Kaituo Wang , Fei Xiang , Qinhong Liao , Jiahao Li , Changyi Lei , Yijia Xia , Chunhong Li
{"title":"TCP7在介导rbh诱导的葡萄采后果实真菌抗性中的关键作用","authors":"Kaituo Wang , Fei Xiang , Qinhong Liao , Jiahao Li , Changyi Lei , Yijia Xia , Chunhong Li","doi":"10.1016/j.plaphy.2025.110026","DOIUrl":null,"url":null,"abstract":"<div><div>(R)-β-homoserine (RBH) is a structural analogue of β-aminobutyric acid (BABA) that can enhance plant resistance to a wide range of pathogens. Here, we investigated the regulatory role of <em>VvTCP7</em> on the RBH-induced priming response against <em>Botrytis cinerea</em> in grapes. The results showed that RBH primed a defense mechanism in grape berries and enhanced their response to fungal infection. RBH upregulated the expression of a group of genes involved in SA synthesis, thus inducing SA accumulation in grapes. <em>VvTCP7</em> has high homology to <em>AtCHE</em> in Arabidopsis <em>thaliana</em> and is recognized to be a nucleus-localized protein that promotes SA synthesis. Notably, RBH elevated <em>VvTCP7</em> expression in harvested grape berries, which was accompanied by enhanced expression of <em>VvNPR1</em>, a master regulator of SAR, as well as the SA-responsive <em>PR</em> genes. Additionally, Y1H, EMSA and DLR assays confirmed that VvTCP7 has the ability to bind directly to the GGNCCC motif within the <em>VvICS</em> promoter to induce <em>VvICS</em> transcription and SA synthesis. Overexpression of VvTCP7 in Arabidopsis led to a marked increase in the transcription of <em>PR</em> genes, enhancing defensive response to <em>B. cinerea</em>. However, the VvTCP7 knockout led to a decrease in <em>PR</em> gene expression and increased susceptibility to the fungus. Collectively, the data suggest that VvTCP7 contributes to RBH-induced SAR priming by activating the SA synthesis and resultant enhances SAR defenses to combat fungal invasion.</div></div>","PeriodicalId":20234,"journal":{"name":"Plant Physiology and Biochemistry","volume":"225 ","pages":"Article 110026"},"PeriodicalIF":6.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Critical role of TCP7 in mediating RBH-induced fungal resistance in postharvest grape berries\",\"authors\":\"Kaituo Wang , Fei Xiang , Qinhong Liao , Jiahao Li , Changyi Lei , Yijia Xia , Chunhong Li\",\"doi\":\"10.1016/j.plaphy.2025.110026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>(R)-β-homoserine (RBH) is a structural analogue of β-aminobutyric acid (BABA) that can enhance plant resistance to a wide range of pathogens. Here, we investigated the regulatory role of <em>VvTCP7</em> on the RBH-induced priming response against <em>Botrytis cinerea</em> in grapes. The results showed that RBH primed a defense mechanism in grape berries and enhanced their response to fungal infection. RBH upregulated the expression of a group of genes involved in SA synthesis, thus inducing SA accumulation in grapes. <em>VvTCP7</em> has high homology to <em>AtCHE</em> in Arabidopsis <em>thaliana</em> and is recognized to be a nucleus-localized protein that promotes SA synthesis. Notably, RBH elevated <em>VvTCP7</em> expression in harvested grape berries, which was accompanied by enhanced expression of <em>VvNPR1</em>, a master regulator of SAR, as well as the SA-responsive <em>PR</em> genes. Additionally, Y1H, EMSA and DLR assays confirmed that VvTCP7 has the ability to bind directly to the GGNCCC motif within the <em>VvICS</em> promoter to induce <em>VvICS</em> transcription and SA synthesis. Overexpression of VvTCP7 in Arabidopsis led to a marked increase in the transcription of <em>PR</em> genes, enhancing defensive response to <em>B. cinerea</em>. However, the VvTCP7 knockout led to a decrease in <em>PR</em> gene expression and increased susceptibility to the fungus. Collectively, the data suggest that VvTCP7 contributes to RBH-induced SAR priming by activating the SA synthesis and resultant enhances SAR defenses to combat fungal invasion.</div></div>\",\"PeriodicalId\":20234,\"journal\":{\"name\":\"Plant Physiology and Biochemistry\",\"volume\":\"225 \",\"pages\":\"Article 110026\"},\"PeriodicalIF\":6.1000,\"publicationDate\":\"2025-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Physiology and Biochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0981942825005546\",\"RegionNum\":2,\"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 and Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0981942825005546","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Critical role of TCP7 in mediating RBH-induced fungal resistance in postharvest grape berries
(R)-β-homoserine (RBH) is a structural analogue of β-aminobutyric acid (BABA) that can enhance plant resistance to a wide range of pathogens. Here, we investigated the regulatory role of VvTCP7 on the RBH-induced priming response against Botrytis cinerea in grapes. The results showed that RBH primed a defense mechanism in grape berries and enhanced their response to fungal infection. RBH upregulated the expression of a group of genes involved in SA synthesis, thus inducing SA accumulation in grapes. VvTCP7 has high homology to AtCHE in Arabidopsis thaliana and is recognized to be a nucleus-localized protein that promotes SA synthesis. Notably, RBH elevated VvTCP7 expression in harvested grape berries, which was accompanied by enhanced expression of VvNPR1, a master regulator of SAR, as well as the SA-responsive PR genes. Additionally, Y1H, EMSA and DLR assays confirmed that VvTCP7 has the ability to bind directly to the GGNCCC motif within the VvICS promoter to induce VvICS transcription and SA synthesis. Overexpression of VvTCP7 in Arabidopsis led to a marked increase in the transcription of PR genes, enhancing defensive response to B. cinerea. However, the VvTCP7 knockout led to a decrease in PR gene expression and increased susceptibility to the fungus. Collectively, the data suggest that VvTCP7 contributes to RBH-induced SAR priming by activating the SA synthesis and resultant enhances SAR defenses to combat fungal invasion.
期刊介绍:
Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement.
Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB.
Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.