{"title":"SnRK2-HAK调控模块赋予玉米耐盐性自然变异","authors":"Ming Zhang, Xueyan Zhou, Limin Wang, Xiaoyan Liang, Xin Liu, Caifu Jiang","doi":"10.1038/s41467-025-59332-x","DOIUrl":null,"url":null,"abstract":"<p>The exclusion of sodium ions (Na<sup>+</sup>) from the shoot tissue, termed shoot Na<sup>+</sup> exclusion, underlies a core mechanism of crop salt tolerance. Recent studies have shown that the HAK (High-Affinity K<sup>+</sup> Transporter) family Na<sup>+</sup> transporters play a key role in shoot Na<sup>+</sup> exclusion of various crops, however, it is unknown whether and how this type of transporter is post-transcriptionally regulated. Here, we show that two closely related SnRK2 kinases, designated as ZmSnRK2.9 and ZmSnRK2.10, promote shoot Na<sup>+</sup> exclusion and salt tolerance by activating the Na<sup>+</sup> transporter ZmHAK4 in maize. Under salt conditions, the kinase activity of ZmSnRK2.9 and ZmSnRK2.10 is activated, then they interact with and phosphorylate ZmHAK4 at Ser5, increasing the Na<sup>+</sup> transport activity of ZmHAK4, which in turn promotes salt tolerance by improving the exclusion of Na<sup>+</sup> from the shoot tissue. Furthermore, we show that a 20-bp deletion that occurred naturally in the <i>ZmSnRK2.10</i> promoter decreases its transcript level, resulting in an increased shoot Na<sup>+</sup> content under salt conditions. Our findings support a breeding program that can utilize the favorable alleles of <i>ZmHAK4</i> and <i>ZmSnRK2.10</i> to enhance both the transcriptional and post-transcriptional activation of ZmHAK4, thus advancing the development of salt-tolerant maize.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"24 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A SnRK2-HAK regulatory module confers natural variation of salt tolerance in maize\",\"authors\":\"Ming Zhang, Xueyan Zhou, Limin Wang, Xiaoyan Liang, Xin Liu, Caifu Jiang\",\"doi\":\"10.1038/s41467-025-59332-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The exclusion of sodium ions (Na<sup>+</sup>) from the shoot tissue, termed shoot Na<sup>+</sup> exclusion, underlies a core mechanism of crop salt tolerance. Recent studies have shown that the HAK (High-Affinity K<sup>+</sup> Transporter) family Na<sup>+</sup> transporters play a key role in shoot Na<sup>+</sup> exclusion of various crops, however, it is unknown whether and how this type of transporter is post-transcriptionally regulated. Here, we show that two closely related SnRK2 kinases, designated as ZmSnRK2.9 and ZmSnRK2.10, promote shoot Na<sup>+</sup> exclusion and salt tolerance by activating the Na<sup>+</sup> transporter ZmHAK4 in maize. Under salt conditions, the kinase activity of ZmSnRK2.9 and ZmSnRK2.10 is activated, then they interact with and phosphorylate ZmHAK4 at Ser5, increasing the Na<sup>+</sup> transport activity of ZmHAK4, which in turn promotes salt tolerance by improving the exclusion of Na<sup>+</sup> from the shoot tissue. Furthermore, we show that a 20-bp deletion that occurred naturally in the <i>ZmSnRK2.10</i> promoter decreases its transcript level, resulting in an increased shoot Na<sup>+</sup> content under salt conditions. Our findings support a breeding program that can utilize the favorable alleles of <i>ZmHAK4</i> and <i>ZmSnRK2.10</i> to enhance both the transcriptional and post-transcriptional activation of ZmHAK4, thus advancing the development of salt-tolerant maize.</p>\",\"PeriodicalId\":19066,\"journal\":{\"name\":\"Nature Communications\",\"volume\":\"24 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-04-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature Communications\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1038/s41467-025-59332-x\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-59332-x","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
A SnRK2-HAK regulatory module confers natural variation of salt tolerance in maize
The exclusion of sodium ions (Na+) from the shoot tissue, termed shoot Na+ exclusion, underlies a core mechanism of crop salt tolerance. Recent studies have shown that the HAK (High-Affinity K+ Transporter) family Na+ transporters play a key role in shoot Na+ exclusion of various crops, however, it is unknown whether and how this type of transporter is post-transcriptionally regulated. Here, we show that two closely related SnRK2 kinases, designated as ZmSnRK2.9 and ZmSnRK2.10, promote shoot Na+ exclusion and salt tolerance by activating the Na+ transporter ZmHAK4 in maize. Under salt conditions, the kinase activity of ZmSnRK2.9 and ZmSnRK2.10 is activated, then they interact with and phosphorylate ZmHAK4 at Ser5, increasing the Na+ transport activity of ZmHAK4, which in turn promotes salt tolerance by improving the exclusion of Na+ from the shoot tissue. Furthermore, we show that a 20-bp deletion that occurred naturally in the ZmSnRK2.10 promoter decreases its transcript level, resulting in an increased shoot Na+ content under salt conditions. Our findings support a breeding program that can utilize the favorable alleles of ZmHAK4 and ZmSnRK2.10 to enhance both the transcriptional and post-transcriptional activation of ZmHAK4, thus advancing the development of salt-tolerant maize.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.