{"title":"乙烯部分通过VvERF1B-VvMYC2-VvPMA10途径提高葡萄耐NaHCO3胁迫能力","authors":"Guangqing Xiang, Zongbao Fan, Shuxia Lan, Dezheng Wei, Yazhe Gao, Hui Kang, Yuxin Yao","doi":"10.1111/pbi.14565","DOIUrl":null,"url":null,"abstract":"Here, we evaluated the role of ethylene in regulating the NaHCO<sub>3</sub> stress tolerance of grapevines and clarified the mechanism by which <i>VvERF1B</i> regulates the response to NaHCO<sub>3</sub> stress. The exogenous application of ACC and <i>VvACS3</i> overexpression in grapevines and grape calli revealed that ethylene increased NaHCO<sub>3</sub> stress tolerance, and this was accompanied by increased plasma membrane H<sup>+</sup>-ATPase (PMA) activity. The expression of <i>VvERF1B</i> was strongly induced by ACC, and overexpression of this gene in grapevines conferred increased NaHCO<sub>3</sub> stress tolerance and enhanced PMA activity and H<sup>+</sup> and oxalate secretion. Additionally, the function of <i>VvERF1B</i> was also verified using mutant transgenic grape calli and overexpression in <i>Arabidopsis</i> plants. The expression of <i>VvPMA10</i> was strongly induced following the overexpression of <i>VvERF1B</i> in grapevine roots, and <i>VvPMA10</i> was shown to regulate PMA activity, oxalate and H<sup>+</sup> secretion, and NaHCO<sub>3</sub> stress tolerance via its overexpression and mutation in grapevine roots, calli, and/or <i>Arabidopsis</i>. However, <i>VvPMA10</i> was not a direct target gene of VvERF1B but was directly transactivated by VvMYC2. The function of <i>VvMYC2</i> was shown to be similar to that of <i>VvPMA10</i> via its overexpression and mutation in grape calli. Additional experiments revealed that the interaction of VvERF1B with VvMYC2 increased its ability to activate <i>VvPMA10</i> expression and that VvMYC2 played a role in the VvERF1B-mediated pathway. Overall, the VvERF1B-VvMYC2-VvPMA pathway played a role in regulating ethylene-induced NaHCO<sub>3</sub> stress tolerance in grapevines, and this process contributed to increases in PMA activity and H<sup>+</sup> and oxalate secretion.","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":"79 1","pages":""},"PeriodicalIF":10.1000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ethylene increases the NaHCO3 stress tolerance of grapevines partially via the VvERF1B-VvMYC2-VvPMA10 pathway\",\"authors\":\"Guangqing Xiang, Zongbao Fan, Shuxia Lan, Dezheng Wei, Yazhe Gao, Hui Kang, Yuxin Yao\",\"doi\":\"10.1111/pbi.14565\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Here, we evaluated the role of ethylene in regulating the NaHCO<sub>3</sub> stress tolerance of grapevines and clarified the mechanism by which <i>VvERF1B</i> regulates the response to NaHCO<sub>3</sub> stress. The exogenous application of ACC and <i>VvACS3</i> overexpression in grapevines and grape calli revealed that ethylene increased NaHCO<sub>3</sub> stress tolerance, and this was accompanied by increased plasma membrane H<sup>+</sup>-ATPase (PMA) activity. The expression of <i>VvERF1B</i> was strongly induced by ACC, and overexpression of this gene in grapevines conferred increased NaHCO<sub>3</sub> stress tolerance and enhanced PMA activity and H<sup>+</sup> and oxalate secretion. Additionally, the function of <i>VvERF1B</i> was also verified using mutant transgenic grape calli and overexpression in <i>Arabidopsis</i> plants. The expression of <i>VvPMA10</i> was strongly induced following the overexpression of <i>VvERF1B</i> in grapevine roots, and <i>VvPMA10</i> was shown to regulate PMA activity, oxalate and H<sup>+</sup> secretion, and NaHCO<sub>3</sub> stress tolerance via its overexpression and mutation in grapevine roots, calli, and/or <i>Arabidopsis</i>. However, <i>VvPMA10</i> was not a direct target gene of VvERF1B but was directly transactivated by VvMYC2. The function of <i>VvMYC2</i> was shown to be similar to that of <i>VvPMA10</i> via its overexpression and mutation in grape calli. Additional experiments revealed that the interaction of VvERF1B with VvMYC2 increased its ability to activate <i>VvPMA10</i> expression and that VvMYC2 played a role in the VvERF1B-mediated pathway. Overall, the VvERF1B-VvMYC2-VvPMA pathway played a role in regulating ethylene-induced NaHCO<sub>3</sub> stress tolerance in grapevines, and this process contributed to increases in PMA activity and H<sup>+</sup> and oxalate secretion.\",\"PeriodicalId\":221,\"journal\":{\"name\":\"Plant Biotechnology Journal\",\"volume\":\"79 1\",\"pages\":\"\"},\"PeriodicalIF\":10.1000,\"publicationDate\":\"2025-01-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Biotechnology Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1111/pbi.14565\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/pbi.14565","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Ethylene increases the NaHCO3 stress tolerance of grapevines partially via the VvERF1B-VvMYC2-VvPMA10 pathway
Here, we evaluated the role of ethylene in regulating the NaHCO3 stress tolerance of grapevines and clarified the mechanism by which VvERF1B regulates the response to NaHCO3 stress. The exogenous application of ACC and VvACS3 overexpression in grapevines and grape calli revealed that ethylene increased NaHCO3 stress tolerance, and this was accompanied by increased plasma membrane H+-ATPase (PMA) activity. The expression of VvERF1B was strongly induced by ACC, and overexpression of this gene in grapevines conferred increased NaHCO3 stress tolerance and enhanced PMA activity and H+ and oxalate secretion. Additionally, the function of VvERF1B was also verified using mutant transgenic grape calli and overexpression in Arabidopsis plants. The expression of VvPMA10 was strongly induced following the overexpression of VvERF1B in grapevine roots, and VvPMA10 was shown to regulate PMA activity, oxalate and H+ secretion, and NaHCO3 stress tolerance via its overexpression and mutation in grapevine roots, calli, and/or Arabidopsis. However, VvPMA10 was not a direct target gene of VvERF1B but was directly transactivated by VvMYC2. The function of VvMYC2 was shown to be similar to that of VvPMA10 via its overexpression and mutation in grape calli. Additional experiments revealed that the interaction of VvERF1B with VvMYC2 increased its ability to activate VvPMA10 expression and that VvMYC2 played a role in the VvERF1B-mediated pathway. Overall, the VvERF1B-VvMYC2-VvPMA pathway played a role in regulating ethylene-induced NaHCO3 stress tolerance in grapevines, and this process contributed to increases in PMA activity and H+ and oxalate secretion.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.