
干旱胁迫严重限制了植物的生长发育,已有研究表明糖基转移酶在干旱胁迫响应中起着至关重要的作用。然而,UGT基因赋予Phoebe bournei耐旱性的机制在很大程度上仍然未知。本研究共鉴定出151个PbUGT基因并系统命名。系统发育分析将这些基因分为22个亚家族,均含有保守的PSPG盒。顺式元件分析在PbUGT成员的启动子中发现了大量的应力响应元件。转录组学和RT-qPCR联合分析显示,UGT73、UGT74、UGT85、UGT89和UGT707亚家族的大部分成员在peg诱导的干旱条件下高表达。此外,9个候选基因对干旱胁迫表现出显著的转录响应。特别是选择PbUGT73EC3进行功能验证。在三种转基因体系中,其过表达均显著增加山奈酚-3- o -芦丁苷的积累。pbugt73ec3过表达系表现出更强的抗旱性,类黄酮含量增加,超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性升高,丙二醛(MDA)、过氧化氢(h2o2)水平降低,叶片失水率降低。这些结果表明,PbUGT73EC3可能通过调节山奈酚-3- o -芦丁苷的生物合成和通过糖基化促进活性氧(ROS)的清除来增强植物的抗旱性。综上所述,这些研究结果提供了布氏假单胞菌UGT基因家族的全面特征,并阐明了其在干旱胁迫响应中的潜在作用,为旨在提高耐旱性的分子育种和进一步研究UGT基因的功能提供了理论基础。
Genome-wide identification of the UGT gene family revealing PbUGT73EC3 participating in drought stress in Phoebe bournei
Drought stress significantly limits plant growth and development, and previous studies have demonstrated that glycosyltransferases play crucial roles in stress responses. However, the mechanisms by which UGT genes confer drought tolerance in Phoebe bournei remain largely unknown. In this study, a total of 151 PbUGT genes were identified and systematically named. Phylogenetic analysis classified these genes into 22 subfamilies, all of which contain the conserved PSPG box. Cis-element analysis identified a large number of stress-responsive elements in the promoters of PbUGT members. Combined transcriptomic and RT-qPCR analyses showed that the majority of members from the UGT73, UGT74, UGT85, UGT89, and UGT707 subfamilies were highly expressed under PEG-induced drought conditions. Moreover, nine candidate genes exhibited significant transcriptional responses to drought stress. PbUGT73EC3, in particular, was selected for functional validation. In all three transgenic systems, its overexpression significantly increased the accumulation of kaempferol-3-O-rutinoside. The PbUGT73EC3-overexpressing lines displayed enhanced drought tolerance, with increased flavonoid content, elevated activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), and reduced levels of malondialdehyde (MDA), hydrogen peroxide (H₂O₂), and leaf water loss rate. These results suggest that PbUGT73EC3 may enhance plant drought tolerance by regulating the biosynthesis of kaempferol-3-O-rutinoside and promoting the scavenging of reactive oxygen species (ROS) through glycosylation. In summary, these findings provide a comprehensive characterization of the UGT gene family in P. bournei and elucidate their potential roles in drought stress responses, offering a theoretical basis for molecular breeding aimed at improving drought tolerance and for further functional studies of UGT genes.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.