CPK28 介导的磷酸化增强了 NRT2.1 在氮缺乏时的硝酸盐转运活性

IF 8.3 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2024-11-02 DOI:10.1111/nph.20236
Lindi Yue, Mengyuan Liu, Jiahui Liao, Kaina Zhang, Wei‐Hua Wu, Yang Wang
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引用次数: 0

摘要

摘要 硝酸(NO3-)是大多数陆生植物吸收的主要无机氮源。硝酸盐转运体(NRTs)有助于从土壤中获取硝酸盐,其中 NRT2.1 是关键的高亲和性硝酸盐转运体。NRT2.1 有多个潜在的磷酸化位点,其活性在各种生理条件下受到复杂的调控。在这里,我们发现钙独立蛋白激酶 28(CPK28)能在缺氮条件下积极调节硝酸盐的吸收。我们通过免疫沉淀和质谱分析发现 CPK28 是激酶的靶标,并利用基于质谱的定量磷酸化蛋白质组学研究了 cpk28 突变体植物中 NRT2.1 的植株内磷酸化状态。通过体外磷酸化实验和使用磷酸化特异性抗体进行免疫印迹,我们成功地证明了 CPK28 能特异性地使 NRT2.1 在 Ser21 处磷酸化。在爪蟾卵母细胞中进行的功能分析显示,共表达 CPK28 能显著增强 NRT2.1 对硝酸盐的高亲和性吸收。利用转基因植物进行的进一步研究表明,拟磷酸化变体 NRT2.1S21E,而非非磷酸化变体 NRT2.1S21A,能完全恢复 nrt2.1 和 cpk28 突变体背景下的高亲和性 15NO3 吸收能力。这项研究明确了 CPK28 的激酶活性在缺氮条件下得到了促进。这些重要发现为研究硝酸盐需求适应性的复杂调控机制提供了宝贵的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CPK28‐mediated phosphorylation enhances nitrate transport activity of NRT2.1 during nitrogen deprivation
Summary Nitrate (NO3) serves as the primary inorganic nitrogen source assimilated by most terrestrial plants. The acquisition of nitrate from the soil is facilitated by NITRATE TRANSPORTERS (NRTs), with NRT2.1 being the key high‐affinity nitrate transporter. The activity of NRT2.1, which has multiple potential phosphorylation sites, is intricately regulated under various physiological conditions. Here, we discovered that CALCIUM‐DEPENDENT PROTEIN KINASE 28 (CPK28) positively regulates nitrate uptake under nitrogen deprivation conditions. We found CPK28 as the kinase targeted by immunoprecipitation followed by mass spectrometry and examined the in‐planta phosphorylation status of NRT2.1 in cpk28 mutant plants by employing quantitative MS‐based phosphoproteomics. Through a combination of in vitro phosphorylation experiment and immunoblotting using phospho‐specific antibody, we successfully demonstrated that CPK28 specifically phosphorylates NRT2.1 at Ser21. Functional analysis conducted in Xenopus oocytes revealed that co‐expression of CPK28 significantly enhanced high‐affinity nitrate uptake of NRT2.1. Further investigation using transgenic plants showed that the phosphomimic variant NRT2.1S21E, but not the nonphosphorylatable variant NRT2.1S21A, fully restored high‐affinity 15NO3 uptake ability in both nrt2.1 and cpk28 mutant backgrounds. This study clarifies that the kinase activity of CPK28 is promoted during nitrogen deprivation conditions. These significant findings provide valuable insights into the intricate regulatory mechanisms that govern nitrate‐demand adaptation.
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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