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Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2
BACKGROUND: The availability of potassium is one of the main environmental factors for modifying the plasticity of root architecture. Many potassium channels and transporters are involved in regulating primary root growth in response to low potassium stress. NRT1.5/NPF7.3 transporter is a NO(3)(−)/H...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264542/ https://www.ncbi.nlm.nih.gov/pubmed/35804293 http://dx.doi.org/10.1186/s12870-022-03730-6 |
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author | Wang, Youyou Wang, Ran Zhao, Shuang Lu, Changmei Zhu, Ziqiang Li, Hong |
author_facet | Wang, Youyou Wang, Ran Zhao, Shuang Lu, Changmei Zhu, Ziqiang Li, Hong |
author_sort | Wang, Youyou |
collection | PubMed |
description | BACKGROUND: The availability of potassium is one of the main environmental factors for modifying the plasticity of root architecture. Many potassium channels and transporters are involved in regulating primary root growth in response to low potassium stress. NRT1.5/NPF7.3 transporter is a NO(3)(−)/H(+) and K(+)/H(+) cotransporter, and participates in NO(3)(−) and K(+) translocation from the roots to the shoots. However, the underlying mechanism of NRT1.5-regulated primary root growth under low potassium stress is unclear. RESULTS: We show that NRT1.5/NPF7.3 inhibited primary root growth under low potassium conditions by regulating the accumulation of PIN2 protein and auxin levels. Under low potassium conditions, the mutants nrt1.5 and lks2 exhibited longer primary roots, longer meristem regions and elongation zones of primary roots, and more cell activity in the meristem region compared to WT plants, revealing the involvement of NRT1.5 in LK (low potassium)-inhibition primary root growth. In addition, exogenous auxin (IAA), auxin analogue (NAA, 2.4-D) or auxin precursor (IBA) promoted the primary root growth of WT and the complementation line NRT1.5 COM plants. In addition, the application of NPA inhibited the primary root growth of the nrt1.5 and lks2 mutants. Auxin accumulation was higher in the root tip of nrt1.5 plants than in WT plants, indicating that NRT1.5 regulates root growth inhibition by regulating auxin distribution. Furthermore, PIN2 was degraded more quickly in nrt1.5 plants under LK stress. CONCLUSIONS: Our findings reveal that NRT1.5 inhibits primary root growth by modulating the auxin level in the root tip via the degradation of PIN2. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03730-6. |
format | Online Article Text |
id | pubmed-9264542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92645422022-07-09 Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 Wang, Youyou Wang, Ran Zhao, Shuang Lu, Changmei Zhu, Ziqiang Li, Hong BMC Plant Biol Research BACKGROUND: The availability of potassium is one of the main environmental factors for modifying the plasticity of root architecture. Many potassium channels and transporters are involved in regulating primary root growth in response to low potassium stress. NRT1.5/NPF7.3 transporter is a NO(3)(−)/H(+) and K(+)/H(+) cotransporter, and participates in NO(3)(−) and K(+) translocation from the roots to the shoots. However, the underlying mechanism of NRT1.5-regulated primary root growth under low potassium stress is unclear. RESULTS: We show that NRT1.5/NPF7.3 inhibited primary root growth under low potassium conditions by regulating the accumulation of PIN2 protein and auxin levels. Under low potassium conditions, the mutants nrt1.5 and lks2 exhibited longer primary roots, longer meristem regions and elongation zones of primary roots, and more cell activity in the meristem region compared to WT plants, revealing the involvement of NRT1.5 in LK (low potassium)-inhibition primary root growth. In addition, exogenous auxin (IAA), auxin analogue (NAA, 2.4-D) or auxin precursor (IBA) promoted the primary root growth of WT and the complementation line NRT1.5 COM plants. In addition, the application of NPA inhibited the primary root growth of the nrt1.5 and lks2 mutants. Auxin accumulation was higher in the root tip of nrt1.5 plants than in WT plants, indicating that NRT1.5 regulates root growth inhibition by regulating auxin distribution. Furthermore, PIN2 was degraded more quickly in nrt1.5 plants under LK stress. CONCLUSIONS: Our findings reveal that NRT1.5 inhibits primary root growth by modulating the auxin level in the root tip via the degradation of PIN2. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03730-6. BioMed Central 2022-07-08 /pmc/articles/PMC9264542/ /pubmed/35804293 http://dx.doi.org/10.1186/s12870-022-03730-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Youyou Wang, Ran Zhao, Shuang Lu, Changmei Zhu, Ziqiang Li, Hong Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title | Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title_full | Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title_fullStr | Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title_full_unstemmed | Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title_short | Transporter NRT1.5/NPF7.3 suppresses primary root growth under low K(+) stress by regulating the degradation of PIN-FORMED2 |
title_sort | transporter nrt1.5/npf7.3 suppresses primary root growth under low k(+) stress by regulating the degradation of pin-formed2 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264542/ https://www.ncbi.nlm.nih.gov/pubmed/35804293 http://dx.doi.org/10.1186/s12870-022-03730-6 |
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