{"title":"Sulfur in dialogue with phosphorus, nitrogen, and iron: regulatory networks in plant nutrient homeostasis.","authors":"Afm Mohabubul Haque, Hideki Takahashi, Hatem Rouached","doi":"10.1093/jxb/erag119","DOIUrl":null,"url":null,"abstract":"<p><p>Sulfur (S) is an essential macronutrient for plant growth and resilience. The S-amino acids cysteine (Cys) and methionine (Met) are indispensable for protein synthesis and structural integrity, as well as redox homeostasis and cofactor assembly. Over the past several decades, biochemical and molecular genetic studies demonstrated the core steps in sulfate uptake and assimilation pathways, while it has become increasingly evident that S homeostasis in plants cannot be understood in isolation. Robust and reciprocal regulatory interactions link S with phosphorus (P), nitrogen (N), and iron (Fe). Plants remodel membrane lipid compositions, replacing the phospholipids with sulfolipids under P deficiency. Cys/Met biosynthesis is coordinated with N metabolism. The Fe-S cluster assembly requires a balanced supply of Fe and S. These interactions are orchestrated through shared regulatory circuits and specific hub-regulatory transcription factors, including SULFUR LIMITATION 1, PHOSPHATE STARVATION RESPONSE 1, NIN-LIKE PROTEIN 7, and FER-LIKE IRON DEFICIENCY-INDUCED FACTOR. Comparative studies reveal both species-specific and evolutionarily conserved regulatory networks. This review focuses on mechanistic insights into the regulatory circuits revealed from studies with the model plant Arabidopsis thaliana, where the genetic and molecular resolution enabled detailed dissection of the signaling and regulatory networks. This review also highlights unresolved mechanistic gaps and provides insights into systems-level understanding and potential translational approaches that can be implemented to improve crop nutrient use efficiency and stress resilience.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":"6048-6061"},"PeriodicalIF":6.5000,"publicationDate":"2026-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13621317/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/erag119","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
Abstract
Sulfur (S) is an essential macronutrient for plant growth and resilience. The S-amino acids cysteine (Cys) and methionine (Met) are indispensable for protein synthesis and structural integrity, as well as redox homeostasis and cofactor assembly. Over the past several decades, biochemical and molecular genetic studies demonstrated the core steps in sulfate uptake and assimilation pathways, while it has become increasingly evident that S homeostasis in plants cannot be understood in isolation. Robust and reciprocal regulatory interactions link S with phosphorus (P), nitrogen (N), and iron (Fe). Plants remodel membrane lipid compositions, replacing the phospholipids with sulfolipids under P deficiency. Cys/Met biosynthesis is coordinated with N metabolism. The Fe-S cluster assembly requires a balanced supply of Fe and S. These interactions are orchestrated through shared regulatory circuits and specific hub-regulatory transcription factors, including SULFUR LIMITATION 1, PHOSPHATE STARVATION RESPONSE 1, NIN-LIKE PROTEIN 7, and FER-LIKE IRON DEFICIENCY-INDUCED FACTOR. Comparative studies reveal both species-specific and evolutionarily conserved regulatory networks. This review focuses on mechanistic insights into the regulatory circuits revealed from studies with the model plant Arabidopsis thaliana, where the genetic and molecular resolution enabled detailed dissection of the signaling and regulatory networks. This review also highlights unresolved mechanistic gaps and provides insights into systems-level understanding and potential translational approaches that can be implemented to improve crop nutrient use efficiency and stress resilience.
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.