{"title":"磷酸盐转运体 OsPT4 被 E3 连接酶 OsAIRP2 泛素化,在发芽种子的磷和氮转运及消耗中发挥关键作用。","authors":"Yafei Sun, Fang Zhang, Jia Wei, Ke Song, Lijuan Sun, Yang Yang, Qin Qin, Shiyan Yang, Zhouwen Li, Guohua Xu, Shubin Sun, Yong Xue","doi":"10.1186/s12284-023-00666-9","DOIUrl":null,"url":null,"abstract":"<p><p>Phosphorus (P) and nitrogen (N) are essential macronutrients necessary for plant growth and development. OsPT4 is a high-affinity phosphate (Pi) transporter that has a positive impact on nutrient uptake and seed development. In this study, the expression patterns of different Pi transporter genes in germinating seeds were determined, and the relative expression of OsPT4 was induced in Pi-deficient seeds and gradually increased with the passage of germination time. The analysis of P, N, Pi, and amino acid concentrations in germinating seeds of OsPT4 mutants showed that the OsPT4 mutation caused P and N retention and a continuous reduction in multiple amino acid concentrations in germinating seeds. Transcriptome analysis and qRT-PCR results also indicated that the OsPT4 mutation inhibits the expression of genes related to P and N transportation and amino acid synthesis in germinating seeds. In addition, the paraffin section and TUNEL assay of OsPT4 mutant germinating seeds suggests that OsPT4 mutation causes programmed cell death (PCD) delayed in the aleurone layer and inhibition of leaf outgrowth. Moreover, we also found that OsPT4 was ubiquitinated by OsAIRP2, which is a C3HC4-type RING E3 Ub ligase. Our studies illustrate that OsPT4 plays a crucial role in P and N collaborative translocation and consumption in germinating seeds. It also provides a theoretical basis for the molecules and physiological mechanisms of P and N cross-talk under suppressed Pi uptake conditions.</p>","PeriodicalId":21408,"journal":{"name":"Rice","volume":"16 1","pages":"54"},"PeriodicalIF":4.8000,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10697913/pdf/","citationCount":"0","resultStr":"{\"title\":\"Phosphate Transporter OsPT4, Ubiquitinated by E3 Ligase OsAIRP2, Plays a Crucial Role in Phosphorus and Nitrogen Translocation and Consumption in Germinating Seed.\",\"authors\":\"Yafei Sun, Fang Zhang, Jia Wei, Ke Song, Lijuan Sun, Yang Yang, Qin Qin, Shiyan Yang, Zhouwen Li, Guohua Xu, Shubin Sun, Yong Xue\",\"doi\":\"10.1186/s12284-023-00666-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Phosphorus (P) and nitrogen (N) are essential macronutrients necessary for plant growth and development. OsPT4 is a high-affinity phosphate (Pi) transporter that has a positive impact on nutrient uptake and seed development. In this study, the expression patterns of different Pi transporter genes in germinating seeds were determined, and the relative expression of OsPT4 was induced in Pi-deficient seeds and gradually increased with the passage of germination time. The analysis of P, N, Pi, and amino acid concentrations in germinating seeds of OsPT4 mutants showed that the OsPT4 mutation caused P and N retention and a continuous reduction in multiple amino acid concentrations in germinating seeds. Transcriptome analysis and qRT-PCR results also indicated that the OsPT4 mutation inhibits the expression of genes related to P and N transportation and amino acid synthesis in germinating seeds. In addition, the paraffin section and TUNEL assay of OsPT4 mutant germinating seeds suggests that OsPT4 mutation causes programmed cell death (PCD) delayed in the aleurone layer and inhibition of leaf outgrowth. Moreover, we also found that OsPT4 was ubiquitinated by OsAIRP2, which is a C3HC4-type RING E3 Ub ligase. Our studies illustrate that OsPT4 plays a crucial role in P and N collaborative translocation and consumption in germinating seeds. 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引用次数: 0
摘要
磷(P)和氮(N)是植物生长和发育所必需的重要营养元素。OsPT4 是一种高亲和性磷酸盐(Pi)转运体,对养分吸收和种子发育有积极影响。本研究测定了不同 Pi 转运体基因在萌发种子中的表达模式,发现 OsPT4 的相对表达在缺 Pi- 的种子中被诱导,并随着萌发时间的延长而逐渐增加。对 OsPT4 突变体萌发种子中 P、N、Pi 和氨基酸浓度的分析表明,OsPT4 突变导致萌发种子中 P 和 N 的保留以及多种氨基酸浓度的持续降低。转录组分析和 qRT-PCR 结果也表明,OsPT4 突变抑制了萌发种子中 P、N 运输和氨基酸合成相关基因的表达。此外,OsPT4突变体萌发种子的石蜡切片和TUNEL检测结果表明,OsPT4突变导致胚乳层程序性细胞死亡(PCD)延迟,抑制了叶片的萌发。此外,我们还发现 OsPT4 被 OsAIRP2 泛素化,而 OsAIRP2 是一种 C3HC4 型 RING E3 Ub 连接酶。我们的研究表明,OsPT4 在种子萌发过程中的 P 和 N 协同转运和消耗中起着至关重要的作用。这也为抑制π吸收条件下P和N交叉作用的分子和生理机制提供了理论依据。
Phosphate Transporter OsPT4, Ubiquitinated by E3 Ligase OsAIRP2, Plays a Crucial Role in Phosphorus and Nitrogen Translocation and Consumption in Germinating Seed.
Phosphorus (P) and nitrogen (N) are essential macronutrients necessary for plant growth and development. OsPT4 is a high-affinity phosphate (Pi) transporter that has a positive impact on nutrient uptake and seed development. In this study, the expression patterns of different Pi transporter genes in germinating seeds were determined, and the relative expression of OsPT4 was induced in Pi-deficient seeds and gradually increased with the passage of germination time. The analysis of P, N, Pi, and amino acid concentrations in germinating seeds of OsPT4 mutants showed that the OsPT4 mutation caused P and N retention and a continuous reduction in multiple amino acid concentrations in germinating seeds. Transcriptome analysis and qRT-PCR results also indicated that the OsPT4 mutation inhibits the expression of genes related to P and N transportation and amino acid synthesis in germinating seeds. In addition, the paraffin section and TUNEL assay of OsPT4 mutant germinating seeds suggests that OsPT4 mutation causes programmed cell death (PCD) delayed in the aleurone layer and inhibition of leaf outgrowth. Moreover, we also found that OsPT4 was ubiquitinated by OsAIRP2, which is a C3HC4-type RING E3 Ub ligase. Our studies illustrate that OsPT4 plays a crucial role in P and N collaborative translocation and consumption in germinating seeds. It also provides a theoretical basis for the molecules and physiological mechanisms of P and N cross-talk under suppressed Pi uptake conditions.
期刊介绍:
Rice aims to fill a glaring void in basic and applied plant science journal publishing. This journal is the world''s only high-quality serial publication for reporting current advances in rice genetics, structural and functional genomics, comparative genomics, molecular biology and physiology, molecular breeding and comparative biology. Rice welcomes review articles and original papers in all of the aforementioned areas and serves as the primary source of newly published information for researchers and students in rice and related research.