CPK28‐mediated phosphorylation enhances nitrate transport activity of NRT2.1 during nitrogen deprivation.

Bibliographic Details
Title: CPK28‐mediated phosphorylation enhances nitrate transport activity of NRT2.1 during nitrogen deprivation.
Authors: Yue, Lindi, Liu, Mengyuan, Liao, Jiahui, Zhang, Kaina, Wu, Wei‐Hua, Wang, Yang
Source: New Phytologist; Jan2025, Vol. 245 Issue 1, p249-262, 14p
Subject Terms: CARRIER proteins, PROTEIN kinases, TRANSGENIC plants, MASS spectrometry, PHOSPHORYLATION, NITRATE reductase
Abstract: 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. [ABSTRACT FROM AUTHOR]
Copyright of New Phytologist is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index
More Details
ISSN:0028646X
DOI:10.1111/nph.20236
Published in:New Phytologist
Language:English