Yusuf Genc, Ute Baumann, Judy Cheong, Julian Taylor, Judith Atieno, James Walter, Tristan Coram, Julie E Hayes, Tim Sutton
{"title":"自发性末端缺失导致的HKT1;5D缺失可提高面包小麦叶片钠含量,但与产量或耐盐性无关。","authors":"Yusuf Genc, Ute Baumann, Judy Cheong, Julian Taylor, Judith Atieno, James Walter, Tristan Coram, Julie E Hayes, Tim Sutton","doi":"10.1093/jxb/eraf213","DOIUrl":null,"url":null,"abstract":"<p><p>Soil salinity is a significant constraint to global wheat production, and breeding for salinity tolerance offers a sustainable solution. MW#293 is a recently developed bread wheat line, notable for both its high salinity tolerance and unusually high leaf sodium (Na⁺) accumulation. However, the association between high Na⁺ accumulation and salinity tolerance in this line was unknown. Using genetic, genomic, physiological, and agronomic approaches, we identified and delineated a terminal deletion on chromosome 4D encompassing the major Na⁺ transporter gene TaHKT1;5D and determined this as the cause of the elevated leaf Na⁺ in MW#293. In a Mace x MW#293 segregating population, leaf Na+ and shoot growth measured under salinity were shown to be under separate genetic control. Field trials were conducted in three environments ranging from slightly to moderately saline. Despite the deletion encompassing at least 286 genes, we observed neither a positive nor a negative influence on grain yield. These results suggest that TaHKT1;5D is not a critical determinant of salinity tolerance in MW#293 and related bread wheat germplasm, but that other mechanisms are responsible.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Loss of HKT1;5D via a spontaneous terminal deletion elevates leaf sodium in bread wheat, but is independent of yield or salinity tolerance.\",\"authors\":\"Yusuf Genc, Ute Baumann, Judy Cheong, Julian Taylor, Judith Atieno, James Walter, Tristan Coram, Julie E Hayes, Tim Sutton\",\"doi\":\"10.1093/jxb/eraf213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Soil salinity is a significant constraint to global wheat production, and breeding for salinity tolerance offers a sustainable solution. MW#293 is a recently developed bread wheat line, notable for both its high salinity tolerance and unusually high leaf sodium (Na⁺) accumulation. However, the association between high Na⁺ accumulation and salinity tolerance in this line was unknown. Using genetic, genomic, physiological, and agronomic approaches, we identified and delineated a terminal deletion on chromosome 4D encompassing the major Na⁺ transporter gene TaHKT1;5D and determined this as the cause of the elevated leaf Na⁺ in MW#293. In a Mace x MW#293 segregating population, leaf Na+ and shoot growth measured under salinity were shown to be under separate genetic control. Field trials were conducted in three environments ranging from slightly to moderately saline. Despite the deletion encompassing at least 286 genes, we observed neither a positive nor a negative influence on grain yield. These results suggest that TaHKT1;5D is not a critical determinant of salinity tolerance in MW#293 and related bread wheat germplasm, but that other mechanisms are responsible.</p>\",\"PeriodicalId\":15820,\"journal\":{\"name\":\"Journal of Experimental Botany\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2025-05-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Experimental Botany\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/jxb/eraf213\",\"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":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/eraf213","RegionNum":2,"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
土壤盐分是全球小麦生产的重要制约因素,耐盐育种提供了一个可持续的解决方案。MW#293是最近开发的面包小麦品系,以其高耐盐性和异常高的叶片钠(Na⁺)积累而闻名。然而,这条线中Na⁺的高积累与耐盐性之间的关系尚不清楚。利用遗传学、基因组学、生理学和农艺方法,我们确定并描绘了4D染色体上包含Na⁺主要转运体基因TaHKT1;5D的末端缺失,并确定这是导致MW#293中Na⁺含量升高的原因。在Mace x MW#293分离群体中,叶片Na+和芽部生长在盐度条件下分别受遗传控制。现场试验在三种环境中进行,从轻度到中度盐水。尽管缺失至少包含286个基因,但我们没有观察到对粮食产量的积极或消极影响。这些结果表明TaHKT1;5D不是mw# 293和相关面包小麦种质耐盐性的关键决定因素,而是其他机制起作用。
Loss of HKT1;5D via a spontaneous terminal deletion elevates leaf sodium in bread wheat, but is independent of yield or salinity tolerance.
Soil salinity is a significant constraint to global wheat production, and breeding for salinity tolerance offers a sustainable solution. MW#293 is a recently developed bread wheat line, notable for both its high salinity tolerance and unusually high leaf sodium (Na⁺) accumulation. However, the association between high Na⁺ accumulation and salinity tolerance in this line was unknown. Using genetic, genomic, physiological, and agronomic approaches, we identified and delineated a terminal deletion on chromosome 4D encompassing the major Na⁺ transporter gene TaHKT1;5D and determined this as the cause of the elevated leaf Na⁺ in MW#293. In a Mace x MW#293 segregating population, leaf Na+ and shoot growth measured under salinity were shown to be under separate genetic control. Field trials were conducted in three environments ranging from slightly to moderately saline. Despite the deletion encompassing at least 286 genes, we observed neither a positive nor a negative influence on grain yield. These results suggest that TaHKT1;5D is not a critical determinant of salinity tolerance in MW#293 and related bread wheat germplasm, but that other mechanisms are responsible.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.